METHOD FOR PRODUCING A DEUTERATED OR TRITIATED NAD(P)H
20210024970 ยท 2021-01-28
Inventors
- Kylie VINCENT (Oxford (Oxfordshire), GB)
- Holly REEVE (Oxford (Oxfordshire), GB)
- Jack ROWBOTHAM (Oxford (Oxfordshire), GB)
Cpc classification
International classification
Abstract
The invention relates to a method of producing a reduced labelled cofactor comprising one or more .sup.xH atom, wherein x is 2 or 3. The invention also relates to a method of producing a reduced labelled reaction product comprising one or more .sup.xH atom, wherein x is 2 or 3, wherein the method comprises producing a reduced labelled cofactor according to the invention. The invention also relates to systems for performing such methods.
Claims
1. A method of producing a reduced labelled cofactor comprising one or more .sup.xH atom, wherein x is 2 or 3, wherein said method comprises: i) providing a composition comprising (i) .sup.xH.sup.+ ions and (ii) an oxidised cofactor; ii) transferring electrons from an electron source to a first polypeptide which is an NADH:acceptor oxidoreductase or an NADPH:acceptor oxidoreductase or a functional derivative or fragment thereof; and iii) contacting the .sup.xH.sup.+ ions and the oxidised cofactor with the first polypeptide thereby reducing the oxidised cofactor to form a reduced labelled cofactor comprising one or more .sup.xH atoms.
2. A method of producing a reduced labelled reaction product comprising one or more .sup.xH atom, wherein x is 2 or 3, wherein said method comprises producing a reduced labelled cofactor according to claim 1; and iv) contacting the reduced labelled cofactor and an oxidised reactant with at least one enzyme that is an NADH-dependent oxidoreductase or an NADPH-dependent oxidoreductase or a functional derivative or fragment thereof such that the enzyme selectively transfers an .sup.xH atom from the reduced labelled cofactor to the oxidised reactant thereby producing a reduced labelled reaction product and an oxidised cofactor.
3. A method according to claim 2 which further comprises reducing the oxidised cofactor produced in step (iv) of claim 2 in a method according to claim 1.
4. A method according to claim 2 which comprises producing a reduced labelled reaction product according to steps (i) to (iv) of claims 1 and 2, and repeating steps (ii) to (iv) multiple times, thereby recycling the cofactor.
5. A method according to any one of the preceding claims wherein the .sup.xH.sup.+ ions are provided as .sup.2H.sub.2O or .sup.3H.sub.2O.
6. A method according to any one of the preceding claims wherein the oxidised cofactor is NAD.sup.+, NADP.sup.+, or a labelled version of NAD.sup.+ or NADP.sup.+ comprising at least one .sup.xH atom.
7. A method according to any one of the preceding claims wherein reducing the oxidised cofactor to form a reduced labelled cofactor comprises adding an .sup.xH atom at the 4-position of the nicotinamide ring of the oxidised cofactor.
8. A method according to any one of the preceding claims wherein the .sup.xH.sup.+ ions are transferred directly from the composition comprising .sup.xH.sup.+ ions to the first polypeptide.
9. A method according to any one of the preceding claims wherein the first polypeptide transfers an .sup.xH.sup. anion to the oxidised cofactor thereby forming the reduced labelled cofactor.
10. A method according to any one of the preceding claims wherein the first polypeptide comprises a flavin group.
11. A method according to any one of the preceding claims wherein the first polypeptide has a structure comprising a Rossmann fold.
12. A method according to any one of the preceding claims wherein the first polypeptide comprises or consists of a diaphorase moiety.
13. A method according to any one of the preceding claims wherein the first polypeptide consists or comprises of one or more than one of: i) the amino acid sequence of Ralstonia eutropha diaphorase HoxF (SEQ ID NO: 1) or an amino acid sequence having at least 60% homology therewith; ii) the amino acid sequence of Ralstonia eutropha diaphorase HoxU (SEQ ID NO: 2) or an amino acid sequence having at least 60% homology therewith; iii) the amino acid sequence of Ralstonia eutropha diaphorase HoxI (SEQ ID NO: 3) or an amino acid sequence having at least 60% homology therewith; iv) the amino acid sequence of the 51 kDa protein of the flavoprotein (Fp) subcomplex of Complex I of Bos taurus (SEQ ID NO: 4) or an amino acid sequence having at least 60% homology therewith; v) the amino acid sequence of the 24 kDa subcomplex of Complex I of Bos taurus (SEQ ID NO: 5) or an amino acid sequence having at least 60% homology therewith; vi) the amino acid sequence of Ralstonia eutropha NAD.sup.+-dependent formate dehydrogenase diaphorase moiety FdsB (SEQ ID NO: 6) or an amino acid sequence having at least 60% homology therewith; vii) the amino acid sequence of Ralstonia eutropha NAD.sup.+-dependent formate dehydrogenase diaphorase moiety FdsG (SEQ ID NO: 7) or an amino acid sequence having at least 60% homology therewith; viii) the amino acid sequence of Rhodobacter capsulatus NAD.sup.+-dependent formate dehydrogenase, diaphorase moiety FdsB (SEQ ID NO: 8) or an amino acid sequence having at least 60% homology therewith; ix) the amino acid sequence of Rhodobacter capsulatus NAD.sup.+-dependent formate dehydrogenase, diaphorase moiety FdsG (SEQ ID NO: 9) or an amino acid sequence having at least 60% homology therewith; x) the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase I gamma subunit (SEQ ID NO: 10) or an amino acid sequence having at least 60% homology therewith; xi) the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase I beta subunit (SEQ ID NO: 11) or an amino acid sequence having at least 60% homology therewith; xii) the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase II gamma subunit (SEQ ID NO: 12) or an amino acid sequence having at least 60% homology therewith; xiii) the amino acid sequence of the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase II beta subunit (SEQ ID NO: 13) or an amino acid sequence having at least 60% homology therewith; xiv) the amino acid sequence of the diaphorase moiety of Rhodococcus opacus soluble hydrogenase HoxF (SEQ ID NO: 14) or an amino acid sequence having at least 60% homology therewith; xv) the amino acid sequence of the diaphorase moiety of Rhodococcus opacus soluble hydrogenase HoxU (SEQ ID NO: 15) or an amino acid sequence having at least 60% homology therewith; xvi) the amino acid sequence of the diaphorase moiety of Allochromatium vinosum soluble hydrogenase HoxF (SEQ ID NO: 16) or an amino acid sequence having at least 60% homology therewith; xvii) the amino acid sequence of the diaphorase moiety of Allochromatium vinosum soluble hydrogenase HoxU (SEQ ID NO: 17) or an amino acid sequence having at least 60% homology therewith; xviii) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina Hox1F (SEQ ID NO: 18) or an amino acid sequence having at least 60% homology therewith; xix) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina soluble hydrogenase Hox1U (SEQ ID NO: 19) or an amino acid sequence having at least 60% homology therewith; xx) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina Hox2F (SEQ ID NO: 20) or an amino acid sequence having at least 60% homology therewith; xxi) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina soluble hydrogenase Hox2U (SEQ ID NO: 21) or an amino acid sequence having at least 60% homology therewith; xxii) the amino acid sequence of the diaphorase moiety of Synechocystis sp. PCC 6803 HoxF (SEQ ID NO: 22) or an amino acid sequence having at least 60% homology therewith; xxiii) the amino acid sequence of the diaphorase moiety of Synechocystis sp. PCC 6803 HoxU (SEQ ID NO: 23) or an amino acid sequence having at least 60% homology therewith; xxiv) the amino acid sequence of the diaphorase moiety of Synechococcus elongatus PCC 6301 HoxF (SEQ ID NO: 24) or an amino acid sequence having at least 60% homology therewith; xxv) the amino acid sequence of the diaphorase moiety of Synechococcus elongatus PCC 6301 HoxU (SEQ ID NO: 25) or an amino acid sequence having at least 60% homology therewith; xxvi) the amino acid sequence of Hydrogenophilus thermoluteolus diaphorase HoxF (SEQ ID NO: 26) or an amino acid sequence having at least 60% homology therewith; xxvii) the amino acid sequence of Hydrogenophilus thermoluteolus diaphorase HoxU (SEQ ID NO: 27) or an amino acid sequence having at least 60% homology therewith; xxviii) the amino acid sequence of Chlamydomonas reinhardtii Ferredoxin-NADP+ reductase (SEQ ID NO: 28) or an amino acid sequence having at least 60% homology therewith; xxix) the amino acid sequence of Anabaena Ferredoxin-NADP+ reductase (SEQ ID NO: 29) or an amino acid sequence having at least 60% homology therewith; xxx) the amino acid sequence of Ralstonia eutropha diaphorase HoxF (SEQ ID NO: 70) or an amino acid sequence having at least 60% homology therewith; xxxi) the amino acid sequence of Ralstonia eutropha diaphorase with inactive hydrogenase (SEQ ID NO: 1 and/or 2 and/or 69 and/or 31) or an amino acid sequence having at least 60% homology therewith or a functional fragment, derivative or variant thereof.
14. A method according to any one of the preceding claims wherein the first polypeptide consists or comprises of the Ralstonia eutropha NAD-reducing soluble hydrogenase or a functional fragment, derivative or variant thereof.
15. A method according to any one of the preceding claims wherein the electron source comprises a second polypeptide which is an oxidising enzyme or functional derivative or fragment thereof capable of oxidising a reductant to extract electrons, wherein the second polypeptide transfers electrons from the reductant to the first polypeptide via an electronically-conducting pathway.
16. A method according to claim 15 wherein the first polypeptide and the second polypeptide constitute component parts of a modular, multidomain or multicomponent protein or protein complex.
17. A method according to any one of claims 1 to 14 wherein the electron source comprises a synthetic organic, inorganic or metallic oxidation catalyst capable of oxidising a reductant to extract electrons, wherein the oxidation catalyst transfers electrons from the reductant to the first polypeptide via an electronically-conducting pathway.
18. A method according to claim 15 or 16 wherein the second polypeptide is selected or modified to oxidise H.sub.2 or .sup.xH.sub.2 under the conditions of the method.
19. A method according to claim 18 wherein the second polypeptide is a hydrogenase enzyme or a functional derivative or fragment thereof.
20. A method according to claim 19 wherein the hydrogenase is selected from i) the amino acid sequence of Ralstonia eutropha soluble hydrogenase moiety (SEQ ID NOs: 30 and/or 31) or an amino acid sequence having at least 60% homology therewith; ii) the amino acid sequence of Ralstonia eutropha membrane-bound hydrogenase moiety (SEQ ID NOs: 32 and/or 33 and/or 34) or an amino acid sequence having at least 60% homology therewith; iii) the amino acid sequence of Ralstonia eutropha regulatory hydrogenase moiety (SEQ ID NOs: 35 and/or 36) or an amino acid sequence having at least 60% homology therewith; iv) the amino acid sequence of Escherichia coli hydrogenase 1 (SEQ ID NOs:37 and/or 38) or an amino acid sequence having at least 60% homology therewith; v) the amino acid sequence of Escherichia coli hydrogenase 2 (SEQ ID NOs:39 and/or 40) or an amino acid sequence having at least 60% homology therewith; vi) the amino acid sequence of Aquifex aeolicus hydrogenase 1 (SEQ ID NO:41 and/or 42) or an amino acid sequence having at least 60% homology therewith; vii) the amino acid sequence of Hydrogenovibrio marinus hydrogenase (SEQ ID NOs: 43 and/or 44) or an amino acid sequence having at least 60% homology therewith; viii) the amino acid sequence of Thiocapsa roseopersicina hydrogenase (SEQ ID NOs: 45 and 46) or an amino acid sequence having at least 60% homology therewith; ix) the amino acid sequence of Alteromonas macleodii hydrogenase (SEQ ID NOs: 47 and/or 48) or an amino acid sequence having at least 60% homology therewith; x) the amino acid sequence of Rhodococcus opacus soluble hydrogenase moiety (SEQ ID NOs: 49 and/or 50) or an amino acid sequence having at least 60% homology therewith; xi) the amino acid sequence of Allochromatium vinosum membrane bound hydrogenase (SEQ ID NOs: 51 and/or 52) or an amino acid sequence having at least 60% homology therewith; xii) the amino acid sequence of Desulfovibrio fructosovorans membrane bound hydrogenase (SEQ ID NOs: 53 and/or 54) or an amino acid sequence having at least 60% homology therewith; xiii) the amino acid sequence of Clostridium pasteurianum iron-iron hydrogenase (SEQ ID NOs: 55) or an amino acid sequence having at least 60% homology therewith; xiv) the amino acid sequence of Clostridium acetobutylicum iron-iron hydrogenase (SEQ ID NOs: 56) or an amino acid sequence having at least 60% homology therewith; xv) the amino acid sequence of Chlamydomonas reinhardtii iron-iron hydrogenase (SEQ ID NOs: 57) or an amino acid sequence having at least 60% homology therewith; xvi) the amino acid sequence of Desulfomicrobium baculatum nickel-iron selenium hydrogenase (SEQ ID NOs: 58 and/or 59) or an amino acid sequence having at least 60% homology therewith; xvii) the amino acid sequence of Hydrogenophilus thermoluteolus soluble hydrogenase moiety (SEQ ID NOs: 60 and/or 61) or an amino acid sequence having at least 60% homology therewith; xviii) the amino acid sequence of Desulfovibrio vulgaris Nickel Iron hydrogenase (pdb 1H2A) (SEQ ID NOs: 62 and/or 63) or an amino acid sequence having at least 60% homology therewith; xix) the amino acid sequence of Desulfovibrio gigas Periplasmic [NiFe] hydrogenase (SEQ ID NOs: 64 and/or 65) or an amino acid sequence having at least 60% homology therewith; xx) the amino acid sequence of Salmonella enterica serovar Typhimurium LT2 nickel-iron hydrogenase 5 (SEQ ID NO: 66 and/or 67) or an amino acid sequence having at least 60% homology therewith. xxi) the amino acid sequence of Pyrococcus furiosus soluble alpha subunit (SEQ ID NOs: 68) or an amino acid sequence having at least 60% homology therewith; or a functional fragment, derivative or variant thereof.
21. A method according to claim 17 wherein the oxidation catalyst comprises platinum, palladium, iridium nickel, rhodium and/or ruthenium.
22. A method according to any one of claims 15 to 21 wherein the reductant oxidised by the second polypeptide or the oxidation catalyst is H.sub.2 or .sup.xH.sub.2.
23. A method according to any one of claims 15 to 22 wherein the reductant oxidised by the second polypeptide or the oxidation catalyst is H.sub.2.
24. A method according to any one of claims 15 to 23 wherein the electron source and the first polypeptide are each in electronic contact with an electronically conducting support.
25. A method according to claim 24 wherein the electron source and the first polypeptide are each in electronic contact with the same electronically conducting support.
26. A method according to claim 25 wherein the support is an electronically conducting particle.
27. A method according to claim 24 wherein the electron source is in electronic contact with an electronically conducting first support and the first polypeptide is in electronic contact with an electronically conducting second support; and the first support is in electronic contact with the second support.
28. A method according to any one of claims 1 to 14 wherein the electron source comprises an electrode connected to an electrode controller, wherein the electrode is connected to the first polypeptide via an electronically-conducting pathway.
29. A method according to any one of claims 24 to 27 wherein the or each support comprises a material comprising carbon, a metal or metal alloy, a metal oxide or mixed metal oxide, a metal hydroxide, a metal chalcogenide, a semi-conducting material, or an electronically-conductive polymer, or mixtures thereof; or according to claim 28 wherein the electrode comprises a material comprising carbon, a metal or metal alloy, a metal oxide or mixed metal oxide, a metal hydroxide, a metal chalcogenide, or an electronically-conductive polymer, or mixtures thereof.
30. A method according to claim 29 wherein the material comprises: i) carbon; and/or ii) a metal or metal alloy selected from gold, silver, tungsten, iridium, platinum, palladium, copper, titanium, brass, and steel; and/or iii) a material selected from titanium oxide, indium oxide, tin oxide and indium tin oxide.
31. A method according to claim 29 wherein the material comprises graphite, carbon nanotube(s), carbon black, activated carbon, carbon nanopowder, vitreous carbon, carbon fibre(s), carbon cloth, carbon felt, carbon paper, graphene, highly oriented pyrolytic graphite, pyrolytic graphite, or doped diamond.
32. A method according to any one of claims 15 to 31 wherein electrons are directly transferred along the electronically-conducting pathway.
33. A method according to any one of claims 15 to 31 wherein electron transfer along the electronically-conducting pathway is mediated by one or more electron mediators.
34. A method according to any one of claims 2 to 33 wherein the at least one enzyme that is an NADH-dependent oxidoreductase or NADPH-dependent oxidoreductase is at least one of an NAD(P)H-dependent alcohol dehydrogenase, an NAD(P)H-dependent ene reductase, an NAD(P)H-dependent imine reductase or an NAD(P)H-dependent amino-acid dehydrogenase.
35. A method according to claim 34 wherein the at least one enzyme that is an NADH-dependent oxidoreductase or NADPH-dependent oxidoreductase is at least one of an alcohol dehydrogenase or an amino acid dehydrogenase.
36. A system for performing a method according to any one of claims 1 to 35, the system comprising: i) a composition comprising (i) .sup.xH.sup.+ ions wherein x is 2 or 3 and (ii) an oxidised cofactor, wherein preferably the composition is as defined in claim 5 and/or the oxidised cofactor is as defined in claim 6 or claim 7; ii) an electron source, wherein preferably the electron source is as defined in any one of claims 14 to 32; and iii) a first polypeptide which is an NADH:acceptor oxidoreductase or an NADPH:acceptor oxidoreductase or a functional derivative or fragment thereof, wherein preferably the first polypeptide is as defined in any one of claims 8 to 13; wherein the system is configured such that, in use, (a) electrons are transferred from the electron source to the first polypeptide and (b) .sup.xH.sup.+ ions and the oxidised cofactor are contacted with the first polypeptide so as to reduce the oxidised cofactor to form a reduced labelled cofactor comprising one or more .sup.xH atoms; wherein preferably the .sup.xH.sup.+ ions are transferred directly from the composition comprising .sup.xH.sup.+ ions to the first polypeptide.
36. A method for producing an oxidised labelled cofactor comprising one or more .sup.xH atom, wherein x is 2 or 3, comprising producing a reduced labelled cofactor comprising one or more .sup.xH atom according to any one of claims 1 to 35; and oxidising the reduced labelled cofactor.
Description
BRIEF DESCRIPTION OF THE FIGURES
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[0119] Pt/C=platinum supported on carbon;
[0120] Pt+NAD-R/C=platinum and NAD.sup.+ reductase supported on carbon;
[0121] H2ase+NAD-R/C=hydrogenase and NAD.sup.+ reductase supported on carbon;
[0122] soluble hydrogenase=unsupported soluble hydrogenase enzyme comprising both a first polypeptide and a second polypeptide as described herein.
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DETAILED DESCRIPTION OF THE INVENTION
[0142] Methods of the Invention
[0143] As described above, the invention provides methods for producing reduced labelled reaction products comprising one or more .sup.xH atom, wherein x is 2 or 3. In such methods, the oxidised cofactor produced in step (iv) of the method is preferably re-reduced to form a reduced labelled cofactor in accordance with the methods described herein. Preferably, the reduced labelled reaction product thus produced is subsequently oxidised and reduced multiple times in methods of the invention, thereby recycling the cofactor.
[0144] For avoidance of doubt, by recycling the cofactor, it is meant that a single cofactor molecule can be reduced in a method of the invention to form a reduced labelled cofactor. The reduced labelled cofactor can subsequently transfer a labelled hydrogen atom to an oxidised reactant to yield a reduced labelled reaction product and an oxidised cofactor, which can be re-reduced as described. The repeated reduction and oxidation of the cofactor corresponds to recycling of the cofactor. The net result is that the cofactor itself is not consumed, and the .sup.xH.sup.+ ions and electrons are consumed by the oxidised reactant in the production of reduced labelled reaction product. This method is illustrated schematically in
[0145] In methods of the invention which involve recycling the cofactor, each cofactor molecule is typically recycled as defined herein at least 10 times, such as at least 100 times, more preferably at least 1000 times e.g. at least 10,000 times or at least 100,000 times, such as at least 1,000,000 times. Accordingly, in methods of the invention, the turnover number (TN) is typically at least 10, such as at least 100, more preferably at least 1000 e.g. at least 10,000 or at least 100,000, such as at least 1,000,000. As those skilled in the art will appreciate, the TN indicates the number of moles of product generated per mole of cofactor, and is thus a measure of the number of times each cofactor molecule is used.
[0146] Enzyme turnover can be calculated in a number of ways. The Total Turnover Number (TTN, also known as the TON) is a measure of the number of moles of product per mole of enzyme (specifically per mole of the first polypeptide). Accordingly, in methods of the invention for the production of a reduced labelled cofactor, the TTN indicates the number of moles of reduced labelled cofactor generated per mole of first polypeptide. As those skilled in the art will appreciate, the TTN thus indicates the number of times that the enzyme (i.e. the first polypeptide) has turned over.
[0147] The Turnover Frequency (TOF) is a measure of the number of moles of product generated per second per mole of enzyme (first polypeptide) present. Accordingly, in methods of the invention for the production of a reduced labelled cofactor, the TTN indicates the number of moles of reduced labelled cofactor generated per second per mole of first polypeptide. Accordingly, the TOF is identified with the number of catalytic cycles undertaken by each enzyme molecule per second.
[0148] Preferably, in the methods of the invention, the first polypeptide has a TOF of 0.1 to 1000 s.sup.1, more preferably 1 to 100 s.sup.1 such as from about 10 to about 50 s.sup.1.
[0149] The composition comprising .sup.xH.sup.+ ions and oxidised cofactor typically comprises .sup.2H.sub.2O or .sup.3H.sub.2O as the source of .sup.xH.sup.+ ions; typically the composition further comprises substances such as buffers and the like, as described herein, in addition to the oxidised cofactor itself. Typically, therefore, the .sup.xH.sup.+ ions are provided as .sup.2H.sub.2O or .sup.3H.sub.2O. Those skilled in the art will appreciate that when the composition comprising H.sup.+ ions comprises both .sup.xH.sub.2O and .sup.1H.sub.2O, the .sup.xH.sup.+ ions may be present in the form of .sup.1H.sup.xHO. Those skilled in the art will appreciate that .sup.xH.sup.+ ions can be present in the form of hydrogen-containing compounds or in the form of solvated ions e.g. .sup.xH.sup.+.sub.(aq) e.g. .sup.xH.sub.3O.sup.+, .sup.1H.sub.2.sup.xHO.sup.+ or .sup.1H.sup.xH.sub.2O.sup.+. Even at neutral or alkaline pH (p.sup.xH) a non-zero concentration of .sup.xH.sup.+.sub.(aq) ions are present in aqueous solution. Of course, the composition comprising .sup.xH.sup.+ ions and oxidised cofactor may also comprise reduced cofactor, oxidised reactant and/or reduced labelled reaction product according to the methods of the invention.
[0150] It will be apparent that as used herein, labelled organic molecules such as glucose, formate, and ethanol are not sources of .sup.xH.sup.+ ions.
[0151] Most preferably, the .sup.xH.sup.+ ions are provided as .sup.2H.sub.2O. The compositions of the invention can comprise unlabelled water (H.sub.2O) or can be free of H.sub.2O. Preferably, when the .sup.xH.sup.+ ions used in the methods of the invention are .sup.2H.sup.+ ions, the ratio of .sup.2H.sup.+ to H.sup.+ ions (i.e. H.sub.2O) is at least 1:99, such as at least 10:90, more preferably at least 20:80 e.g. at least 50:50 such as at least 80:20, more preferably at least 90:10 e.g. at least 95:5 such as at least 99:1. Preferably, when the .sup.xH.sup.+ ions used in the methods of the invention are .sup.2H.sup.+ ions, the composition comprising (i) H.sup.+ ions is free or essentially free of H.sub.2O (e.g. less than 0.1% or less than 0.01% H.sub.2O); i.e. when .sup.2H.sup.+ ions are used in the methods of the invention, the composition preferably comprises large amounts of .sup.2H.sup.+ ions.
[0152] In the methods of the invention, the concentration of .sup.xH.sup.+ ions in the composition comprising .sup.xH.sup.+ ions can be controlled to produce reduced labelled cofactor and/or labelled reaction product in the desired percentage purity. For example, for some applications it is desirable to produce reduced labelled cofactor or reduced labelled reaction product wherein the label is present at ppm levels, i.e. where the amount of reduced labelled cofactor or reduced labelled reaction product is from about 0.00001% to about 0.01%, such as from about 0.0001% to about 0.001%, relative to the amount of the unlabelled cofactor or product. In other applications it is desirable to produce reduced labelled cofactor or reduced labelled reaction product wherein the labelled cofactor or product is present in larger amounts, such as in amounts of from 1% to 100%, such as from 10% to about 99% e.g. from about 40% or about 50% to about 95% or about 90%, relative to the amount of the unlabelled cofactor or product. The extremely high efficiency of the reactions employed in the methods of the invention allow this to be controlled with accuracy by controlling the amount of .sup.xH.sup.+ ions in the composition comprising H.sup.+ ions. For example, if it is desired to produce reduced cofactor wherein 10% of the reduced cofactor is labelled with .sup.xH, this can be achieved by the use of a composition comprising 10% .sup.xH.sup.+ ions relative to the total number of H.sup.+ ions in the concentration.
[0153] For example, when it is desired to produce reduced labelled cofactor or reduced labelled reaction product wherein the label is present at ppm levels as described above, this can be achieved by use of a composition comprising .sup.xH.sup.+ ions in an amount of from about 0.00001% to about 0.01%, such as from about 0.0001% to about 0.001%, relative to the total amount of H.sup.+ ions in the concentration. Preferably, when 3H.sup.+ ions are used in the methods of the invention, the composition comprises ppm levels of 3H.sup.+ ions.
[0154] In the methods of the invention, any cofactor that can be reduced by an NADH:acceptor oxidoreductase or an NADPH:acceptor oxidoreductase or a functional derivative or fragment thereof as defined herein can be used. Preferably, the cofactor is nicotinamide adenine dinucleotide or nicotinamide adenine dinucleotide phosphate. More preferably, the cofactor is nicotinamide adenine dinucleotide.
[0155] Nicotinamide adenine dinucleotide exists in the oxidised form (NAD.sup.+) and the reduced form (NADH). Similarly, nicotinamide adenine dinucleotide phosphate exists in the oxidised form (NADP.sup.+) and the reduced form (NADPH). The oxidized forms NAD.sup.+ and NADP.sup.+ act as electron acceptors, by being reduced. NADH and NADPH, in turn, can act as reducing agents, by being oxidized. Those skilled in the art will appreciate that the term NAD(P)H refers to either NADH or NADPH. The term NAD(P).sup.+ refers to either NAD.sup.+ or NADP.sup.+. The structures of NAD.sup.+ and NADP.sup.+ are shown below:
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[0156] As described herein, the methods of the invention comprise reduction of an oxidised cofactor. Preferably, the reduction involves adding an .sup.xH atom at the 4-position of the nicotinamide ring of the oxidised cofactor, as shown below. (The 4-position of the nicotinamide ring in NAD.sup.+ and NADP.sup.+ is indicated above).
##STR00002##
[0157] The 4-position of the nicotinamide ring in NAD.sup.+ and NADP.sup.+ comprises a hydrogen atom. In NAD.sup.+ and NADP.sup.+, that hydrogen atom is typically .sup.1H. However, the methods of the invention are not limited to methods wherein the hydrogen atom at the 4-position of the nicotinamide ring is .sup.1H, but also embrace those methods wherein the hydrogen atom at the 4-position of the nicotinamide ring of the oxidised cofactor is .sup.2H or .sup.3H. In other words, in the methods of the invention, the oxidised cofactor is NAD.sup.+, NADP.sup.+, or a labelled version of NAD.sup.+ or NADP.sup.+ comprising at least one .sup.xH atom, typically wherein the .sup.xH atom is at the 4-position of the nicotinamide ring.
[0158] The methods of the invention can be used to generate both stereoisomers of the singularly labelled reduced cofactor, the doubly labelled reduced cofactor and the labelled oxidised cofactor; i.e. [4S-.sup.xH]-NAD(P)H, [4R-.sup.xH]-NAD(P)H, [4-.sup.xH.sub.2]-NAD(P)H and [4-.sup.xH]-NAD(P).sup.+. As used herein, the term [4S-.sup.xH]-NAD(P)H refers to the reduced form of NAD(P)H wherein the carbon atom at the 4-position of the nicotinamide ring is bonded to a .sup.1H atom and an .sup.xH atom and wherein the absolute stereochemistry at that carbon position is S, as defined by the Cahn-Ingold-Prelog rules. As used herein, the term [4R-.sup.xH]-NAD(P)H refers to the reduced form of NAD(P)H wherein the carbon atom at the 4-position of the nicotinamide ring is bonded to a .sup.1H atom and an .sup.xH atom and wherein the absolute stereochemistry at that carbon position is R, as defined by the Cahn-Ingold-Prelog rules. As used herein, the term [4-.sup.xH.sub.2]-NAD(P)H refers to the reduced form of NAD(P)H wherein the carbon atom at the 4-position of the nicotinamide ring is bonded to two .sup.xH atoms. As used herein, the term [4-.sup.xH]-NAD(P).sup.+ refers to the oxidised form of NAD(P)H wherein the carbon atom at the 4-position of the nicotinamide ring is bonded to one .sup.xH atom. Preferably, in the methods of the invention, the oxidised cofactor is NAD.sup.+ or NADP.sup.+. Most preferably, the oxidised cofactor is NAD.sup.+. Accordingly, the invention also provides methods for producing an oxidised labelled cofactor comprising an .sup.xH atom, wherein x is 2 or 3, comprising producing a reduced labelled cofactor comprising one or more .sup.xH atom according to the methods of the invention; and oxidising the reduced labelled cofactor thus produced.
[0159] The methods of the invention involve transferring electrons from an electron source to a first polypeptide which is an NADH:acceptor oxidoreductase or an NADPH:acceptor oxidoreductase or a functional derivative or fragment thereof, and contacting .sup.xH.sup.+ ions and oxidised cofactor with the first polypeptide thereby reducing the oxidised cofactor to form a reduced labelled cofactor comprising one or more .sup.xH atoms.
[0160] Those skilled in the art will appreciate that contacting .sup.xH.sup.+ ions and oxidised cofactor with the first polypeptide involves the direct contact of the .sup.xH.sup.+ ions with the first polypeptide and the direct transfer of said .sup.xH.sup.+ ions to the first polypeptide. In other words, the .sup.xH.sup.+ ions are transferred directly from the composition in which they are contained (e.g. directly from .sup.xH.sub.2O, e.g. directly from .sup.2H.sub.2O or .sup.3H.sub.2O) to the first polypeptide. The transfer of the .sup.xH.sup.+ ions to the first polypeptide is a consequence of the contacting of the .sup.xH.sup.+ ions with the first polypeptide. As explained above, labelled organic molecules such as glucose, formate, and ethanol are not sources of .sup.xH.sup.+ ions as used herein. As such, those skilled in the art will appreciate that .sup.xH.sup.+ ions are not transferred to the first polypeptide by contacting the first polypeptide by such labelled organic molecules.
[0161] Furthermore, the invention does not involve the abstraction of .sup.xH.sup.+ ions from such labelled organic molecules, irrespective of whether such labelled organic molecules are provided exogenously or generated in situ, e.g. by chemical exchange with .sup.xH.sub.2O. Thus, the methods of the invention do not involve the use of labelled organic molecules as co-substrates to mediate the transfer of .sup.xH.sup.+ ions from the composition in which they are contained (e.g. directly from .sup.xH.sub.2O, e.g. directly from .sup.2H.sub.2O or .sup.3H.sub.2O) to the first polypeptide.
[0162] Preferably, therefore, in the invention, contacting the .sup.xH.sup.+ ions and the oxidised cofactor with the first polypeptide comprises directly transferring an .sup.xH.sup.+ ion to the first polypeptide. Preferably, contacting the .sup.xH.sup.+ ions and the oxidised cofactor with the first polypeptide comprises directly transferring an .sup.xH.sup.+ ion directly from .sup.xH.sub.2O, e.g. directly from .sup.2H.sub.2O or .sup.3H.sub.2O) to the first polypeptide. Preferably, contacting the .sup.xH.sup.+ ions and the oxidised cofactor with the first polypeptide comprises directly transferring an .sup.xH.sup.+ ion directly from .sup.xH.sub.2O, e.g. directly from .sup.2H.sub.2O or .sup.3H.sub.2O) to the first polypeptide without transferring an .sup.xH.sup.+ ion to an organic molecule (i.e. to a co-substrate). Preferably, the methods of the invention do not comprise contacting the first polypeptide with a labelled organic reactant containing an .sup.xH atom. Preferably, the methods of the invention do not comprise transferring an .sup.xH.sup.+ ion from .sup.xH.sub.2O (e.g. from .sup.2H.sub.2O or .sup.3H.sub.2O) to an organic molecule (i.e. to a co-substrate). Preferably, the methods of the invention do not comprise transferring an .sup.xH.sup.+ ion from an organic molecule (i.e. a co-substrate) to the first polypeptide. In other words, the methods of the invention preferably do not comprise using a labelled organic molecule as a co-substrate to mediate the transfer of .sup.xH.sup.+ ions from the composition in which they are contained (e.g. from .sup.xH.sub.2O, e.g. from .sup.2H.sub.2O or .sup.3H.sub.2O) to the first polypeptide.
[0163] Accordingly, the invention preferably provides a method of producing a reduced labelled cofactor comprising one or more .sup.xH atom, wherein x is 2 or 3, wherein said method comprises:
[0164] i) providing a composition comprising (i) .sup.xH.sup.+ ions and (ii) an oxidised cofactor;
[0165] ii) transferring electrons from an electron source to a first polypeptide which is an NADH:acceptor oxidoreductase or an NADPH:acceptor oxidoreductase or a functional derivative or fragment thereof; and
[0166] iii) contacting the .sup.xH.sup.+ ions and the oxidised cofactor with the first polypeptide, thereby directly transferring an .sup.xH.sup.+ ion to the first polypeptide, and thereby reducing the oxidised cofactor to form a reduced labelled cofactor comprising one or more .sup.xH atoms. [0167] Preferably, said method is a method of producing a reduced labelled reaction product comprising one or more .sup.xH atom, wherein x is 2 or 3, and said method comprises producing a reduced labelled cofactor as defined herein; and
[0168] iv) contacting the reduced labelled cofactor and an oxidised reactant with at least one enzyme that is an NADH-dependent oxidoreductase or an NADPH-dependent oxidoreductase or a functional derivative or fragment thereof such that the enzyme selectively transfers an .sup.xH atom from the reduced labelled cofactor to the oxidised reactant thereby producing a reduced labelled reaction product and an oxidised cofactor. [0169] As described herein in more detail, such methods preferably further comprise reducing the oxidised cofactor produced in step (iv) in a method of the invention. Such methods may likewise comprise producing a reduced labelled reaction product according to steps (i) to (iv), and repeating steps (ii) to (iv) multiple times, thereby recycling the cofactor.
[0170] In the methods of the invention, any suitable NADH:acceptor oxidoreductase or NADPH:acceptor oxidoreductase or functional derivative or fragment thereof can be used as the first polypeptide. An NADH:acceptor oxidoreductase or NADPH:acceptor oxidoreductase or functional derivative or fragment thereof can be referred to as a diaphorase or diaphorase moiety.
[0171] As used herein, a NADH:acceptor oxidoreductase is a polypeptide capable of catalysing the reduction of NAD.sup.+ to NADH. As used herein, a NADPH:acceptor oxidoreductase is a polypeptide capable of catalysing the reduction of NADP.sup.+ to NADPH. It will be apparent to the skilled person that an NAD(P)H:acceptor oxidoreductase may either be a single polypeptide or may comprise multiple polypeptides, e.g. additional peptides in addition to the NAD(P)H:acceptor oxidoreductase. The NAD(P)H:acceptor oxidoreductase may also be a portion such as one or more domains of a multidomain polypeptide.
[0172] The first polypeptide preferably transfers an .sup.xH.sup. anion (wherein x=2 or 3) to the oxidised cofactor thereby forming the reduced labelled cofactor. Without being bound by theory, it is believed that the .sup.xH.sup. ion is transferred to the oxidised cofactor in a concerted two electron, one .sup.xH.sup.+ process, the two electrons and single proton combining to form an .sup.xH.sup. anion. The two electrons and single proton are believed to be typically transferred by a cofactor such as a flavin cofactor contained in the first polypeptide. However, as those skilled in the art will appreciate the precise mechanism by which the .sup.xH.sup. ion is transferred to the oxidised cofactor is immaterial to the efficacy of the overall process.
[0173] Preferably, the first polypeptide comprises a cofactor such as a flavin group. Preferably, the flavin group is an FAD (flavin adenine dinucleotide) or FMN (flavin mononucleotide) group.
[0174] Preferably, the structure of the first polypeptide is suitable for binding nucleotides such as NAD(P).sup.+ or NAD(P)H. A preferred structural motif for binding such nucleotides is the Rossmann fold. The Rossmann fold can be considered as a super-secondary structural motif characterized by alternating beta strand/alpha helix/beta strand secondary structures. Typically, Rossmann folds comprise up to four helices and a sheet typically comprising 6 strands. Proteins comprising Rossmann folds are well known to those skilled in the art.
[0175] Preferably, the first polypeptide comprises or consists of a diaphorase moiety. Diaphorases are a ubiquitous class of flavin-containing enzymes that typically catalyze the reduction of various dyes which act as hydrogen acceptors from NADH and NADPH. Diaphorases can be obtained from bacteria, plants and animals. Any suitable diaphorase capable of reducing an oxidised cofactor as defined herein in the presence of electrons and .sup.xH.sup.+ ions can be used in the methods of the invention.
[0176] Preferably, the first polypeptide comprises or consists of one or more than one of: [0177] i) the amino acid sequence of Ralstonia eutropha diaphorase HoxF (SEQ ID NO: 1) or an amino acid sequence having at least 60% homology therewith; [0178] ii) the amino acid sequence of Ralstonia eutropha diaphorase HoxU (SEQ ID NO: 2) or an amino acid sequence having at least 60% homology therewith; [0179] iii) the amino acid sequence of Ralstonia eutropha diaphorase HoxI (SEQ ID NO: 3) or an amino acid sequence having at least 60% homology therewith; [0180] iv) the amino acid sequence of the 51 kDa protein of the flavoprotein (Fp) subcomplex of Complex I of Bos taurus (SEQ ID NO: 4) or an amino acid sequence having at least 60% homology therewith; [0181] v) the amino acid sequence of the 24 kDa subcomplex of Complex I of Bos taurus (SEQ ID NO: 5) or an amino acid sequence having at least 60% homology therewith; [0182] vi) the amino acid sequence of Ralstonia eutropha NAD.sup.+-dependent formate dehydrogenase diaphorase moiety FdsB (SEQ ID NO: 6) or an amino acid sequence having at least 60% homology therewith; [0183] vii) the amino acid sequence of Ralstonia eutropha NAD.sup.+-dependent formate dehydrogenase diaphorase moiety FdsG (SEQ ID NO: 7) or an amino acid sequence having at least 60% homology therewith; [0184] viii) the amino acid sequence of Rhodobacter capsulatus NAD.sup.+-dependent formate dehydrogenase, diaphorase moiety FdsB (SEQ ID NO: 8) or an amino acid sequence having at least 60% homology therewith; [0185] ix) the amino acid sequence of Rhodobacter capsulatus NAD.sup.+-dependent formate dehydrogenase, diaphorase moiety FdsG (SEQ ID NO: 9) or an amino acid sequence having at least 60% homology therewith; [0186] x) the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase I gamma subunit (SEQ ID NO: 10) or an amino acid sequence having at least 60% homology therewith; [0187] xi) the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase I beta subunit (SEQ ID NO: 11) or an amino acid sequence having at least 60% homology therewith; [0188] xii) the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase II gamma subunit (SEQ ID NO: 12) or an amino acid sequence having at least 60% homology therewith; [0189] xiii) the amino acid sequence of the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase II beta subunit (SEQ ID NO: 13) or an amino acid sequence having at least 60% homology therewith; [0190] xiv) the amino acid sequence of the diaphorase moiety of Rhodococcus opacus soluble hydrogenase HoxF (SEQ ID NO: 14) or an amino acid sequence having at least 60% homology therewith; [0191] xv) the amino acid sequence of the diaphorase moiety of Rhodococcus opacus soluble hydrogenase HoxU (SEQ ID NO: 15) or an amino acid sequence having at least 60% homology therewith; [0192] xvi) the amino acid sequence of the diaphorase moiety of Allochromatium vinosum soluble hydrogenase HoxF (SEQ ID NO: 16) or an amino acid sequence having at least 60% homology therewith; [0193] xvii) the amino acid sequence of the diaphorase moiety of Allochromatium vinosum soluble hydrogenase HoxU (SEQ ID NO: 17) or an amino acid sequence having at least 60% homology therewith; [0194] xviii) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina Hox1F (SEQ ID NO: 18) or an amino acid sequence having at least 60% homology therewith; [0195] xix) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina soluble hydrogenase Hox1U (SEQ ID NO: 19) or an amino acid sequence having at least 60% homology therewith; [0196] xx) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina Hox2F (SEQ ID NO: 20) or an amino acid sequence having at least 60% homology therewith; [0197] xxi) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina soluble hydrogenase Hox2U (SEQ ID NO: 21) or an amino acid sequence having at least 60% homology therewith; [0198] xxii) the amino acid sequence of the diaphorase moiety of Synechocystis sp. PCC 6803 HoxF (SEQ ID NO: 22) or an amino acid sequence having at least 60% homology therewith; [0199] xxiii) the amino acid sequence of the diaphorase moiety of Synechocystis sp. PCC 6803 HoxU (SEQ ID NO: 23) or an amino acid sequence having at least 60% homology therewith; [0200] xxiv) the amino acid sequence of the diaphorase moiety of Synechococcus elongatus PCC 6301 HoxF (SEQ ID NO: 24) or an amino acid sequence having at least 60% homology therewith; [0201] xxv) the amino acid sequence of the diaphorase moiety of Synechococcus elongatus PCC 6301 HoxU (SEQ ID NO: 25) or an amino acid sequence having at least 60% homology therewith; [0202] xxvi) the amino acid sequence of Hydrogenophilus thermoluteolus diaphorase HoxF (SEQ ID NO: 26) or an amino acid sequence having at least 60% homology therewith; [0203] xxvii) the amino acid sequence of Hydrogenophilus thermoluteolus diaphorase HoxU (SEQ ID NO: 27) or an amino acid sequence having at least 60% homology therewith; [0204] xxviii) the amino acid sequence of Chlamydomonas reinhardtii Ferredoxin-NADP.sup.+ reductase (SEQ ID NO: 28) or an amino acid sequence having at least 60% homology therewith; [0205] xxix) the amino acid sequence of Anabaena Ferredoxin-NADP.sup.+ reductase (SEQ ID NO: 29) or an amino acid sequence having at least 60% homology therewith; [0206] xxx) the amino acid sequence of Ralstonia eutropha diaphorase HoxF (SEQ ID NO: 70) or an amino acid sequence having at least 60% homology therewith; [0207] xxxi) the amino acid sequence of Ralstonia eutropha diaphorase with inactive hydrogenase (SEQ ID NO: 1 and/or 2 and/or 69 and/or 31) or an amino acid sequence having at least 60% homology therewith [0208] or a functional fragment, derivative or variant thereof.
[0209] One or more of the amino acid sequences described in (i) to (xxxi) above can be used as the first polypeptide.
[0210] When the first polypeptide comprises a variant of SEQ ID NO: 1, the variant may comprise point mutations such that the variant comprises one or more of the following mutations: [0211] i) K, S, A, N, R or H at position 326; more preferably, the variant comprises D326K; [0212] ii) K, S, A, N, R or H at position 401; more preferably, the variant comprises D401K; [0213] iii) K, S, A, N, R or H at position 467; more preferably, the variant comprises D467S; [0214] iv) K, S, A, N, R or H at position 340; more preferably, the variant comprises D340A; and/or [0215] v) K, S, A, N, R or H at position 341; more preferably, the variant comprises E341A or H341.
[0216] The above mutations are complementary and can be combined, for example, when the first polypeptide is a variant of SEQ ID NO: 1, the variant may preferably comprises D340A and E341A; D340A and D401K; D326K and D401K; D467S and D401K; D340N and D467S; and/or E341A and D467S. Without being bound by theory, it is believed that such variants can accommodate the additional negatively charged phosphate group of NADP.sup.+ resulting in improved affinity and/or oxidation and/or reduction activity due to reduced negative charge around the NADP.sup.+ binding site.
[0217] The first polypeptide preferably comprises or consists of the amino acid sequence of Ralstonia eutropha soluble hydrogenase moiety HoxF (SEQ ID NO: 1) or an amino acid sequence having at least 60% homology therewith. The first polypeptide can optionally further comprise the amino acid sequence of Ralstonia eutropha soluble hydrogenase moiety HoxU (SEQ ID NO: 2) or an amino acid sequence having at least 60% homology therewith. Accordingly, the first polypeptide may comprise or consist of the amino acid sequence of Ralstonia eutropha soluble hydrogenase moieties HoxFU (SEQ ID NOs: 1, 2) or amino acid sequences having at least 60% homology therewith.
[0218] When the first polypeptide comprises the amino acid sequence of Ralstonia eutropha soluble hydrogenase moiety HoxF (SEQ ID NO: 1) or an amino acid sequence having at least 60% homology therewith, and optionally the amino acid sequence of Ralstonia eutropha soluble hydrogenase moiety HoxU (SEQ ID NO: 2) or an amino acid sequence having at least 60% homology therewith, the first polypeptide may optionally further comprise the amino acid sequence of Ralstonia eutropha soluble hydrogenase moieties HoxH and/or HoxY (SEQ ID NOs: 30, 31) or amino acid sequences having at least 60% homology therewith. Without being bound by theory, it is believed that the presence of a HoxHY component in the first polypeptide increases the stability of the NADH:acceptor oxidoreductase or NADPH:acceptor oxidoreductase moiety leading to increased efficiency and/or activity. Many suitable methods for increasing the stability of proteins/protein complexes are known in the art and may be used in the methods of the present invention.
[0219] Preferably, therefore, the first polypeptide comprises a HoxHYFU tetramer. More preferably, the first polypeptide comprises the HoxHYFU tetramer of Ralstonia eutropha (SEQ ID NOs: 1, 2, 30, 31), or an amino acid sequence having at least 60% homology therewith. Still more preferably, the first polypeptide comprises the HoxHYFU tetramer of Ralstonia eutropha wherein the HoxH moiety is a non-functional variant, preferably comprising the point mutation I64A (SEQ ID NO: 69), or a sequence having at least 60% homology therewith (in which case the HoxH moiety comprises the point mutation I64A). HoxHYFU constructs comprising the I64A point mutation in the HoxH moiety are also known as HoxFU or NAD-R (SEQ ID NOs: 1, 2, 31, 69).
[0220] Preferably, when the first polypeptide comprises or consists of one or more amino acid sequences having at least 60% homology with a specified sequence, each amino acid sequence independently has at least 70%, such as at least 80%, more preferably at least 90%, e.g. at least 95%, preferably at least 97%, such as at least 98%, preferably at least 99% homology with the specified sequence. More preferably, each amino acid sequence independently has at least 70%, such as at least 80%, more preferably at least 90%, e.g. at least 95%, preferably at least 97%, such as at least 98%, preferably at least 99% identity with the specified sequence. For avoidance of doubt, if the first polypeptide comprises two or more amino acid sequences, the percentage homology of each of the two or more sequences with respect to their respective specified sequences can be the same or different. Percentage homology and/or percentage identity are each preferably determined across the length of the specified sequence.
[0221] Variants of NADH:acceptor oxidoreductase or NADPH:acceptor oxidoreductases are also suitable for use as the first polypeptide in the methods of the present invention. For example, the first polypeptide may preferably be modified to have an increased catalytic activity for reducing the oxidised cofactor or oxidising the reduced cofactor as compared to the native enzymes. Preferably, variants have increased catalytic activity as compared to the activity of the Ralstonia eutropha diaphorase HoxF or HoxFU moieties (SEQ ID NOs 1, 2). Preferably, the catalytic activity is at least 2 times, such as at least 5 times, e.g. at least 10 times, such as at least 100 times, preferably at least 1000 times the catalytic activity of the Ralstonia eutropha diaphorase HoxF or HoxFU moieties.
[0222] Catalytic activity can be determined in any suitable method. For example, the catalytic activity can be associated with the Michaelis constant K.sub.M (with increased activity being typically associated with decreased K.sub.M values) or with the catalytic rate constant, k.sub.cat (with increased activity being typically associated with increased k.sub.cat values). Measuring K.sub.M and k.sub.cat is routine to those skilled in the art. For example, the K.sub.M of the first polypeptide for a reduced cofactor can be determined spectrophotometrically by measuring absorption at 578 nm under anaerobic conditions at 30 C. in 50 mM Tris-HCl buffer, pH 8.0, containing 1 mM reduced cofactor, 5 mM benzyl viologen (oxidized; e=8.9 mM.sup.1 cm.sup.1), 90 M dithionite, and 10 to 30 pmol of enzyme. Alternatively, the K.sub.M of the first polypeptide for oxidised cofactor can be determined electrochemically, by adsorbing the first polypeptide onto a pyrolytic graphite electrode immersed in an electrochemical cell containing buffered electrolyte (eg 50 mM phosphate at pH 7.0) and holding the electrode at a constant potential of 412 mV vs a standard hydrogen electrode while the concentration of the oxidised cofactor is increased by injection into the solution. The intercept on the (substrate concentration) axis of a plot of (substrate concentration)/(current magnitude) vs (substrate concentration) is equal to (K.sub.M) (Lauterbach et al, PLoS ONE; doi:10.1371/journal.pone.0025939). The intercept on the (substrate concentration)/(current magnitude) axis of such a plot is equal to K.sub.M/V.sub.max with V.sub.max=k.sub.cat[E] where [E] is the amount of enzyme present, which can typically be determined by integrating the background-subtracted redox peak observed for the enzyme in the absence of substrate.
[0223] More preferably, the first polypeptide consists or comprises of the Ralstonia eutropha NAD.sup.+-reducing soluble hydrogenase or a functional fragment, derivative or variant thereof. Still more preferably, the first polypeptide consists or comprises of the R. eutropha HoxF moiety (SEQ ID NO: 1) and optionally the HoxU diaphorase moieties (SEQ ID NO: 2) or an amino acid sequence having at least 60% homology (e.g. at least 70%, such as at least 80%, more preferably at least 90%, e.g. at least 95%, preferably at least 97%, such as at least 98%, preferably at least 99% homology) therewith. More preferably the first polypeptide consists or comprises of the HoxHYFU tetramer of Ralstonia eutropha (SEQ ID NOs: 1, 2, 30, 31), or an amino acid sequence having at least 60% homology (e.g. at least 70%, such as at least 80%, more preferably at least 90%, e.g. at least 95%, preferably at least 97%, such as at least 98%, preferably at least 99% homology) therewith. Most preferably, the first polypeptide comprises HoxFU(also referred to herein as NAD-R, i.e. the HoxHYFU tetramer of Ralstonia eutropha wherein the HoxH moiety comprises the point mutation I64A (SEQ ID NOs: 1, 2, 31, 69)), or a sequence having at least 60% homology (e.g. at least 70%, such as at least 80%, more preferably at least 90%, e.g. at least 95%, preferably at least 97%, such as at least 98%, preferably at least 99% homology) therewith (wherein the HoxH moiety comprises the point mutation I64A).
[0224] In the methods of the invention, the electron source preferably comprises a second polypeptide capable of oxidising a reductant to extract electrons (as illustrated in
[0225] Preferably, the reductant is an organic compound such as formate, glucose, an alcohol, or the like, or is hydrogen (i.e. H.sub.2 or .sup.xH.sub.2 or mixtures thereof). Where the reductant is other than hydrogen, preferably the reductant is unlabelled. In one embodiment, the reductant is unlabelled. More preferably, the reductant is selected from formate, glucose, ethanol, H.sub.2, .sup.xH.sub.2 or mixtures thereof. Still more preferably, the reductant is H.sub.2 or .sup.xH.sub.2 or mixtures thereof. Those skilled in the art can readily determine the most suitable reductant for a given application. For example, when high purity of the labelled cofactor or reduced reaction product is prioritised, the reductant is often preferably .sup.xH.sub.2. When reduced costs or high throughput is prioritised, the reductant is often preferably H.sub.2. Most usually it is preferred that the reductant is H.sub.2.
[0226] When the reductant is H.sub.2 or .sup.xH.sub.2, the second polypeptide and/or the synthetic organic, inorganic or metallic oxidation catalyst is preferably selected or modified to catalyze H.sub.2 or .sup.xH.sub.2 oxidation close to the thermodynamic potential E.sup.o of the 2H.sup.+/H.sub.2 couple
[0227] (E.sup.o(2H.sup.+/H.sub.2)) under the experimental conditions. (Those skilled in the art will appreciate that E.sup.o (2H.sup.+/H.sub.2)=0.413 V at 25 C., pH 7.0 and 1 bar H.sub.2, and varies according to the Nernst equation). Preferably, the second polypeptide and/or the synthetic organic, inorganic or metallic oxidation catalyst is preferably selected or modified to catalyze H.sub.2 or .sup.xH.sub.2 oxidation at applied potentials of less than 100 mV more positive than E.sup.o (2H.sup.+/H.sub.2); more preferably at applied potentials of less than 50 mV more positive than E.sup.o (2H.sup.+/H.sub.2). Methods of determining the ability of a catalyst such as a second polypeptide or a synthetic organic, inorganic or metallic oxidation catalyst as defined herein to catalyze H.sub.2 or .sup.xH.sub.2 oxidation close to E.sup.o (2H.sup.+/H.sub.2) under the experimental conditions at issue are routine for those skilled in the art and are, for example, described in Vincent et al, J. Am. Chem. Soc. (2005) 127, 18179-18189.
[0228] When the electron source comprises a second polypeptide, the second polypeptide is preferably an oxidising enzyme or functional derivative or fragment thereof capable of oxidising a reductant to extract electrons, wherein the second polypeptide transfers electrons from the reductant to the first polypeptide via an electronically-conducting pathway. Those skilled in the art will appreciate that as used herein, an oxidising enzyme is an enzyme capable of oxidising a reductant to extract electrons and deliver those electrons to a suitable electronically-conducting pathway for transfer to the first polypeptide. As used herein, the term oxidising enzyme thus also includes enzymes such as oxidases and dehydrogenases.
[0229] When the electron source comprises a second polypeptide, the first polypeptide and the second polypeptide may constitute component parts of a modular, multidomain or multicomponent protein or protein complex. This is shown schematically in
[0230] When the first polypeptide and the second polypeptide constitute component parts of a modular, multidomain or multicomponent protein or protein complex, the first and second polypeptide are preferably either native partners or genetically fused redox partners. More preferably, the first and second polypeptide are native partners. As those skilled in the art will appreciate, native partners are associated together in vivo and are typically attached via non-covalent means such as by non-specific interactions, hydrophobic interactions, hydrophilic interactions (including hydrogen bonds), ionic interactions, and Van der Waals forces. In some embodiments, however, when the electron source comprises a second polypeptide, the first polypeptide and the second polypeptide are not native partners; i.e. they do not occur together in nature as an enzyme complex and in the cellular environment electrons are not transferred from the second polypeptide to the first polypeptide. In such embodiments, it is preferable that the first polypeptide and the second polypeptide are selected from or derived from different bacterial species or from different bacterial genera, or the first polypeptide and the second polypeptide are selected from or derived from the same bacterial genus or species, but from different enzymes within the said same bacterial genus or species.
[0231] When the first polypeptide and the second polypeptide constitute component parts of a modular, multidomain or multicomponent protein or protein complex, the electron-conducting pathway from the first polypeptide to the second polypeptide can comprise any suitable means. Preferably, the electron transfer pathway comprises metal centres such as metal atoms (e.g. in heme centres) or metal clusters, preferably iron-sulphur-containing clusters [FeS]-clusters. As those skilled in the art will appreciate, [FeS]-clusters include [3Fe4S] and [4Fe4S] clusters.
[0232] Preferably, when the electron source comprises a second polypeptide, the second polypeptide is selected or modified to oxidise H.sub.2 or .sup.xH.sub.2 (wherein x=2 or 3) under the conditions of the method. More preferably the second polypeptide is a hydrogenase enzyme or a functional derivative or fragment thereof. Any suitable hydrogenase can be used. Preferably, the hydrogenase comprises an active site comprising iron atoms (as in the [FeFe]-hydrogenases) or both nickel and iron atoms (as in the [NiFe]- and [NiFeSe]-hydrogenases).
[0233] Preferably, when the electron source comprises a second polypeptide which is a hydrogenase, the hydrogenase is selected or modified to be oxygen tolerant. Oxygen tolerant hydrogenases are capable of oxidising H.sub.2 or .sup.xH.sub.2 in the presence of oxygen, such as in the presence of at least 0.01% O.sub.2, preferably at least 0.1% O.sub.2, more preferably at least 1% O.sub.2, such as at least 5% O.sub.2, e.g. at least 10% O.sub.2 such as at least 20% O.sub.2 or more whilst retaining at least 1%, preferably at least 5%, such as at least 10%, preferably at least 20%, more preferably at least 50% such as at least 80% e.g. at least 90% preferably at least 95% e.g. at least 99% of their H.sub.2 or .sup.xH.sub.2-oxidation activity under anaerobic conditions. Various oxygen-tolerant hydrogenases are known to those skilled in the art.
[0234] Preferably, when the electron source comprises a second polypeptide which is a hydrogenase, the hydrogenase comprises or consists of: [0235] i) the amino acid sequence of Ralstonia eutropha soluble hydrogenase moiety (SEQ ID NOs: 30 and/or 31) or an amino acid sequence having at least 60% homology therewith; [0236] ii) the amino acid sequence of Ralstonia eutropha membrane-bound hydrogenase moiety (SEQ ID NOs: 32 and/or 33 and/or 34) or an amino acid sequence having at least 60% homology therewith; [0237] iii) the amino acid sequence of Ralstonia eutropha regulatory hydrogenase moiety (SEQ ID NOs: 35 and/or 36) or an amino acid sequence having at least 60% homology therewith; [0238] iv) the amino acid sequence of Escherichia coli hydrogenase 1 (SEQ ID NOs:37 and/or 38) or an amino acid sequence having at least 60% homology therewith; [0239] v) the amino acid sequence of Escherichia coli hydrogenase 2 (SEQ ID NOs:39 and/or 40) or an amino acid sequence having at least 60% homology therewith; [0240] vi) the amino acid sequence of Aquifex aeolicus hydrogenase 1 (SEQ ID NO:41 and/or 42) or an amino acid sequence having at least 60% homology therewith; [0241] vii) the amino acid sequence of Hydrogenovibrio marinus hydrogenase (SEQ ID NOs: 43 and/or 44) or an amino acid sequence having at least 60% homology therewith; [0242] viii) the amino acid sequence of Thiocapsa roseopersicina hydrogenase (SEQ ID NOs: 45 and 46) or an amino acid sequence having at least 60% homology therewith; [0243] ix) the amino acid sequence of Alteromonas macleodii hydrogenase (SEQ ID NOs: 47 and/or 48) or an amino acid sequence having at least 60% homology therewith; [0244] x) the amino acid sequence of Rhodococcus opacus soluble hydrogenase moiety (SEQ ID NOs: 49 and/or 50) or an amino acid sequence having at least 60% homology therewith; [0245] xi) the amino acid sequence of Allochromatium vinosum membrane bound hydrogenase (SEQ ID NOs: 51 and/or 52) or an amino acid sequence having at least 60% homology therewith; [0246] xii) the amino acid sequence of Desulfovibrio fructosovorans membrane bound hydrogenase (SEQ ID NOs: 53 and/or 54) or an amino acid sequence having at least 60% homology therewith; [0247] xiii) the amino acid sequence of Clostridium pasteurianum iron-iron hydrogenase (SEQ ID NOs: 55) or an amino acid sequence having at least 60% homology therewith; [0248] xiv) the amino acid sequence of Clostridium acetobutylicum iron-iron hydrogenase (SEQ ID NOs: 56) or an amino acid sequence having at least 60% homology therewith; [0249] xv) the amino acid sequence of Chlamydomonas reinhardtii iron-iron hydrogenase (SEQ ID NOs: 57) or an amino acid sequence having at least 60% homology therewith; [0250] xvi) the amino acid sequence of Desulfomicrobium baculatum nickel-iron selenium hydrogenase (SEQ ID NOs: 58 and/or 59) or an amino acid sequence having at least 60% homology therewith; [0251] xvii) the amino acid sequence of Hydrogenophilus thermoluteolus soluble hydrogenase moiety (SEQ ID NOs: 60 and/or 61) or an amino acid sequence having at least 60% homology therewith; [0252] xviii) the amino acid sequence of Desulfovibrio vulgaris Nickel Iron hydrogenase (pdb 1H2A) (SEQ ID NOs: 62 and/or 63) or an amino acid sequence having at least 60% homology therewith; [0253] xix) the amino acid sequence of Desulfovibrio gigas Periplasmic [NiFe] hydrogenase (SEQ ID NOs: 64 and/or 65) or an amino acid sequence having at least 60% homology therewith; [0254] xx) the amino acid sequence of Salmonella enterica serovar Typhimurium LT2 nickel-iron hydrogenase 5 (SEQ ID NO: 66 and/or 67) or an amino acid sequence having at least 60% homology therewith. [0255] xxi) the amino acid sequence of Pyrococcus furiosus soluble alpha subunit (SEQ ID NOs: 68) or an amino acid sequence having at least 60% homology therewith; [0256] or a functional fragment, derivative or variant thereof.
[0257] When the electron source comprises a second polypeptide which is a hydrogenase, the hydrogenase may optionally not comprise a FMN and/or a FAD prosthetic group. Without being bound by theory, it is believed that hydrogenases lacking such groups typically have increased stability compared to hydrogenases comprising such prosthetic groups. Examples of hydrogenases lacking a FMN prosthetic group include Ralstonia eutropha membrane-bound hydrogenase (SEQ ID NOs: 32-34), Ralstonia eutropha regulatory hydrogenase (SEQ ID NOs:35-36), Escherichia coli hydrogenase 1 (SEQ ID NOs:37-38), Escherichia coli hydrogenase 2 (SEQ ID NOs:39-40), Aquifex aeolicus hydrogenase 1 (SEQ ID NOs:41-42), Hydrogenovibrio marinus membrane-bound hydrogenase (SEQ ID NOs: 43-44), Desulfovibrio vulgaris Nickel Iron hydrogenase (SEQ ID NOs: 62-63) and Desulfovibrio gigas Periplasmic [NiFe] hydrogenase (SEQ ID NOs: 64-65). Such hydrogenases are particularly suitable when the first polypeptide and the second polypeptide constitute component parts of a modular, multidomain or multicomponent protein or protein complex.
[0258] Preferably, when the electron source comprises a second polypeptide which is a hydrogenase, the hydrogenase is selected from Escherichia coli hydrogenase 1 (SEQ ID NOs:37, 38), Escherichia coli hydrogenase 2 (SEQ ID NOs:39, 40), Ralstonia eutropha soluble hydrogenase (HoxHY, SEQ ID NOs: 30, 31), Hydrogenophilus thermoluteolus hydrogenase (SEQ ID NOs: 60, 61), Desulfovibrio gigas hydrogenase (SEQ ID NO: 64, 65), Desulfovibrio fructosovorans hydrogenase (SEQ ID NO: 53, 54) and Desulfovibrio vulgaris (SEQ ID NO: 62, 63), or an amino acid sequence having at least 60% homology therewith. Most preferably, the second polypeptide is Escherichia coli hydrogenase 1 (SEQ ID NOs: 37, 38), Escherichia coli hydrogenase 2 (SEQ ID NOs: 39, 40) or Ralstonia eutropha soluble hydrogenase (HoxHY, SEQ ID NOs: 30, 31).
[0259] In other circumstances where it is preferable that the reductant is not H.sub.2 or .sup.xH.sub.2, the second polypeptide may be preferably selected or modified to oxidise formate, glucose or an alcohol under the conditions of the method. When the reductant is glucose, the second polypeptide is preferably a glucose oxidase enzyme such as glucose dehydrogenase from Acinetobacter calcoaceticus (SEQ ID NO: 76), or Myriococcum thermophilum cellobiose dehydrogenase (SEQ ID NO: 75), or cellobiose dehydrogenase from Phanerochaete chrysosporium (SEQ ID NO: 73 and/or 74)) or an amino acid sequence having at least 60% homology therewith. When the reductant is an alcohol such as ethanol, the second polypeptide is preferably an alcohol dehydrogenase enzyme such as the PQQ- and heme-dependent ethanol dehydrogenase from Comamonas testosteroni (SEQ ID NO: 72). When the reductant is formate, the second polypeptide is preferably a formate dehydrogenase enzyme, more preferably the molybdenum-containing formate dehydrogenase H from Escherichia coli (EcFDH-H) (SEQ ID NO: 71), or an amino acid sequence having at least 60% homology therewith; or the tungsten-containing formate dehydrogenase 1 from Desulfovibrio gigas (SEQ ID NO: 77 and/or 78) or an amino acid sequence having at least 60% homology therewith. Most preferably, when the reductant is formate, the second polypeptide is the molybdenum-containing formate dehydrogenase H from Escherichia coli (EcFDH-H) (SEQ ID NO: 71).
[0260] Preferably, when the second polypeptide comprises or consists of one or more amino acid sequences having at least 60% homology with a specified sequence, each amino acid sequence independently has at least 70%, such as at least 80%, more preferably at least 90%, e.g. at least 95%, preferably at least 97%, such as at least 98%, preferably at least 99% homology with the specified sequence. More preferably, each amino acid sequence independently has at least 70%, such as at least 80%, more preferably at least 90%, e.g. at least 95%, preferably at least 97%, such as at least 98%, preferably at least 99% identity with the specified sequence. For avoidance of doubt, if the second polypeptide comprises two or more amino acid sequences, the percentage homology of each of the two or more sequences with respect to their respective specified sequences can be the same or different. Percentage homology and/or percentage identity are each preferably determined across the length of the specified reference sequence.
[0261] As described herein the first polypeptide and/or the second polypeptide (if present) may be a functional fragment, derivative or variant of an enzyme or amino acid sequence. As those skilled in the art will appreciate, fragments of amino acid sequences include deletion variants of such sequences wherein one or more, such as at least 1, 2, 5, 10, 20, 50 or 100 amino acids are deleted. Deletion may occur at the C-terminus or N-terminus of the native sequence or within the native sequence. Typically, deletion of one or more amino acids does not influence the residues immediately surrounding the active site of an enzyme. Derivatives of amino acid sequences include post-translationally modified sequences including sequences which are modified in vivo or ex vivo. Many different protein modifications are known to those skilled in the art and include modifications to introduce new functionalities to amino acid residues, modifications to protect reactive amino acid residues or modifications to couple amino acid residues to chemical moieties such as reactive functional groups on linkers or substrates (surfaces) for attachment to such amino acid residues.
[0262] Derivatives of amino acid sequences include addition variants of such sequences wherein one or more, such as at least 1, 2, 5, 10, 20, 50 or 100 amino acids are added or introduced into the native sequence. Addition may occur at the C-terminus or N-terminus of the native sequence or within the native sequence. Typically, addition of one or more amino acids does not influence the residues immediately surrounding the active site of an enzyme.
[0263] Variants of amino acid sequences include sequences wherein one or more amino acid such as at least 1, 2, 5, 10, 20, 50 or 100 amino acid residues in the native sequence are exchanged for one or more non-native residues. Such variants can thus comprise point mutations or can be more profound e.g. native chemical ligation can be used to splice non-native amino acid sequences into partial native sequences to produce variants of native enzymes. Variants of amino acid sequences include sequences carrying naturally occurring amino acids and/or unnatural amino acids. Variants, derivatives and functional fragments of the aforementioned amino acid sequences retain at least some of the activity/functionality of the native/wild-type sequence. Preferably, variants, derivatives and functional fragments of the aforementioned sequences have increased/improved activity/functionality when compared to the native/wild-type sequence.
[0264] When the electron source comprises a synthetic (i.e. non-biological) organic, inorganic or metallic oxidation catalyst, the catalyst is any synthetic organic, inorganic or metallic oxidation catalyst capable of oxidising a reductant to extract electrons. As used herein, a synthetic oxidation catalyst includes substances such as metals which occur naturally but which are non-biological. As used herein, enzymes are not synthetic catalysts. As explained below, exemplary synthetic catalysts include metals and metal-containing compounds such as metal oxides, metal hydroxides, and the like.
[0265] The synthetic (non-biological) catalyst oxidises the reductant to form an oxidised product. The electrons extracted from the reductant are transferred via an electron conducting pathway to the first polypeptide. The electrons are used by the first polypeptide to reduce the oxidised cofactor as described herein.
[0266] Preferably, when the electron source comprises a synthetic oxidation catalyst, the synthetic oxidation catalyst is selected or modified to oxidise H.sub.2 or .sup.xH.sub.2 under the conditions of the method. Any suitable synthetic oxidation catalyst may be used. Many suitable H.sub.2/.sup.xH.sub.2 oxidation catalysts are known to those skilled in the art and can be readily applied in the methods of the invention.
[0267] Preferably, when the electron source comprises a synthetic oxidation catalyst, the synthetic oxidation catalyst is capable of oxidising H.sub.2 or .sup.xH.sub.2 in the presence of oxygen, such as in the presence of at least 0.01% O.sub.2, preferably at least 0.1% O.sub.2, more preferably at least 1% O.sub.2, such as at least 5% O.sub.2, e.g. at least 10% O.sub.2 such as at least 20% O.sub.2 or more whilst retaining at least 1%, preferably at least 5%, such as at least 10%, preferably at least 20%, more preferably at least 50% such as at least 80% e.g. at least 90% preferably at least 95% e.g. at least 99% of its H.sub.2 or .sup.xH.sub.2-oxidation activity under anaerobic conditions.
[0268] Preferably, the oxidation catalyst is a metal or metal-containing catalyst. Preferably, the oxidation catalyst comprises platinum, palladium, iridium, nickel, rhodium and/or ruthenium. More preferably, the oxidation catalyst comprises platinum. Many suitable metallic oxidation catalysts are known to those skilled in the art and can be readily applied in the methods of the invention. When the electron source comprises a non-metallic synthetic catalyst, any suitable non-metallic synthetic oxidation catalyst may be used. Preferable non-metallic synthetic oxidation catalysts include frustrated Lewis pair catalysts. Many such catalysts are known to those skilled in the art and can be readily applied in the methods of the invention.
[0269] In the methods of the invention, the electron source and the first polypeptide are preferably each in electronic contact with an electronically conducting support. More preferably, the electron source and the first polypeptide are each in electronic contact with the same electronically conducting support such that electrons flow from the electron source via the electronically conducting support to the first polypeptide.
[0270] Alternatively, the electron source may be in electronic contact with an electronically conducting first support and the first polypeptide in electronic contact with an electronically conducting second support; and the first support in electronic contact with the second support, such that electrons flow from the electron source to the electronically conducting first support, from the electronically conducting first support to the electronically conducting second support via the electronic contact between the first and second supports, and from the electronically conducting second support to the first polypeptide.
[0271] When the electron source and/or the first polypeptide are in electronic contact with a support, any suitable means of contact can be used. Preferably, the electron source and/or the first polypeptide are immobilized on the respective support(s). Any suitable means of contact can be used providing the electron source and/or the first polypeptide are immobilized in electronic contact with the support. As used herein, the term immobilized embraces adsorption, entrapment and/or cross-linkage between the support and the electron source or polypeptide. Adsorption embraces non-covalent interactions including electrostatic interactions, hydrophobic interactions, and the like. A charged adsorption enhancer such as polymyxin B sulphate can be used to enhance adsorption. Entrapment embraces containment of the electron source and/or the first polypeptide onto the surface of the support, e.g. within a polymeric film or in a hydrogel. Cross-linkage embraces covalent attachment, either directly between the electron source and/or the first polypeptide (e.g. via amide coupling, such as via EDC/NHS and/or other coupling agents routine to those skilled in the art) or using one or more covalent cross-linkers such as thiol-terminated linkers or crosslinking reagents. Immobilization means comprising or consisting of adsorption are preferred. Combination of some or all of the above mentioned immobilization means may be used.
[0272] Preferably, the or each support independently comprises a material comprising carbon, a metal or metal alloy, a metal oxide (include mixed metal oxides), a metal hydroxide (including layered double hydroxides), a metal chalcogenide, a semi-conducting material (including silicates, germanium compounds and gallium compounds such as silicon carbide, doped silicon and/or doped germanium) or an electronically-conductive polymer; or mixtures thereof. As those skilled in the art will appreciated, suitable support materials can include mixtures of materials described herein, such as mixtures of metal oxides or mixed metal oxides. Any suitable support material can be used.
[0273] More preferably, the or each support material independently comprises: [0274] i) carbon; and/or [0275] ii) a metal or metal alloy selected from gold, silver, tungsten, iridium, platinum, palladium, copper, titanium, brass, and steel; and/or [0276] iii) a material selected from titanium oxide, indium oxide, tin oxide and indium tin oxide.
[0277] Still more preferably, the or each support material comprises a carbon material. Still more preferably, the or each support material independently comprises a carbon material comprising graphite, carbon nanotube(s), carbon black, activated carbon, carbon nanopowder, vitreous carbon, carbon fibre(s), carbon cloth, carbon felt, carbon paper, graphene, highly oriented pyrolytic graphite, pyrolytic graphite, or doped diamond. Most preferably, the or each support material independently comprises a carbon material comprising graphite (or highly oriented pyrolytic graphite or pyrolytic graphite) or carbon black; most preferably carbon black.
[0278] Preferably, the or each support is an electronically conducting particle. Preferred electronically conducting particles comprise materials described herein. Preferably, when the or each support comprise particles, the particles have a particle size of from about 1 nm to about 100 m, such as from about 10 nm to about 10 m e.g. from about 100 nm to about 1 m. Methods of determining particle size are routine in the art and include, for example, dynamic light scattering. Suitable electronically conducting particles for use in the methods of the invention include conductive carbon black particles such as Black Pearls 2000 particles available from Cabot corp (Boston, Mass., USA).
[0279] When the electron source comprises an electrode connected to an electrode controller, any suitable electrode material can be used. Preferred electrode materials comprise carbon, a metal or metal alloy, a metal oxide (include mixed metal oxides), a metal hydroxide (including layered double hydroxides), a metal chalcogenide, or an electronically-conductive polymer; or mixtures thereof. Suitable electrode materials can include mixtures of materials described herein, such as mixtures of metal oxides or mixed metal oxides.
[0280] Preferred electrode materials comprise: [0281] i) carbon; and/or [0282] ii) a metal or metal alloy selected from gold, silver, tungsten, iridium, platinum, palladium, copper, titanium, brass, and steel; and/or [0283] iii) a material selected from titanium oxide, indium oxide, tin oxide and indium tin oxide.
[0284] More preferred electrode materials comprise a carbon material. Still more preferred electrode materials comprise a carbon material comprising graphite, carbon nanotube(s), carbon black, activated carbon, carbon nanopowder, vitreous carbon, carbon fibre(s), carbon cloth, carbon felt, carbon paper, graphene, highly oriented pyrolytic graphite, pyrolytic graphite, or doped diamond (e.g. boron-doped diamond). Most preferred electrode materials comprises carbon materials comprising graphite (or highly oriented pyrolytic graphite or pyrolytic graphite).
[0285] Preferably, in the methods of the invention, the first polypeptide and/or the electron source are provided in a form which can be easily removed from the reaction mixture. Preferably, the first polypeptide and the electron source comprise a heterogeneous system with the composition comprising .sup.xH.sup.+ ions. For example, the composition comprising .sup.xH.sup.+ ions is preferably a liquid and the first polypeptide and the electron source are in electronic contact with one or more electronically conducting support(s) which can be removed from the composition by sedimentation, filtration, centrifugation, or the like. For example, the first polypeptide and the electron source may be immobilized onto carbon materials as defined herein (e.g. carbon powder, carbon nanotubes, carbon black, carbon felt, activated carbon, or the like), and the carbon material(s) can be removed from the composition by sedimentation, filtration, centrifugation, etc. Many such methods are known to those skilled in the art, e.g. filtration can be achieved using a simple filter paper to remove solid components from a liquid composition; or a mixed solid/liquid composition can be allowed to settle and the liquid then decanted from the settled solids.
[0286] In the methods of the invention, electrons are transferred from the electron source to the first polypeptide. Preferably, electrons are directly transferred from the electron source to the first polypeptide along an electronically conducting pathway. Alternatively, electron transfer along the electronically-conducting pathway can be mediated by one or more electron mediators, as shown schematically in
[0287] In the methods of the invention, an electronically conducting pathway can be formed e.g. when the first polypeptide and the electron source are localised on the same electronically conducting supports. In another embodiment, the first polypeptide and the electron source can be localised or comprise or consist of different electronically conducting supports. In such cases the electronically-conducting pathway may comprise a linker such as a wire between the supports. The linker may be a molecular linker such as conductive polymeric strand or may be a metallic linker such as a metallic wire.
[0288] In the methods of the invention, the cofactor is preferably initially added to or present in an aqueous solution at a concentration of 1 M to 1 M, such as from 5 M to 800 mM, e.g. from 10 M to 600 mM such as from 25 M to 400 mM e.g. from 50 M to 200 mM such as from 100 M to about 100 mM e.g. from about 250 M to about 10 mM such as from about 500 M to about 1 mM.
[0289] The methods of the invention are typically conducted under a gas atmosphere; i.e. in the presence of gas (for example in the headspace of a reactor). Preferably, the gas atmosphere comprises an inert gas and/or hydrogen (H.sub.2 and/or .sup.xH.sub.2) optionally in the presence of O.sub.2. Preferred inert gases include nitrogen, argon, helium, neon, krypton, xenon, radon and sulfur hexafluoride (SF.sub.6) and mixtures thereof, more preferably nitrogen and/or argon, most preferably nitrogen. When the gas atmosphere comprises hydrogen (H.sub.2 or .sup.xH.sub.2), the hydrogen is preferably present at a concentration of 1-100%, with the remaining gas comprising an inert gas as defined herein and/or O.sub.2. Preferred gas atmospheres include from 80-100% H.sub.2 with the remaining gas comprising one or more inert gases; and from 0-20% H.sub.2 with the remaining gas comprising one or more inert gases and/or 02 (such as from 1-4% H.sub.2 in air). The gas atmosphere may optionally also include non-inert gases such as ammonia, carbon dioxide and hydrogen sulphide. Preferably, however, the gas atmosphere is free of ammonia, carbon dioxide and hydrogen sulphide.
[0290] The methods of the invention are typically conducted in an aqueous composition which may optionally comprise e.g. buffer salts. For some applications buffers are not required and the methods of the invention can be conducted without any buffering agents. Preferred buffer salts which can be used in the methods of the invention include Tris; phosphate; citric acid/Na.sub.2HPO.sub.4; citric acid/sodium citrate; sodium acetate/acetic acid; Na.sub.2HPO.sub.4/NaH.sub.2PO.sub.4; imidazole (glyoxaline)/HCl; sodium carbonate/sodium bicarbonate; ammonium carbonate/ammonium bicarbonate; MES; Bis-Tris; ADA; aces; PIPES; MOPSO; Bis-Tris Propane; BES; MOPS; TES; HEPES; DIPSO; MOBS; TAPSO; Trizma; HEPPSO; POPSO; TEA; EPPS; Tricine; Gly-Gly; Bicine; HEPBS; TAPS; AMPD; TABS; AMPSO; CHES; CAPSO; AMP; CAPS and CABS. Selection of appropriate buffers for a desired pH is routine to those skilled in the art, and guidance is available at e.g. http://www.sigmaaldrich.com/life-science/core-bioreagents/biological-buffers/learning-center/buffer-reference-center.html. Buffer salts used can be .sup.xH-labelled, for example by exchanging labile protons for .sup.xH.sup.+ ions by dissolving the salt in an .sup.xH-labelled solvent and subsequent solvent removal. Buffer salts are preferably used at concentrations of from 1 mM to 1 M, preferably from 10 mM to 100 mM such as about 50 mM in solution. Most preferred buffers for use in methods of the invention include 50 mM Tris-HCl, p(.sup.xH) 8.0.
[0291] The methods of the invention are typically conducted in an aqueous composition. However, non-aqueous components can optionally be used instead or as well as water in the compositions used in the methods of the invention. For example, the compositions comprising .sup.xH.sup.+ ions may optionally comprise one or more organic solvents (e.g. alcohols) or one or more ionic liquids.
[0292] The methods of the invention can be used to make an oxidised labelled cofactor from a reduced labelled cofactor. Such methods involve the production of a singularly or doubly .sup.xH-labelled reduced cofactor using methods of the invention as described herein and then removal of the non-required .sup.1H.sup. or .sup.xH.sup. using an appropriate NADH-dependent enzyme to yield the oxidised labelled cofactor. This method is illustrated schematically in
[0293] For example, the method of the invention can be used to label an unlabelled cofactor to produce 4S-labelled reduced cofactor e.g. (4S-.sup.xH)-NADH. Selective oxidation with an S-selective oxidoreductase, such as an (S)-selective alcohol dehydrogenase, leaves a labelled oxidised cofactor, e.g. (4-.sup.xH)-NAD.sup.+. Further reaction of the labelled NAD.sup.+ according to the methods of the invention can lead to a doubly .sup.xH-labelled reduced cofactor at the 4-position.
[0294] When the methods of the invention comprise producing a reduced labelled reaction product comprising one or more .sup.xH atom, the at least one enzyme that is an NADH-dependent oxidoreductase or an NADPH-dependent oxidoreductase or a functional derivative or fragment thereof is preferably at least one of an NAD(P)H-dependent alcohol dehydrogenase, an NAD(P)H-dependent ene reductase, an NAD(P)H-dependent imine reductase or an NAD(P)H-dependent amino-acid dehydrogenase. Other suitable NADH-dependent oxidoreductase or NADPH-dependent oxidoreductase enzymes include dehydrogenase, reductase, oxidase, synthase, transhydrogenase, dioxygenase and/or ene reductase enzymes. More preferably, the NADH-dependent oxidoreductase or NADPH-dependent oxidoreductase is at least one of an alcohol dehydrogenase or an amino acid dehydrogenase. As those skilled in the art will appreciate, any suitable NAD(P)H-dependent enzyme can be used, and the enzyme can be modified or selected to be specific for the desired reduction reaction. Variants, derivatives and functional fragments of the aforementioned oxidoreductases are also embraced by the present invention. Variants, derivatives and functional fragments of the aforementioned oxidoreductases retain at least some of the activity/functionality of the native/wild-type enzyme. Preferably, variants, derivatives and functional fragments of the aforementioned oxidoreductases have increased/improved activity/functionality when compared to the native/wild-type enzyme.
[0295] When the methods of the invention comprise producing a reduced labelled reaction product comprising one or more .sup.xH atom, the at least one enzyme that is an NADH-dependent oxidoreductase or an NADPH-dependent oxidoreductase or a functional derivative or fragment thereof is preferably immobilised onto a support as defined herein. More preferably, the at least one enzyme that is an NADH-dependent oxidoreductase or an NADPH-dependent oxidoreductase or a functional derivative or fragment thereof is immobilised onto the same support as the first polypeptide and/or the electron source. Most preferably, the at least one enzyme that is an NADH-dependent oxidoreductase or an NADPH-dependent oxidoreductase or a functional derivative or fragment thereof is immobilised onto the same support as the first polypeptide and the electron source, as such configurations allow facile purification of the product by sedimentation, filtration, centrifugation, or the like as described herein.
[0296] The methods of the invention can be used to produce a variety of reduced labelled reaction products including alcohols, e.g. using alcohol dehydrogenases. For example, ketones, aldehydes, carboxylic acids and amino acids can be reduced to form labelled alcohols. Similarly imines can be reduced to form labelled amines, e.g. using imine reductases. Olefins (alkenes) can be reduced to alkane groups, e.g. using ene reductases. Labelled amines and amino acids can also be produced by reductive amination of ketones, e.g. using amine dehydrogenases or amino acid dehydrogenases.
[0297] Accordingly, in preferred embodiments of the methods of the invention, [0298] the composition comprising .sup.xH.sup.+ ions comprises .sup.2H.sub.2O or .sup.3H.sub.2O; and [0299] the oxidised cofactor is NAD.sup.+, NADP.sup.+, or a labelled version of NAD.sup.+ or NADP.sup.+ comprising at least one .sup.xH atom, wherein the .sup.xH atom is at the 4-position of the nicotinamide ring.
[0300] In more preferred embodiments of the methods of the invention, [0301] the composition comprising .sup.xH.sup.+ ions comprises .sup.2H.sub.2O or .sup.3H.sub.2O; [0302] the oxidised cofactor is NAD.sup.+, NADP.sup.+, or a labelled version of NAD.sup.+ or NADP.sup.+ comprising at least one .sup.xH atom, wherein the .sup.xH atom is at the 4-position of the nicotinamide ring. [0303] the first polypeptide is one or more of the amino acid sequences of any one of SEQ ID NOs 1 to 29 or 69 to 70, or an amino acid sequence having at least 60% homology (such as at least 70%, at least 80%, at least 90% or at least 95% homology) therewith; [0304] the electron source is a second polypeptide or a synthetic organic, inorganic or metallic oxidation catalyst or an electrode connected to an electrode controller; wherein optionally: [0305] the second polypeptide is one or more of the amino acid sequences of any one of SEQ ID NOs 30 to 68, or an amino acid sequence having at least 60% homology (such as at least 70%, at least 80%, at least 90% or at least 95% homology) therewith; and/or [0306] the synthetic oxidation catalyst comprises platinum, palladium, iridium, nickel, rhodium and/or ruthenium; or is frustrated Lewis pair catalyst; and/or [0307] the reductant is H.sub.2 or .sup.xH.sub.2 wherein x=2 or 3; and/or [0308] the electrode material comprises: [0309] carbon; and/or [0310] a metal or metal alloy selected from gold, silver, tungsten, iridium, platinum, palladium, copper, titanium, brass, and steel; and/or [0311] a material selected from titanium oxide, indium oxide, tin oxide, indium tin oxide [0312] and [0313] i) the electron source and the first polypeptide each comprise or are in electronic contact with [0314] an electronically conducting support; wherein optionally the support material comprises: [0315] carbon; and/or [0316] a metal or metal alloy selected from gold, silver, tungsten, iridium, platinum, palladium, copper, titanium, brass, and steel; and/or [0317] a material selected from titanium oxide, indium oxide, tin oxide, indium tin oxide; [0318] or [0319] ii) the first polypeptide and the second polypeptide constitute component parts of a modular, multidomain or multicomponent protein or protein complex.
[0320] In still more preferred embodiments of the methods of the invention, [0321] the composition comprising H ions comprises .sup.2H.sub.2O; [0322] the oxidised cofactor is NAD.sup.+ or a labelled version of NAD.sup.+ comprising at least one .sup.xH atom, wherein the .sup.xH atom is at the 4-position of the nicotinamide ring; [0323] the first polypeptide is the HoxHYFU tetramer of Ralstonia eutropha (SEQ ID NOs: 1, 2, 30, 31), or an amino acid sequence having at least 60% homology (such as at least 70%, at least 80%, at least 90% or at least 95% homology) therewith; wherein optionally the HoxH moiety is a non-functional variant comprising the point mutation I64A (SEQ ID NO: 69); [0324] the electron source is a second polypeptide or a synthetic organic, inorganic or metallic oxidation catalyst, or an electrode connected to an electrode controller; wherein optionally: [0325] the second polypeptide is one or more of the amino acid sequences of any one of SEQ ID NOs 30-31, 37-40, 53-54 and/or 60-65, or an amino acid sequence having at least 80% homology (such as at least 90% or at least 95% homology) therewith; and/or [0326] the synthetic oxidation catalyst comprises platinum; and [0327] the reductant is H.sub.2; and/or [0328] the electrode material comprises carbon; [0329] and [0330] i) the electron source and the first polypeptide each comprise or are in electronic contact with the same electronically conducting support; wherein optionally the support material comprises carbon [0331] or [0332] ii) the first polypeptide and the second polypeptide constitute component parts of a modular, multidomain or multicomponent protein or protein complex.
[0333] The invention also provides a system for performing a method of the invention, the system comprising: [0334] i) a composition comprising (i) .sup.xH.sup.+ ions wherein x is 2 or 3; and (ii) an oxidised cofactor, wherein preferably the oxidised cofactor and/or the composition is as defined herein; [0335] ii) an electron source, wherein preferably the electron source is as defined herein; and [0336] iii) a first polypeptide which is an NADH:acceptor oxidoreductase or an NADPH:acceptor oxidoreductase or a functional derivative or fragment thereof, wherein preferably the first polypeptide is as defined herein;
[0337] wherein the system is configured such that, in use, (a) electrons are transferred from the electron source to the first polypeptide and (b) .sup.xH.sup.+ ions and the oxidised cofactor are contacted with the first polypeptide so as to reduce the oxidised cofactor to form a reduced labelled cofactor comprising one or more .sup.xH atoms.
[0338] The following Examples illustrate the invention. They do not, however, limit the invention in any way. In this regard, it is important to understand that the particular assays used in the Examples section are designed only to provide an indication of the efficacy of the method of the invention. There are many assays available to determine reaction efficiency and labelling success, and a negative result in any one particular assay is therefore not determinative.
EXAMPLES
[0339] Protein Expression
[0340] Methods for expression of proteins in cellular (e.g. microbial) expression systems are well known and routine to those skilled in the art. For example, the first polypeptide and the second polypeptide (if present) can be independently isolated from their host organisms using routine purification methods. For example, host cells can be grown in a suitable medium. Lysing of cells allows internal components of the cells to be accessed. Membrane proteins can be solubilised with detergents such as Triton X (e.g. Triton X-114, (1,1,3,3-Tetramethylbutyl)phenyl-polyethylene glycol, available from Sigma Aldrich). Soluble or solubilized proteins can be isolated and purified using standard chromatographic techniques such as size exclusion chromatography, ion exchange chromatography and hydrophobic interaction chromatography. Alternatively, the first polypeptide and the second polypeptide (if present) can be independently encoded in one or more nucleotide vector and subsequently expressed in an appropriate host cell (e.g. a microbial cell, such as E. coli). Purification tags such as a HIS (hexa-histidine) tag can be encoded (typically at the C- or N-terminal of the relevant polypeptide) and can be used to isolate the tagged protein using affinity chromatography for example using nickel- or cobalt-NTA chromatography. If desired, protease recognition sequences can be incorporated between the first and/or second polypeptide and the affinity purification tag to allow the tag to be removed post expression. Such techniques are routine to those skilled in the art and are described in, for example, Sambrook et al, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press.
[0341] Sequence Homology
[0342] Standard methods in the art may be used to determine homology. For example the UWGCG Package provides the BESTFIT program which can be used to calculate homology, for example used on its default settings (Devereux et al (1984) Nucleic Acids Research 12, p 387-395). The PILEUP and BLAST algorithms can be used to calculate homology or line up sequences (such as identifying equivalent residues or corresponding sequences (typically on their default settings)), for example as described in Altschul S. F. (1993) J Mol Evol 36:290-300; Altschul, S. F et al (1990) J Mol Biol 215:403-10). Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information (http://www.ncbi.nlm.nih.gov/).
[0343] Similarity can be measured using pairwise identity or by applying a scoring matrix such as BLOSUM62 and converting to an equivalent identity. Since they represent functional rather than evolved changes, deliberately mutated positions would be masked when determining homology. Similarity may be determined more sensitively by the application of position-specific scoring matrices using, for example, PSIBLAST on a comprehensive database of protein sequences. A different scoring matrix could be used that reflect amino acid chemico-physical properties rather than frequency of substitution over evolutionary time scales (e.g. charge). Conservative substitutions replace amino acids with other amino acids of similar chemical structure, similar chemical properties or similar side-chain volume. The amino acids introduced may have similar polarity, hydrophilicity, hydrophobicity, basicity, acidity, neutrality or charge to the amino acids they replace. Alternatively, the conservative substitution may introduce another amino acid that is aromatic or aliphatic in the place of a pre-existing aromatic or aliphatic amino acid. Conservative amino acid changes are well-known in the art and may be selected in accordance with the properties of the 20 main amino acids as defined in Table A below. Where amino acids have similar polarity, this can also be determined by reference to the hydropathy scale for amino acid side chains in Table B.
TABLE-US-00001 TABLE A Chemical properties of amino acids Ala aliphatic, hydrophobic, neutral Met hydrophobic, neutral Cys polar, hydrophobic, neutral Asn polar, hydrophilic, neutral Asp polar, hydrophilic, charged () Pro hydrophobic, neutral Glu polar, hydrophilic, charged () Gln polar, hydrophilic, neutral Phe aromatic, hydrophobic, neutral Arg polar, hydrophilic, charged (+) Gly aliphatic, neutral Ser polar, hydrophilic, neutral His aromatic, polar, hydrophilic, charged (+) Thr polar, hydrophilic, neutral Ile aliphatic, hydrophobic, neutral Val aliphatic, hydrophobic, neutral Lys polar, hydrophilic, charged(+) Trp aromatic, hydrophobic, neutral Leu aliphatic, hydrophobic, neutral Tyr aromatic, polar, hydrophobic
TABLE-US-00002 TABLE B Hydropathy scale Side Chain Hydropathy Ile 4.5 Val 4.2 Leu 3.8 Phe 2.8 Cys 2.5 Met 1.9 Ala 1.8 Gly 0.4 Thr 0.7 Ser 0.8 Trp 0.9 Tyr 1.3 Pro 1.6 His 3.2 Glu 3.5 Gln 3.5 Asp 3.5 Asn 3.5 Lys 3.9 Arg 4.5
[0344] Preferably, sequence homology can be assessed in terms of sequence identity. Any of a variety of sequence alignment methods can be used to determine percent identity, including, without limitation, global methods, local methods and hybrid methods, such as, e.g., segment approach methods. Protocols to determine percent identity are routine procedures within the scope of those skilled in the art. Global methods align sequences from the beginning to the end of the molecule and determine the best alignment by adding up scores of individual residue pairs and by imposing gap penalties. Preferred methods include CLUSTAL W (Thompson et al., Nucleic Acids Research, 22(22) 4673-4680 (1994)) and iterative refinement (Gotoh, J. Mol. Biol. 264(4) 823-838 (1996)). Local methods align sequences by identifying one or more conserved motifs shared by all of the input sequences. Preferred methods include Match-box, (Depiereux and Feytmans, CABIOS 8(5) 501-509 (1992)); Gibbs sampling, (Lawrence et al., Science 262(5131) 208-214 (1993)); and Align-M (Van Walle et al., Bioinformatics, 20(9) 1428-1435 (2004)). Thus, percent sequence identity is determined by conventional methods. See, for example, Altschul et al., Bull. Math. Bio. 48: 603-16, 1986 and Henikoff and Henikoff, Proc. Natl. Acad. Sci. USA 89:10915-19, 1992. Briefly, two amino acid sequences are aligned to optimize the alignment scores using a gap opening penalty of 10, a gap extension penalty of 1, and the blosum 62 scoring matrix of Henikoff and Henikoff (ibid.) as shown below (amino acids are indicated by the standard one-letter codes).
TABLE-US-00003 Alignment scores for determining sequence identity A R N D C Q E G H I L K M F P S T W Y V A 4 R 1 5 N 2 0 6 D 2 2 1 6 C 0 3 3 3 9 Q 1 1 0 0 3 5 E 1 0 0 2 4 2 5 G 0 2 0 1 3 2 2 6 H 2 0 1 1 3 0 0 2 8 I 1 3 3 3 1 3 3 4 3 4 L 1 2 3 4 1 2 3 4 3 2 4 K 1 2 0 1 3 1 1 2 1 3 2 5 M 1 1 2 3 1 0 2 3 2 1 2 1 5 F 2 3 3 3 2 3 3 3 1 0 0 3 0 6 P 1 2 2 1 3 1 1 2 2 3 3 1 2 4 7 S 1 1 1 0 1 0 0 0 1 2 2 0 1 2 1 4 T 0 1 0 1 1 1 1 2 2 1 1 1 1 2 1 1 5 W 3 3 4 4 2 2 3 2 2 3 2 3 1 1 4 3 2 11 Y 2 2 2 3 2 1 2 3 2 1 1 2 1 3 3 2 2 2 7 V 0 3 3 3 1 2 2 3 3 3 1 2 1 1 2 2 0 3 1 4
[0345] Percent identity is then calculated as:
100(T/L)
[0346] where
[0347] T=Total number of identical matches
[0348] L=Length of the longer sequence plus the number of gaps introduced into the longer sequence in order to align the two sequences
[0349] Materials and Reagents
[0350] General reagents and buffer salts (Sigma Aldrich), NAD.sup.+ and NADP.sup.+ (Prozomix), Pt/C (nominally 20 wt. %, Alfa Aesar), and carbon black particles (Black Pearls 2000, BP2000, Cabot Corporation), were all used as received without further purification. All non-deuterated solutions were prepared with MilliQ water (Millipore, 18 Mcm), and deuterated solutions with .sup.2H.sub.2O (99.98%, Sigma Aldrich). All solvents were deoxygenated by sparging with dry N.sub.2 for 60 minutes prior to use.
[0351] [.sup.2H.sub.5]-Tris..sup.2HCl was prepared by dissolving the required amount of Trizma base in .sup.2H.sub.2O and then evaporating to dryness. After repeating twice more, the pD (p.sup.2H) of the Tris solution was adjusted to 8.0 by the addition of small aliquots of .sup.2HCl (3.0 M). To preserve the isotopic purity of the buffer solution, the sample was deoxygenated with N.sub.2 that had first been bubbled through sacrificial .sup.2H.sub.2O. Comparison to the Tris peak (=3.70 ppm) in the .sup.1H NMR spectrum indicated that the final %.sup.2H.sub.2O was not below 99 mol. % (unless specifically diluted with .sup.1H.sub.2O).
[0352] pD (p.sup.2H) is measured as described in Covington et al. (Anal. Chem. (1968) 40 (4), 700-706).
[0353] Enzyme Purification and Isolation
[0354] R. eutropha soluble hydrogenase (SH; SEQ ID NOs: 1, 2, 3, 30, 31) was prepared as described in Lauterbach et al, FEBS J., 2013, 280, 3058-3068 and Lauterbach and Lenz, J. Am. Chem. Soc., 2013, 135, 17897-905. E. coli hydrogenase 1 (Hyd1, SEQ ID NOs: 37-38) and E. coli hydrogenase 2 (Hyd2; SEQ ID NOs: 39-40) were prepared as described in Lukey et al, J. Biol. Chem., 2010, 285, 3928-3938. R. eutropha NAD.sup.+ reductase (HoxFU, also referred to as NAD-R; SEQ ID NOs: 1, 2, 31, 69) was prepared as described in Lauterbach and Lenz, J. Am. Chem. Soc., 2013, 135, 17897-17905. Commercial samples of alcohol dehydrogenases (ADH101 and ADH105, Johnson Matthey Catalysis and Chiral Technologies), ene-reductase (ENE107, Johnson Matthey Catalysis and Chiral Technologies), L-alanine dehydrogenase (Sigma) were all received in their lyophilised forms and used without modification. ADH101 (Johnson Matthey Catalysis and Chiral Technologies) is a (R)-selective (pro-R) ketone reductase (alcohol dehydrogenase). ADH 105 (Johnson Matthey Catalysis and Chiral Technologies) is an (S) selective (pro-S) ketone reductase (alcohol dehydrogenase).
[0355] As discussed above, R. eutropha soluble hydrogenase (SH) comprises 4 subunits HoxHYFU, with HoxHY being related to H.sub.2/H.sup.+ cycling and HoxFU to NAD.sup.+/NADH. The HoxHY subunit is relatively unstable, but can be rendered obsolete by a single amino acid mutation (I64A) to a yield a more robust construct: HoxFU. HoxFUcan be considered to be a stabilised NAD.sup.+-reductase (diaphorase) suitable for coupling to various other external H.sub.2-oxidising systems, and is abbreviated to NAD-R for ease.
[0356] Catalyst Syntheses
[0357] All catalysts were prepared in a glovebox under a protective N.sub.2 atmosphere (O.sub.2<0.1 ppm), and in deoxygenated Tris-HCl (100 mM, pH 8.0). When the reaction was to be carried out under deuterated conditions, the non-isotopically enriched catalyst solution was centrifuged (12 000 rpm, 5 mins), decanted, and the solid re-suspended in an equal volume of [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM, pD 8.0).
[0358] Pt/C was prepared by sonication of a 20 mg/mL suspension for 515 minutes (with agitation of the solution in between). Suspensions of Pt/C were allowed to stand for between 15 minutes and 24 hours prior to use. For Pt+NAD-R/C, an aliquot of NAD.sup.+ reductase (1.4 mg/mL) was added to an equal volume of the Pt/C suspension and allowed to stand at 4 C. for 60 minutes prior to centrifugation (12 000 rpm, 5 mins), removal of the liquid, and re-suspension in the deuterated or non-deuterated buffer.
[0359] For experiments utilising carbon black, a suspension of BP2000 (20 mg/mL) was sonicated in the same manner as Pt/C. Particles of H2ase+NAD-R/C were then prepared by pre-mixing aliquots of the enzymes, and then adding them to a defined volume of BP2000. The H2ase+NAD-R/C particles then stood at 4 C. for 60 minutes, prior to centrifugation (12 000 rpm, 5 mins), removal of the excess solution, and re-suspension in the deuterated or non-deuterated buffer. Enzyme-modified particles were then used immediately, or snap-frozen in liquid N.sub.2 and stored at 80 C. prior to use. Whilst no attempt was made to quantify the degree of enzyme immobilisation, a considerable reduction in the brown hue of the solutions indicated that it was very high. If an additional enzyme (namely the NADH-dependent oxidoreductases) was to be co-immobilised on to the particles, this was done using a very large excess, after the particles had already been coated with H2ase and NAD-R.
[0360] Reaction Conditions
[0361] All reactions were set up in a glovebox under a protective N.sub.2 atmosphere (O.sub.2<0.1 ppm) and were conducted on a 500 L scale in sealed 1.5 mL micro-centrifuge tubes (Eppendorf) punctured with a single hole in the lid ( 1.0 mm). Solid catalysts were typically added at a loading of 100 g(C)/mL and SH was added at 20 L/mL. In order to help dissolve organic compounds such as AcPh, 2.0-5.0 vol. % (.sup.2H.sub.6)-dimethylsulphoxide was included in the reactions as required (with the deuterium label serving only to ease analysis, and playing no part in the reaction). The sealed tubes were then transferred to a Tinyclave pressure vessel (Buchi) and were charged with 2 bar partial pressures of .sup.1H.sub.2 or .sup.2H.sub.2 as required. The vessel was laid horizontally and rocked back and forth at 15 rpm whilst the reactions took place. Alternatively, a modified shaker was used that enabled a steady flow of the selected hydrogen gas across the reaction headspace with simultaneous agitation.
[0362] Product Analysis
[0363] Following depressurisation of the reaction vessel, the catalyst was separated from the reaction mixture by two rounds of centrifugations (10,000g, 5 mins) or by filtration through a nylon syringe filter (Gilson, 0.22 m). The solutions were then subject to one or more of the following analyses: H NMR spectroscopy, UV-Vis spectroscopy, high-performance liquid chromatography (HPLC), and gas chromatography (GC). The general methods for each of these techniques are described below:
[0364] .sup.1H NMR Spectroscopy
[0365] Following removal of the catalyst particles by filtration and centrifugation, 350-450 L of the sample solution was transferred to a Norell SelectSeries 5 mm 400 MHz sample tube. A further 50-150 L of .sup.2H.sub.2O was added for field locking purposes and, when required, 0.5 mM of acetone or 1.0 mM of 4,4-dimethyl-4-silapentane-1-sulfonic acid (DSS) was also included to act as a reference. .sup.1H NMR spectroscopy was carried out on either a Bruker Avance III HD nanobay (400 MHz) or Bruker Avance III (500 MHz) instrument, with samples for direct comparison always being run on the same machine. Both machines were equipped with 5 mm z-gradient broadband multinuclear probes. Spectra were acquired according to the parameters in the Table below. Data were acquired using either the standard Bruker .sup.1H 1D zg30 pulse program, or, for samples requiring solvent suppression, the noesygpprd program.
TABLE-US-00004 Machine Avance III - 400 Avance III - 500 Experiment .sup.1H .sup.1H RF pulse energy (MHz) 400.13 499.9 Temperature (K) 298 2 298 2 Number of scans 32 32 Pulse width (s) 14.0 10.3 Spectral width (Hz) 8000 8000 Acquisition time (s) 4.09 2.04 Relaxation delay (s) 1.00 2.00
[0366] In the first instance, the Bruker proc_Id or proc_1dakps processing algorithms were applied, followed by additional manual re-phasing where necessary. A multipoint baseline correction was also applied across the entirety of the spectral window and a line broadening corresponding to 0.3 Hz was applied to each spectrum to improve the S/N ratio. Signals were referenced against an internal acetone standard (=2.22 ppm), DMSO (=2.71), or the Tris peak (=3.70 ppm), all of which were referenced originally to DSS (=0.00 ppm).
[0367] The spectra of nicotinamide cofactors and their deuterated analogues were assigned according to well established literature arguments (see for example
[0368] HPLC
[0369] All HPLC was conducted on a Shimadzu UFLC LC-20AD prominence liquid chromatograph equipped with a dual wavelength UV-spectrophotometric detection. MilliQ water and HPLC grade solvents were used throughout. The following protocols were used depending on the nature of the analytes followed:
[0370] HPLC Method A
[0371] Description: Hydrophilic Interaction Liquid Chromatography (HILIC) for cofactor analysis
[0372] Sample: Samples were first filtered through a nylon syringe filter (Gilson, 0.22 m), and then centrifuged at 14,000 rpm for 5 minutes to remove any smaller particulates. 50 vol. % MeCN was added to the samples, prior to an additional round of centrifugation and transfer to glass HPLC vials.
[0373] Column: SeQuant ZIC-HILIC, 5 M particle size, 200 pore size, 1504.6 mm bed, equipped with a 202.1 mm guard
[0374] Buffer A: 90 vol. % MeCN (Honeywell, CHROMASOLV 99.9%): 10 vol. % MilliQ, 20 mM ammonium acetate, pH 7.5
[0375] Buffer B: 100 vol. % MilliQ, 20 mM ammonium acetate, pH 7.5
[0376] Column temperature=40 C.
[0377] Flow rate=1 mL/min
[0378] Injection volume=10 L
[0379] Detection=260 and 340 nm
[0380] Pump Profile
TABLE-US-00005 Time (minutes) Solvent ratio (vol % A:vol % B) 0 .fwdarw. 1 100:0 1 .fwdarw. 31 100:0 .fwdarw. 20:80 (linear gradient) 31 .fwdarw. 33 20:80 33 .fwdarw. 35 100:0
[0381] HPLC Method B
[0382] Description: Chiral HPLC for resolution of stereoisomers
[0383] Sample: Samples were extracted with a 2volume of heptane: 2-propanol (99:1 vol/vol), and then centrifuged at 14,000 rpm for 5 minutes before being transferred to glass vials for HPLC.
[0384] Column: Chiralpak IA column (15 cm4.6 mm, 5 m particle size) equipped with a 202.1 mm guard column
[0385] Buffer: heptane: 2-propanol (99:1 vol/vol)
[0386] Column temperature=40 C.
[0387] Flow rate=1 mL/min
[0388] Injection volume=10 L
[0389] Detection=210 nm
[0390] Pump profile=isocratic over 15 minutes
[0391] GC
[0392] GC was carried out on a ThermoScientific Trace 1310 equipped with an autosampler.
[0393] Sample: Samples were extracted with a 2volume of ethyl acetate, and then centrifuged at 14,000 rpm for 5 minutes before being transferred to glass vials for GC.
[0394] Column: DB-1701 (agilent), 30 m length, 0.25 mm diameter, 0.25 m (film thickness)
[0395] Carrier: He (CP grade), 0.5 mL minute (constant flow)
[0396] Detection: FID (H.sub.2=25 mL/min, air=350 mL/min, makeup N.sub.2=40 mL/min)
[0397] Oven Profile:
TABLE-US-00006 Time (minutes) Oven 0 .fwdarw. 2 Hold at 40 C. 2 .fwdarw. 23 Ramp to 250 C. at 10 C./min 23 .fwdarw. 33 Hold at 250 C. for 10 mins
[0398] UV-Vis Spectroscopy Reactions which resulted in changes in the relatative concentration of NAD(P).sup.+/NAD(P)H could be followed be UV-vis spectroscopy. Typically, solid particulates were removed from the solution by filtration or centrifugation (as described above) and the sample diluted in MilliQ (.sup.1H.sub.2O) water so that the cofactors were in the range 0.1-0.2 mM. A background spectrum of pure MilliQ was subtracted from that acquired for the sample. Measurements were made in a quartz cuvette (path length 1 cm, Hellma) on a Cary 60 UV/Vis spectrophotometer (Agilent). The ratio of NAD to NADH could then be determined by measuring the ratio of A.sub.260 nm: A.sub.340 nm.
Example 1
[0399] Examples 1A-1C demonstrate the method of the invention with the electron source being a second polypeptide and the first and second polypeptides not being component parts of an enzyme complex.
Example 1A
[0400] Carbon particles were modified with NAD.sup.+-reductase (NAD-R, i.e. R. eutropha soluble hydrogenase with an inactivated hydrogenase moiety, I64A, SEQ ID NOs: 1, 2, 31, 69) as the first polypeptide and E. coli hydrogenase 2 (SEQ ID NOs: 39-40) as the second polypeptide, as described above. The NAD.sup.+-reductase and hydrogenase are not native redox partners in vivo. Enzymes were not exchanged into deuterated buffer. Enzymes were prepared following standard protocols. Carbon particles (Black Pearls 2000) were prepared by sonication for 90 minutes in [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM, p.sup.2H 8.0) at a concentration of 20 mg mL.sup.1. A mixture of the hydrogenase and NAD.sup.+-reductase (each of a concentration of between 1-2 mg/mL) was added to an aliquot of carbon particles and left at 4 C. for 90 minutes. The particles were then centrifuged (12 000 rpm, 2 mins) and the supernatant removed and replaced with sufficient .sup.2H-Tris..sup.2HCl to give a concentration of 10 mg(C)/mL. Enzyme loading was determined as 3-5 g of each enzyme per 100 g(C) (assuming enzymes were fully immobilised).
[0401] An aliquot containing 100 g of enzyme modified particles was then added to 500 L of [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM in .sup.2H.sub.2O, p.sup.2H 8.0) containing 1.0 mM NAD.sup.+, which had been pre-saturated with .sup.1H.sub.2 gas. The reaction solution was subsequently sealed in a pressure vessel under 2 bar of .sup.1H.sub.2 and rocked at 15 rpm for 18 hours at 20 C.
[0402] Production of reduced cofactor (NADH) was monitored by UV-Visible spectroscopy with the characteristic peak observed at 340 nm indicative of formation of the reduced cofactor. Confirmation of the isotopic composition of the NADH was made by .sup.1H NMR spectroscopy. The general procedures for these methods are described above.
[0403] UV-visible spectra (
[0404] .sup.1H NMR spectroscopy (
[0405] The .sup.1H NMR spectra shown in
Example 1B
[0406] The reaction was conducted in a similar manner to that described in Example 1A, but using E. coli hydrogenase 1 (SEQ ID NOs: 37-38) as the second polypeptide.
[0407] In brief, the following conditions were used: 100 g(C) with 15-20 g of immobilised hydrogenase (E. coli hydrogenase 1) and NAD.sup.+ reductase (NAD-R, SEQ ID NOs: 1, 2, 31, 69) was suspended in 500 L [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM in .sup.2H.sub.2O, p.sup.2H 8.0) containing 4 mM NAD.sup.+ which had been pre-saturated with .sup.1H.sub.2 gas. The reaction solution was subsequently sealed in a pressure vessel under 2 bar of .sup.1H.sub.2 and rocked at 30 rpm for 16 hours at 20 C.
[0408] Product analysis as described in Example 1A showed high conversion (>95%) to NADH, with high selectivity (>95%) for the [4S-.sup.2H]-NADH isotopomer (see
[0409] The .sup.1H NMR spectra shown in
Example 1C
[0410] The reaction was conducted in a similar manner to that described in Example 1A, but using E. coli hydrogenase 1 (SEQ ID NOs: 37-38) as the second polypeptide and HoxF NAD.sup.+ reductase (SEQ ID NO: 1) as the first polypeptide.
[0411] In brief, the following conditions were used: 200 g(C) with 40 g of immobilised hydrogenase and NAD.sup.+ reductase was suspended in 800 L [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM in .sup.2H.sub.2O, p.sup.2H 8.0) containing 3.5 mM NAD.sup.+ which had been pre-saturated with .sup.1H.sub.2 gas. The reaction solution was subsequently sealed in a shaker plate under a steady stream of .sup.1H.sub.2 and shaken at 500 rpm for 16 hours at 20 C.
[0412] Product analysis as described in Example 1A showed a conversion of around 60% to NADH, with high selectivity (>95%) for the [4S-.sup.2H]-NADH isotopomer (see
[0413] The .sup.1H NMR spectra shown in
Example 2
[0414] This Example demonstrates the method of the invention with the electron source being a second polypeptide and the first and second polypeptides being component parts of an enzyme complex.
[0415] R. eutropha soluble hydrogenase (SEQ ID NOs: 1, 2, 3, 30, 31) was placed in 500 L [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM in .sup.2H.sub.2O, p.sup.2H 8.0) containing 1 mM NAD.sup.+. The reaction solution was subsequently sealed in a pressure vessel under 2 bar of .sup.1H.sub.2 and rocked at 15 rpm for 15 hours at 20 C.
[0416] Product analysis as described in Example 1A showed high conversion (>95%) to NADH, with high selectivity (>95%) for the [4S-.sup.2H]-NADH isotopomer (see
[0417] The .sup.1H NMR spectra shown in
Example 3
[0418] This Example demonstrates the method of the invention with the electron source being a carbon electrode.
[0419] R. eutropha soluble hydrogenase with inactive hydrogenase (NAD-R, SEQ ID NOs: 1, 2, 31, 69) was immobilised on carbon particles (Black Pearls 2000) as described in Example 1A. The carbon particles were then immobilised on a 3 mm diameter pyrolytic graphite edge rotating disk electrode (see Lauterbach et al, PLoS ONE; doi:10.1371/journal.pone.0025939). The enzyme-modified particles were deposited on the electrode and allowed to partially dry over ca 2 minutes before submersing into the electrochemical cell.
[0420] The modified electrode was placed in an electrochemical cell containing NAD.sup.+ (10 mM) in 5 mL [.sup.2H]-Tris..sup.2HCl (100 mM in .sup.2H.sub.2O, p.sup.2H 8.0) and rotated at 1000 rpm. The electrode was held at 0.75 V vs SCE (SCE=saturated calomel electrode; SCE=+0.248V vs SHE at 20 C.) for 16 hours. At this potential, no direct reduction of the cofactor at the electrode is observed.
[0421] Product analysis as described in Example 1A showed a conversion of around 50% to NADH, with high selectivity (>95%) for the [4S-.sup.2H]-NADH isotopomer (see
[0422] The .sup.1H NMR spectra shown in
Example 4
[0423] This Example demonstrates the method of the invention for the generation of labelled-NADPH, with the electron source being a second polypeptide and the first and second polypeptides not being component parts of an enzyme complex.
[0424] The reaction was conducted in a similar manner to that described in Example 1A, but using E. coli hydrogenase 2 (SEQ ID NOs: 39-40) as the second polypeptide and HoxHYFE.sup.341A+D467SU (SEQ ID NOs: 2, 30, 31, 70) as the first polypeptide.
[0425] The following conditions were used: 100 g(C) with 6 g of immobilised hydrogenase and 10 g of immobilised NAD.sup.+ reductase was suspended in 300 L [.sup.2H.sub.5]-Tris..sup.2HCl (50 mM in .sup.2H.sub.2O, p.sup.2H 8.0) containing 5 mM NADP.sup.+ which had been pre-saturated with .sup.1H.sub.2 gas. The reaction solution was subsequently sealed in a pressure vessel under 2 bar of .sup.1H.sub.2 and rocked at 30 rpm for 16 hours at 20 C.
[0426] Product analysis as described in Example 1A showed a conversion of around 20% to NADPH, with high selectivity (>95%) for the [4S-.sup.2H]-NADPH isotopomer (see
[0427] The .sup.1H NMR spectra shown in
Example 5
[0428] This Example provides a systematic comparison of various embodiments of the methods of the invention for production of [4-.sup.2H]-NADH. Catalysts were screened for activity in converting NAD.sup.+ to [.sup.2H]-NADH under various reaction conditions.
[0429] Experiments were carried out to screen the selectivity of H.sub.2-driven NAD.sup.+ reduction by the routes illustrated in
[0430] The heterogeneous catalysts were prepared as dispersions in aqueous buffer solution by sonication of either Pt/C (nominally 20 wt. %, Alfa Aesar) or carbon black (Black Pearls 2000, Cabot) at 20 mg mL.sup.1. Enzyme-modified particles were prepared by pre-mixing the required enzyme solutions before adding dispersed carbon particle solution as described in Example 1A. The particle-enzyme solutions were left at 4 C. for enzyme immobilisation. The heterogeneous systems were compared to a native enzyme, R. eutropha soluble hydrogenase (SEQ ID NOs: 1, 2, 30, 31), which was added to reactions in solution.
[0431] The catalysts were injected into .sup.xH.sub.2-saturated solution containing NAD.sup.+ (4-5 mM) and left under 2 bar .sup.xH.sub.2 for 16 hours. The reactions were analysed using a combination of UV-vis spectroscopy, HPLC and NMR as described in Example 1A. Experiments were carried out on a small scale (500 L) with low catalyst loading (100 g carbon mL.sup.1). The mass of NAD reductase exposed to the carbon particles was kept constant and unabsorbed enzyme was removed by centrifugation before use.
[0432] Initial experiments were performed in protiated solvent (.sup.1H.sub.2O) and diprotium gas (.sup.1H.sub.2) to evaluate the selectivity of the catalysts towards the formation of 4-NADH. For each system the chemo-selectivity refers to the concentration of 4-NADH generated relative to the loss of NAD.sup.+, as determined from HPLC traces (Table 1, Entries 1-4). Whilst the conversion of NAD.sup.+ was of a similar magnitude for all catalysts (usually 60-90%), the selectivity towards the formation of the desired 4-NADH was highly variable for the Pt/C system. For this latter case, yellowing of the reaction solution and appearance of extra peaks in subsequent HPLC analysis were evidence of the formation of biologically inactive side products (likely including NAD.sub.2 dimers, 2-/6-NADH, and over-reduced compounds) (
[0433] The Pt+NAD-R/C system also shows high selectivity for 4-NADH. This is particularly noteworthy, suggesting that there is rapid electron transfer from H.sub.2 oxidation at Pt through the carbon particle to the NAD.sup.+ reductase for selective NAD.sup.+ reduction and that no unselective NAD.sup.+ reduction at Pt occurs.
[0434] Analogous experiments were performed for each catalyst system with the same diprotium gas (.sup.1H.sub.2) as the reductant, but with deuterated solvent, .sup.2H.sub.2O (Table 1, Entries 5-8). The same selectivity as observed for NAD.sup.+ reduction in .sup.1H.sub.2O was recorded. The extent of .sup.2H incorporation to generate [4-.sup.2H]-NADH was analysed using NMR (
[0435] The high level of .sup.2H incorporation observed for the Pt+NAD-R/C system further supports the observation that electrons from H.sub.2 oxidation at Pt are rapidly transferred to the NAD.sup.+ reductase for NAD.sup.+ reduction as both the chemo and isotopic selectivity of the NAD.sup.+ reductase are conserved.
TABLE-US-00007 TABLE 1 Catalyst screening for conversion of NAD.sup.+ to [4-.sup.2H]-NADH Entry Catalyst Reductant Solvent.sup.(c) 1 Pt/C .sup.1H.sub.2 .sup.1H.sub.2O 2 Pt + NAD.sup.+ reductase/C 3 Hydrogenase + NAD.sup.+reductase/C 4.sup.(b) Soluble hydrogenase 5 Pt/C .sup.1H.sub.2 .sup.2H.sub.2O 6 Pt + NAD.sup.+ reductase/C 7 Hydrogenase + NAD.sup.+reductase/C 8.sup.(b) Soluble hydrogenase % Chemo- % Isotopic- % Stereo- Yield/ Entry % Conversion.sup.(d) selectivity.sup.(e) selectivity.sup.(f) selectivity.sup.(g) mM.sup.(h) 1 80 85 2 90 100 3 90 100 4.sup.(b) 90 100 5 80 85 65 54 1.0 6 90 100 100 98 3.6 7 90 100 100 100 3.6 8.sup.(b) 90 100 100 100 4.5
[0436] Reactions conducted on 500 L scale with 4 mM NAD under 2 bar gas pressure for 16 hours and rocking at 15 rpm (unless otherwise specified); (b) 5 mM NAD.sup.+; (c) .sup.1H.sub.2O=Tris-HCl (100 mM, pH 8.0), .sup.2H.sub.2O=d.sub.5-[.sup.2H.sub.5]-Tris..sup.2HCl (100 mM, pD 8.0); (d) Conversion refers to loss of NAD.sup.+, as determined by HPLC; (e) chemo-selectivity reported as the percentage of 4-NADH compared to the loss of NAD.sup.+, as determined by HPLC; (f) isotopic-selectivity reported as the percent of labelled 4-NADH compared to total 4-NADH, as determined by NMR; (g) stereo-selectivity for [4S-.sup.2H]-NADH compared to labelled 4-NADH, as determined by NMR; (h) overall yield of [4S-.sup.2H]-NADH. Representative HPLC and NMR traces are shown in
[0437] As expected, the results in Table 1 confirm that bare Pt shows very poor selectivity towards 4-NADH under any conditions. The results in Table 1 show that much higher yields of [4S-.sup.2H]-NADH are achieved using the Pt+NAD-R/C, H2ase+NAD-R/C and soluble hydrogenase systems according to the methods of the invention than are achieved using the purely chemical Pt/C system.
[0438] The reduced labelled cofactor, [4-.sup.2H]-NADH, can be formed as either the R- or S-stereoisomer, and the stereochemistry of the reduced cofactor can be assigned using NMR as described above. The results summarised in Table 1 demonstrate that the purely chemical Pt/C system gives a roughly racemic product. By contrast, all the systems using the NAD.sup.+ reductase for NAD.sup.+ reduction in accordance with the methods of the invention selectively generate [4S-.sup.2H]-NADH.
[0439] Without being bound by theory, the inventors believe that the stereoselectivity of the biological systems using NAD.sup.+ reductase for NAD.sup.+ reduction in accordance with the methods of the invention is a consequence of the structure of the active site of the enzyme. Inspection of the crystal structure of the structurally similar protein, Complex 1 from Thermus thermophilus (Tt) and comparison with a homology model of the R. eutropha HoxFU protein (SEQ ID NOs: 1, 2) (
Example 6
[0440] This Example confirms that the isotopic composition of the reaction medium (rather than the reductant) determines the isotopic composition of the reaction product.
[0441] The mechanisms of [4-.sup.xH]-NADH generation by the heterogeneous systems described in Example 5 were further probed by comparing .sup.xH incorporation under either .sup.1H.sub.2 or .sup.2H.sub.2 in a series of .sup.1H.sub.2O:.sup.2H.sub.2O mixtures (100:0, 75:25, 50:50, 25:75, and 0:100 v/v %).
[0442] Experiments compared reduction of NAD by (i) Pt/C (platinum supported on carbon); (ii) Pt+NAD-R/C (platinum and NAD.sup.+ reductase (SEQ ID NOs: 1, 2, 31, 69) supported on carbon) and (iii) H2ase+NAD-R/C (E. coli hydrogenase 1 (SEQ ID NOs: 37-38) and NAD.sup.+ reductase (SEQ ID NOs: 1, 2, 31, 69) supported on carbon). The isotopic selectivity under a number of .sup.xH.sub.2 and .sup.xH.sub.2O conditions is reported in
[0443] The required solution were prepared by mixing solutions of Tris-HCl (100 mM, pH 8.0) in .sup.1H.sub.2O with [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM, pD 8.0) in .sup.2H.sub.2O in the appropriate volumes. The catalysts were injected into .sup.xH.sub.2-saturated solution containing NAD.sup.+ (4 mM) and left under 2 bar .sup.xH.sub.2 for 16 hours. Experiments were carried out on a small scale (500 L) with low catalyst loading (100 g carbon mL). The reactions were analysed using a combination HPLC and NMR as described in Example 1A. The yield of reduced cofactor (of any isotopic composition) was between 50-90 mol % in all cases. The %.sup.2H incorporation was determined by comparison of the relative intensities of the peaks corresponding to [4S-.sup.2H]-NADH, [4R-.sup.2H]-NADH, and [4-.sup.1H.sub.2]-NADH in the .sup.1H NMR spectrum.
[0444] The results in
[0445] The results in
[0446] This Example thus shows that in the methods of the invention, the isotopic composition of the reaction medium (rather than the reductant) determines in all cases the isotopic composition of the reaction product. A desired ratio of labelled: unlabelled cofactor can therefore be achieved by controlling the isotopic composition of the reaction medium.
Example 7
[0447] This Example demonstrates that the methods of the invention can be used to supply labelled cofactor to a NAD(P)H-dependent oxidoreductase in order to generate a chemo- and stereo-selectively labelled product. Four examples are used to verify that the methods of the invention are capable of generating and recycling deuterium-labelled cofactors to drive two alcohol dehydrogenases (Johnson Matthey R-selective ADH101 and S-selective ADH 105), an ene reductase (Johnson Matthey ENE 107) and an amino acid dehydrogenase (Sigma L-alanine dehydrogenase) in the conversion of unlabelled substrate to labelled product.
[0448] Firstly, an R-selective ADH and an S-selective ADH (ADH101 and ADH105 respectively) were used to deliver a deuteride to opposing faces of acetophenone, thereby separately generating both enantiomers of [.sup.2H]-phenylethanol.
[0449] Reactions were carried out using around 100 g(C) catalyst with 10-20 g of E. coli hydrogenase 1 (SEQ ID NOs: 37-38) and I64A (SEQ ID NOs: 1, 2, 31, 69) prepared according to the methodologies in Example 1). The catalyst was added to 500 L of [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM, p.sup.2H 8.0) containing 0.1 mM NAD.sup.+, 10 mM acetophenone, and 5 vol. % [.sup.2H.sub.6]-DMSO pre-saturated with .sup.1H.sub.2 gas. 0.5 mg of the required alcohol dehydrogenase was then added and the reaction solution was sealed in a shaker plate under a steady stream of .sup.1H.sub.2 and shaken at 750 rpm for 20 hours at 20 C.
[0450] The reaction was analysed qualitatively by .sup.1H NMR and extracted into heptane for chiral HPLC (
[0451] A second reaction was tested employing an ene-reductase, to further demonstrate the chemoselectivity of the invention by the reduction of a CC in the presence of CO. In this reaction dimethyl itaconate was converted to dimethyl [2-.sup.2H]-2-([.sup.2H.sub.1]methyl) succinate. The reactions conditions were 200 g(C) catalyst with 5-10 g of E. coli hydrogenase 1 (SEQ ID NOs: 37-38) and I64A (SEQ ID NOs: 1, 2, 31, 69) co-immobilised on it (prepared as above). 500 L of [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM, p.sup.2H 8.0) containing 0.5 mM NAD.sup.+, 5 mM dimethyl itaconate, and 2 vol. % [.sup.2H.sub.6]-DMSO presaturated with .sup.1H.sub.2 gas charged with the catalyst. 0.5 mg of ene reductase was added and the reaction solution was sealed in a shaker plate under a steady stream of .sup.1H.sub.2 and shaken at 500 rpm for 16 hours at 20 C.
[0452] The reaction was analysed qualitatively by .sup.1H NMR and extracted into EtOAC for GC (
[0453] Finally, a reaction was conducted to demonstrate the ability of the catalyst in a reductive amination reaction, involving the conversion of an alpha-keto acid (pyruvate) to a deuterated amino acid ([2S-.sup.2H]-alanine). In these reactions 400 g(C) catalyst with 20-40 g of hydrogenase 1 (SEQ ID NOs: 37-38) and I64A (SEQ ID NOs: 1, 2, 31, 69) co-immobilised on it (prepared as above). 500 L of [.sup.2H.sub.11]-Tris..sup.2HCl (100 mM, p.sup.2H 8.0) containing 0.5 mM NAD.sup.+, 5 mM sodium pyruvate, and 25 mM NH.sub.4Cl was presaturated with .sup.1H.sub.2 gas and charged with the catalyst. 0.5 mg of L-alanine dehydrogenase was added and the reaction solution was sealed in a shaker plate under a steady stream of .sup.1H.sub.2 and shaken at 500 rpm for 16 hours at 20 C.
[0454] The reaction was analysed qualitatively by .sup.1H NMR. The absence of a multiplet peak at =3.83 ppm, and collapse of coupling in the peak at =1.45 ppm in the .sup.1H NMR spectrum (relative to .sup.1H-standard), are diagnostic of the correct isotopologue having been produced (see
[0455] A summary of the reactions demonstrated is shown in
Example 8
[0456] This Example demonstrates that the methods of the invention can be used to synthesize a range of labelled cofactors.
[0457] The results above demonstrate that the methods of the invention can selectively generate the S isomer of the deuterium labelled cofactor, (i.e. [4S-.sup.2H]-NADH, and that this cofactor can be used by an R-selective alcohol dehydrogenase (ADH) for reductive deuterium addition to a ketone. However, for a number of applications for examples in mechanistic studies it is desirable to have access to other deuterium labelled cofactors.
[0458]
[0459] The above methods were demonstrated using the H2ase+NAD-R/C system for selective NAD.sup.+ reduction. This system was chosen due to its selectivity and the ease of separation of the catalyst from the reaction mixtures. Any of the systems in accordance with the methods of invention can be used to generate the cofactors.
[0460] The general scheme shown in
[0461] The following conditions were used in the reactions (using
Step A: Synthesis of [4S-.SUP.2.H]-NADH from [4-.SUP.1.H]-NAD.SUP.+
[0462] 100 g(C) catalyst with 20-40 g of E. coli hydrogenase 1 (SEQ ID NOs: 37-38) and I64A (SEQ ID NOs: 1, 2, 31, 69) co-immobilised on it (prepared as previously) was added to 500 L of [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM, p.sup.2H 8.0) containing 4 mM NAD.sup.+, which had been presaturated with .sup.1H.sub.2 gas. The reaction solution was sealed under 2 bar H.sub.2 for 16 hours, whilst rocking at 30 rpm. Analysis by UV-spectrophotometry and .sup.1H NMR spectroscopy indicated complete conversion of the cofactor to the desired [4S-.sup.2H]-NADH form.
Step B: Synthesis of [4-.SUP.2.H]-NAD.SUP.+ from [4S-2.H]-NADH
[0463] Johnson Matthey alcohol dehydrogenase (ADH105) was immobilised on carbon particles by suspending a concentrated solution (20 mg/mL) in an equal volume of sonicated BP2000 particles (20 mg/mL) for 30 minutes at 4 C. Following centrifugation (12 000 rpm, 5 minutes) the supernatant was removed, and the particles washed once in 100 L .sup.2H.sub.2O. The ADH particles were then added to a deoxygenated solution of [4S-.sup.2H]-NADH (1 mL, 4 mM) in [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM, p.sup.2H 8.0), followed by neat acetophenone (10 mM), and the whole solution was shaken under N.sub.2 for a period of 5 days. The ADH particles were removed by centrifugation (12 000 rpm, 5 minutes) and the sacrificial acetophenone/phenylethanol removed by extraction with C.sup.2HCl.sub.3 (3500 L). Analysis by UV-spectrophotometry and .sup.1H NMR spectroscopy indicated >90% conversion of the cofactor to the desired [4-.sup.2H]-NAD.sup.+ form, with the absence of a doublet at =8.8 ppm being evidence of the labelling at the 4-position.
Step C: Synthesis of [4-.SUP.2.H.SUB.2.]-NADH from [4-.SUP.2.H]-NAD.SUP.+
[0464] Particles of the same constitution as Step A were added at a loading of 200 g(C)/mL to a solution of [4-.sup.2H.sub.2]-NADH (500 L, 3 mM) that had been pre-saturated with .sup.1H.sub.2 gas. The solution was then sealed under 2 bar H.sub.2 and rocked at 30 rpm for 16 hours. Analysis by UV-spectrophotometry and .sup.1H NMR spectroscopy indicated >90% conversion of the cofactor to the desired [4-.sup.2H.sub.2]-NAD.sup.+ form, with the relative absence of signals at =2.6-2.8 ppm being evidence of the complete labelling.
Step D: Synthesis of [4R-.SUP.2.H]-NADH from [4-.SUP.2.H]-NAD.SUP.+
[0465] A solution of [4-.sup.2H]-NAD.sup.+ (1 mL, 3 mM) in [.sup.2H.sub.5]-Tris..sup.2HCl (100 mM, p.sup.2H 8.0) was prepared according to Step B, except using free alcohol dehydrogenase (rather than immobilised). To the solution was added an equal volume of acetonitrile, and precipitated alcohol dehydrogenase removed by centrifugation (12 000 rpm, 5 minutes). The solution was gently evaporated to dryness on a rotary evaporator, and the solid re-dissolved in deionised .sup.1H.sub.2O. The evaporation and re-dissolution steps were repeated twice more. The solution was evaporated a final time, before being transferred to a glovebox and being re-dissolved in deoxygenated deionised .sup.1H.sub.2O (1 mL). The cofactor solution was subsequently saturated with .sup.1H.sub.2 gas. 200 gC catalyst with 30-40 g of E. coli hydrogenase 2 (SEQ ID NOs: 39, 40) and NAD.sup.+ reductase immobilised on the surface was added to solution, which was subsequently sealed under 2 bar H.sub.2 and shaken at 30 rpm for 18 hours. The carbon catalyst was removed by centrifugation (12 000 rpm, 5 minutes) and the solution analysed by UV-spectrophotometry and .sup.1H NMR spectroscopy. The analysis indicated around 60% conversion to the reduced cofactor, with a high selectivity (>90%) for the [4R-.sup.2H]-NADH form, as evidence by the signal at =2.66 ppm.
[0466] Each of the cofactors produced was analysed using UV-vis spectroscopy and NMR as described in Example 1A. Data are shown in
Example 9
[0467] This Example provides further verification that the methods of the invention can be used to supply labelled cofactor to a NAD(P)H-dependent oxidoreductase in order to generate a chemo- and stereo-selectively labelled product.
[0468] In the results discussed below, the %.sup.2H incorporation achieved at the target sites using this approach was between 93-99%. The demonstrated ability to work across diverse functional group space indicates the utilty of this approach to generate libraries of well-defined [.sup.2H]-labelled chiral building blocks, e.g. for fine chemical synthesis, for small molecules for analytical applications, or for later-stage deuteration of pharmaceutical precursors, particularly where biocatalysis is already implemented in the reaction sequence.
[0469] All experiments in this Example were conducted using the biocatalyst system of the invention with E. coli hydrogenase 1 (SEQ ID Nos: 37-38) and NAD.sup.+ reductase I64A (SEQ ID Nos: 1, 2, 31, 69) prepared as described above. Commercial enzymes were received in lyophilized form and used without further purification. Catalyst system was prepared by sonication of a 20 mg/mL suspension of BP2000 carbon black in Tris-HCl buffer for 515 minutes (with agitation of the solution in between). Equal volumes of hydrogenase (4 mg/mL) and NAD.sup.+ reductase (1.4 mg/mL) were then pre-mixed together, and added immediately to an aliquot of sonicated carbon. After standing at 4 C. for 60 minutes, the solid catalyst was then removed from the preparatory solution by centrifugation (10,000g, 5 mins) before being re-suspended in deuterated or non-deuterated buffer as required. Enzyme loadings: hydrogenase loading of 39 pmoles per 100 g of carbon, NAD.sup.+ reductase loading of 65 pmoles per 100 g of carbon.
[0470] Deuterated buffer (.sup.2H.sub.5)-Tris-.sup.2HCl was prepared by dissolving the required amount of Trizma base in .sup.2H.sub.2O and then evaporating to dryness. After repeating twice more, the pD (p.sup.2H) of the Tris solution was adjusted to 8.0 by the addition of small aliquots of .sup.2HCl (3.0 M) prior to deoxygenation by sparging with dry N.sub.2. Solutions of fully deuterated (.sup.2H.sub.11)-Tris-.sup.2HCl were also used for analytical purposes, and were prepared in a similar manner. .sup.1H NMR spectroscopy indicated that the final %.sup.2H.sub.2O of deuterated buffer solutions was not below 99 mol. % (unless specifically diluted with .sup.1H.sub.2O). Other conditions and analysis conducted as described above unless otherwise stated.
[0471] GC-FID was carried out on a ThermoScientific Trace 1310. GC-MS was carried out on an Agilent 7890B GC coupled to an Agilent 7200 Accurate Mass Q-ToF MS operating under EI mode. For both machines, injections were carried out by means of a robotic autosampler. The relevant columns and chromatography conditions are stated as required.
[0472] All HPLC was conducted on a Shimadzu UFLC LC-20AD Prominence liquid chromatograph equipped with a dual wavelength UV-spectrophotometric detector and a robotic autosampler. MilliQ water and HPLC grade solvents were used throughout. The relevant columns and chromatography conditions are stated as required.
Example 9.1
[0473] In this reaction pyruvate was converted to [2L-.sup.2H]-lactate. The reactions were conducted in 0.5 mL of (.sup.2H.sub.1)-Tris-.sup.2HCl (100 mM, p.sup.2H 8.0) containing 5 mM sodium pyruvate, 0.5 mM NAD.sup.+, and 500 g of L-lactate dehydrogenase (Merck). The mixture was presaturated with H.sub.2 gas prior to addition of the heterogeneous biocatalytic system at a loading of 400 g. The reactions were shaken at 500 rpm under a steady flow of H.sub.2 for 16 hours. The reaction was analysed by GC, MS and NMR.
[0474] GC-FID: analytes were first derivatised and then subjected to analysis by GC-FID. 100 L of reaction mixture was combined with 23 L of EtOH and 13 L of pyridine by means of a vortex mixer. Subsequently, 15 L of ethyl chloroformate was added, and the reaction allowed to proceed until no further CO.sub.2 was evolved. The derivatised pyruvate/lactate was extracted with 100 L of C.sup.2HCl.sub.3, and transferred to a glass vial for analysis by GC. Conditions as below:
[0475] Column: DB-1701 (Agilent), 30 m length, 0.25 mm diameter, 0.25 m film thickness; Carrier: He (CP grade), 1.1 mL minute (constant flow); Inlet temperature: 250 C.; Injection conditions: Splitless with split flow 50 mL/min, splitless time 0.7 mins, purge 5 mL/min; Injection volume: 0.5 L; Detection: FID; Detector temperature: 200 C.; Detection gases: H.sub.2 (35 mL/min), air (350 mL/min), makeup N.sub.2 (40 mL/min); Oven heating profile: [0476] 0-2 mins, Hold at 45 C. [0477] 2-15 mins, Ramp to 250 C. at 16 C./min [0478] 15-20 mins, Hold at 250 C. for 5 mins
[0479] Chiral GC-FID: The ee of the lactate product was determined by first derivatising with a chiral alcohol ((2R,3R)-()-2,3-butanediol) and then analysing the reaction solution by GC-FID. 100 L of reaction mixture was combined with 35 L of (2R,3R)-()-2,3-butanediol and 13 L of pyridine by means of a vortex mixer. Subsequently, 15 L of ethyl chloroformate was added, and the reaction allowed to proceed until no further CO.sub.2 was evolved. Commercial standards of L- and D-lactate were similarly derivatised for comparison. The derivatised analytes were then extracted with 100 L of C.sup.2HCl.sub.3, and transferred to a glass vial for analysis by GC. The formation of diastereomeric products allowed for the analysis to be conducted on an achiral GC column. Conditions as below:
[0480] Column: DB-1701 (Agilent), 30 m length, 0.25 mm diameter, 0.25 m film thickness; Carrier: He (CP grade), 170 kPa (constant pressure); Inlet temperature: 230 C.; Injection conditions: Splitless with split flow 50 mL/min, splitless time 0.7 mins, purge 5 mL/min; Injection volume: 0.5 L; Detection: FID;
[0481] Detector temperature: 250 C.; Detection gases: H.sub.2 (35 mL/min), air (350 mL/min), makeup N.sub.2 (40 mL/min); Oven heating profile:
TABLE-US-00008 Time (minutes) Temperature 0 .fwdarw. 5 Hold at 100 C. 5 .fwdarw. 30 Ramp to 150 C. at 2 C./min 30 .fwdarw. 35 Hold at 150 C. for 5 minutes .sup.35 .fwdarw. 41.5 Ramp to 280 C. at 2 C./min 41.5 .fwdarw. 46.5 Hold at 280 C. for 5 minutes
[0482] GC-MS: Following analysis by GC-FID the EtOH/ethyl chloroformate derivatised reaction solutions were further analysed by GC-MS according to the method shown below. A commercial sample of sodium lactate of natural isotopic abundance was derivatised and analysed in an identical manner for comparison. Conditions as below:
[0483] Column: DB-1701 (agilent), 30 m length, 0.25 mm diameter, 0.25 m (film thickness); Carrier: He (CP grade), 100 kPa (constant pressure); Inlet temperature: 250 C.; Injection conditions: Split (10:1) with split flow 12 mL/min, splitless time 0.7 mins, purge 5 mL/min; Detection: Mass Spec, EI (70 eV), source temperature 230 C. Scan range 50-650 amu with a scan rate of 5 Hz. Transfer line 300 C.; Oven heating profile:
TABLE-US-00009 Time (minutes) Temperature 0 .fwdarw. 5 Hold at 50 C. 5 .fwdarw. 16.3 Ramp to 275 C. at 20 C./min 16.3 .fwdarw. 18.8 Hold at 275 C. for 2.5 mins
[0484] .sup.1H NMR spectroscopy: After removal of the catalyst, the unmodified reaction solutions were analysed by .sup.1H NMR spectroscopy at 500 MHz and 298 K.
[0485] Results are shown in
[0486] The very high conversion of pyruvate to lactate was confirmed by GC-FID analysis of the derivatised reaction solution (see
Example 9.2
[0487] In this reaction phenylpyruvate was converted to [2,3-.sup.2H.sub.3]-L-phenylalanine. Phenylpyruvic acid (5 mM) in 0.5 mL of (.sup.2H.sub.11)-Tris-.sup.2HCl (100 mM, p.sup.2H 8.0) was first allowed to stand for 24 hours in order to exchange labile protons for deuterons, before the addition of 25 mM NH.sub.4Cl, 0.5 mM NAD.sup.+, and 500 g of L-phenylalanine dehydrogenase. The mixture was presaturated with H.sub.2 gas prior to addition of the Bio-catalyst systems at a loading of 400 g. The reaction was then shaken at 500 rpm under a steady flow of H.sub.2 for 16 hours.
[0488] GC-FID: In order to determine the conversion of phenylpyruvate to alanine, the analytes were first derivatised and then subjected to analysis by GC-FID. 100 L of reaction mixture was combined with 23 L of EtOH and 13 L of pyridine by means of a vortex mixer. Subsequently, 15 L of ethyl chloroformate was added, and the reaction allowed to proceed until no further CO.sub.2 was evolved. The derivatised pyruvate/alanine was extracted with 100 L of C.sup.2HCl.sub.3, and transferred to a glass vial for analysis by GC. Conditions as below:
[0489] Column: DB-1701 (Agilent), 30 m length, 0.25 mm diameter, 0.25 m film thickness; Carrier: He (CP grade), 170 kPa (constant pressure); Inlet temperature: 230 C.; Injection conditions: Splitless with split flow 50 mL/min, splitless time 0.7 mins, purge 5 mL/min; Injection volume: 0.5 L; Detection: FID;
[0490] Detector temperature: 250 C.; Detection gases: H.sub.2 (35 mL/min), air (350 mL/min), makeup N.sub.2 (40 mL/min); Oven heating profile:
TABLE-US-00010 Time (minutes) Temperature 0 .fwdarw. 5 Hold at 100 C. .sup.5 .fwdarw.30 Ramp to 150 C. at 2 C./min 30 .fwdarw. 35 Hold at 150 C. for 5 minutes .sup.35 .fwdarw. 41.5 Ramp to 280 C. at 2 C./min 41.5 .fwdarw. 46.5 Hold at 280 C. for 5 minutes
[0491] GC-MS: The N-ethoxycarbonyl ethylester-derivatised samples from the GC-FID analysis described (see above) were subsequently analysed by GC-MS according to the method below. A commercial sample of L-phenylalanine of natural isotopic abundance was derivatised and analysed in an identical manner for comparison. Conditions as below: Column: DB-1701 (agilent), 30 m length, 0.25 mm diameter, 0.25 m (film thickness); Carrier: He (CP grade), 100 kPa (constant pressure); Inlet temperature: 250 C.; Injection conditions: Split (10:1) with split flow 12 mL/min, splitless time 0.7 mins, purge 5 mL/min; Detection: Mass Spec, EI (70 eV), source temperature 230 C. Scan range 50-650 amu with a scan rate of 5 Hz. Transfer line 300 C.; Oven heating profile:
TABLE-US-00011 Time (minutes) Temperature 0 .fwdarw. 5 Hold at 50 C. 5 .fwdarw. 16.3 Ramp to 275 C. at 20 C./min 16.3 .fwdarw. 18.8 Hold at 275 C. for 2.5 mins
[0492] Chiral GC-FID: Derivatisation of the samples for analysis by chiral GC-FID to establish the enantiomeric excess of the reaction, was carried out as described above, except with nPrOH (30 L) substituted for EtOH. Chiral GC-FID was then carried out according to the following method. Conditions as below:
[0493] Column: CP-Chirasil-Dex CB (Agilent), 25 m length, 0.25 mm diameter, 0.25 m (film thickness), fitted with a guard of 10 m undeactivated fused silica of the same diameter; Carrier: He (CP grade), 2 mL/min (constant flow); Inlet temperature: 200 C.; Injection conditions: Splitless with split flow 80 mL/min, splitless time 0.8 mins, purge 5 mL/min.; Injection volume=0.3 L; Detection: FID; Detector temperature: 200 C.; Detection gases: H.sub.2 (35 mL/min), air (350 mL/min), makeup N.sub.2 (40 mL/min); Oven heating profile:
TABLE-US-00012 Time (minutes) Temperature 0 .fwdarw. 5 Hold at 70 C. 5 .fwdarw. 115 Ramp to 180 C. at 1 C./min 115 .fwdarw. 130 Hold at 180 C. for 15 minutes
[0494] .sup.1H NMR spectroscopy: After removal of the catalyst, the unmodified reaction solutions were analysed by .sup.1H NMR spectroscopy at 500 MHz and 298 K.
[0495] Results are shown in
[0496] The very high conversion of phenylpyruvate to phenylalanine was confirmed by GC-FID analysis of the derivatised reaction solution (see
Example 9.3
[0497] In this reaction cinnamaldehyde was selectively deuterated using alcohol dehydrogenase (reaction A), ene reductase (reaction B), or both ene reductase and subsequently alcohol dehydrogenase (reaction C).
[0498] Cinnamaldehyde was used as a substrate (bearing an alpha, beta-unsaturated aldehyde moiety) to investigate the chemoselectivity of the H.sub.2-driven labelling strategy. Conventional hydrogenation of this substrate typically results in a mixture of products (hydrocinnamaldehyde, cinnamyl alcohol and 3-phenyl-1-propanol) (56), however, by using either an ene reductase or an alcohol dehydrogenase alone, or the two enzymes in a step-wise one-pot reaction, the results below demonstrate that high chemical control over the deuterium-labelled product could be achieved.
[0499] Reactions were conducted in 0.5 mL of (.sup.2H.sub.11)-Tris-.sup.2HCl (100 mM, p.sup.2H 8.0) containing 5 mM cinnamaldehyde, 2 vol. % DMSO, 0.5 mM NAD.sup.+, and 500 g of (A) alcohol dehydrogenase (JM, ADH 105), and (B-C) ene reductase (JM, ENE101). The mixture was presaturated with H.sub.2 gas prior to addition of the heterogeneous biocatalytic system at a loading of 400 g. The reactions were shaken at 500 rpm under a steady flow of H.sub.2 for 16 hours. In the case of reaction C, the initial step was allowed to proceed for 24 hours before addition of a further 200 g of the heterogeneous biocatalytic system and 500 g of alcohol dehydrogenase (JM, ADH 105).
[0500] GC-FID: Following the reactions, an aliquot of the solution was extracted with a 2volume of C.sup.2HCl.sub.3, and then centrifuged at 18 800g for 5 minutes before being transferred to glass vials for analysis by GC-FID according to the method below. Column: DB-1701 (Agilent), 30 m length, 0.25 mm diameter, 0.25 m film thickness; Carrier: He (CP grade), 0.5 mL minute (constant flow); Inlet temperature: 230 C.; Injection conditions: Splitless with split flow 60 mL/min, splitless time 0.8 mins, purge 5 mL/min; Injection volume: 0.5 L; Detection: FID; Detector temperature: 150 C.; Detection gases: H.sub.2 (35 mL/min), air (350 mL/min), makeup N.sub.2 (40 mL/min); Oven heating profile:
TABLE-US-00013 Time (minutes) Temperature 0 .fwdarw. 5 Hold at 50 C. .sup.5 .fwdarw.25 Ramp to 250 C. at 10 C./min 25 .fwdarw. 35 Hold at 250 C. for 10 mins
[0501] GC-MS: Following extraction and analysis by GC-FID (above) the reaction solutions were analysed by GC-MS according to the method below. Column: DB-1701 (agilent), 30 m length, 0.25 mm diameter, 0.25 m (film thickness); Carrier: He (CP grade), 100 kPa (constant pressure); Inlet temperature: 250 C.; Injection conditions: Split (25:1) with split flow 30 mL/min, splitless time 0.7 mins, purge 5 mL/min; Detection: Mass Spec, EI (70 eV), source temperature 230 C. Scan range 50-650 amu with a scan rate of 5 Hz; Transfer line 300 C.; Oven heating profile:
TABLE-US-00014 Time (minutes) Temperature 0 .fwdarw. 5 Hold at 50 C. 5 .fwdarw. 16.3 Ramp to 275 C. at 20 C./min 16.3 .fwdarw. 18.8 Hold at 275 C. for 2.5 mins
[0502] .sup.1H NMR spectroscopy: After removal of the catalyst, the unmodified reaction solutions were analysed by .sup.1H NMR spectroscopy at 500 MHz and 298 K. In the case of reactions A and C, it was necessary to acquire additional spectra under non-aqueous conditions by extracting the product into an equal volume of C.sup.2HCl.sub.3 and re-analysing it.
[0503] The results for reactions A, B, and C are shown in
[0504] A: [1-.sup.2H]-Cinnamyl Alcohol
[0505] Analysis by GC-FID,
[0506] Accordingly, the peak corresponding to the neighbouring C2 proton is also found to change from a doublet of triplets in the unlabelled standard (=6.47 ppm, dt, J=16.1 Hz, J=5.8 Hz), to a doublet of doublets in the deuterated product (=6.47 ppm, dd, J=16.1 Hz, J=5.8 Hz). Unfortunately, mass spectroscopic analysis could not be used to unambiguously evaluate the extent of %.sup.2H labelling, as such compounds are known to re-arrange upon ionization, causing large differences in the fragmentation pattern of different isotopomers. However, the spectra were still acquired, and are shown in
[0507] B: [2, 3-.sup.2H.sub.2]-hydrocinnamaldehyde
[0508] The near quantitative conversion of cinnamaldehyde to hydorcinnamaldehyde could was demonstrated by GC-FID analysis, see
[0509] C: [1,2,3-.sup.2H.sub.3.5]-3-phenyl-1-propanol
[0510] The conversion of cinnamaldehyde to hydrocinnamaldehyde by the action of the heterogeneous biocatalytic system and an ene reductase was shown to proceed quantitiatively. The second half of Reaction C, in which the hydrocinnamaldehyde was reduced further to 3-phenyl-1-propanol by the introduction of an alcohol dehydrogenase, was shown to proceed to a similarly high degree by GC-FID analysis (see
Example 9.4
[0511] In this reaction carvones were selectively reduced to [1,2-.sup.2H.sub.2]-dihydrocarvones using ene reductase Reactions were conducted in 0.5 mL of (.sup.2H.sub.5)-Tris-.sup.2HCl (100 mM, p.sup.2H 8.0) containing 5 mM (4R)-carvone (Reaction A) or (4S)-carvone (Reaction B), 4 vol. % [.sup.2H.sub.6]-DMSO, 0.5 mM NAD.sup.+, and 500 g of ene reductase (JM, ENE101). The mixture was presaturated with H.sub.2 gas prior to addition of the heterogeneous bio-system at a loading of 400 g. The reactions were shaken at 500 rpm under a steady flow of H.sub.2 for 16 hours. Evaporation of the product dihydrocarvones proved to more problematic than in other cases so alternative reaction setups were trialled, including a pressure vessel (Bchi Tinyclave) sealed under 2 bar H.sub.2 (50 mL headspace), and a reaction in a 1.5 mL glass GC-vial sealed under H.sub.2 balloon pressure. Whilst a commercial standard of mixed of (1R, 4R)- and (1S, 4R)-dihydrocarvone was commercially available, the 4S-epimer was unavailable. Instead, this was synthesised by reduction of (4S)-carvone by Zn metal. Here, Zn metal (625 mg, 9.6 mmol) and KOH (250 mg, 4.5 mmol) were combined in 3.5 mL of MeOH/H.sub.2O (95/5 v/v) and the slurry bought to reflux under stirring. (4S)-carvone (500 mg, 3.3 mmol) was dissolved in 1 mL of MeOH/H.sub.2O (95/5 v/v) and added dropwise to the Zn-solution over 6 hours. Following the reaction, the solution was filtered through a syringe filter, extracted into pentane (31 mL) and dried over Na.sub.2SO.sub.4. The solvent was removed in vacuo to give (4S)-dihydrocarvone (400 mg, 80%) as a mixture of cis-1,4 and trans-1,4 epimers in the ratio 83:17 (by GC). In order to assist in the assignment of the .sup.1H NMR spectra of the deuterated samples, (1R, 4R)- and (1R, 4S)-dihydrocarvones of natural isotopic abundance were also prepared at high de from their parent (4R)- and (4S)-carvones by reaction with an ene reductase. Here, the relevant carvone (5 mM) was shaken with 500 g of ene reductase (JM, ENE101) in 500 L of non-deuterated Tris buffer (100 mM, pH 8.0) containing 2 vol. % DMSO and 10 mM NADH for 6 hours at room temperature. .sup.2H.sub.2O (100 L) was added to the sample for field locking purposes, and the reaction mixture was analysed immediately by .sup.1H NMR spectroscopy.
[0512] GC-FID: Following the reactions, an aliquot of the solution was extracted with a 2volume of C.sup.2HCl.sub.3, and then centrifuged at 18 800g for 5 minutes before being transferred to glass vials for analysis by GC-FID according to the method below. Column: DB-1701 (Agilent), 30 m length, 0.25 mm diameter, 0.25 m film thickness; Carrier: He (CP grade), 0.5 mL minute (constant flow); Inlet temperature: 230 C.; Injection conditions: Splitless with split flow 60 mL/min, splitless time 0.8 mins, purge 5 mL/min.; Injection volume: 0.5 L; Detection: FID; Detector temperature: 150 C.; Detection gases: H.sub.2 (35 mL/min), air (350 mL/min), makeup N.sub.2 (40 mL/min); Oven heating profile:
TABLE-US-00015 Time (minutes) Temperature 0 .fwdarw. 5 Hold at 50 C. .sup.5 .fwdarw.25 Ramp to 250 C. at 10 C./min 25 .fwdarw. 35 Hold at 250 C. for 10 mins
[0513] GC-MS: Following extraction and analysis by GC-FID (above) the reaction solutions were analysed by GC-MS according to the method below. Column: DB-1701 (agilent), 30 m length, 0.25 mm diameter, 0.25 m (film thickness); Carrier: He (CP grade), 100 kPa (constant pressure); Inlet temperature: 250 C.; Injection conditions: Split (10:1) with split flow 12 mL/min, splitless time 0.7 mins, purge 5 mL/min; Detection: Mass Spec, EI (70 eV), source temperature 230 C. Scan range 50-650 amu with a scan rate of 5 Hz. Transfer line 300 C.; Oven heating profile:
TABLE-US-00016 Time (minutes) Temperature 0 .fwdarw. 5 Hold at 50 C. 5 .fwdarw. 16.3 Ramp to 275 C. at 20 C./min 16.3 .fwdarw. 18.8 Hold at 275 C. for 2.5 mins
[0514] .sup.1H NMR spectroscopy: After removal of the catalyst, the unmodified reaction solutions were analysed by .sup.1H NMR spectroscopy at 500 MHz and 298 K. In order to confirm assignments, .sup.1H-.sup.1H correlation spectroscopy (COSY) was also conducted on the samples as required.
[0515] Results are shown in
[0516] A: [1, 2-.sup.2H.sub.2]-(1R, 4R)-dihydrocarvone
[0517] Analysis by GC-FID confirmed the high conversion of substrate to product, and the high selectivity for the trans-1,4 diastereomer (see
[0518] B: [1, 2-.sup.2H.sub.2]-(1R, 4S)-dihydrocarvone
[0519] Analysis by GC-FID yielded results that were similar to those for Reaction A described above. Again, conversion from (4S)-carvone to (1R, 4S)-dihydrocarvone was found to be virtually quantitative (see
Example 10
[0520] This Example demonstrates the method of the invention in selective tritiation, wherein x=3 for the source of the isotopic label .sup.xH.sub.2O (i.e. .sup.3H.sub.2O).
[0521] .sup.3H.sub.2O from PerkinElmer (500 L, pH 8.0, diluted with .sup.1H.sub.2O to an activity of 18.5 MBq; i.e. around 0.3 ppm .sup.3H in the .sup.3H.sub.2O/.sup.1H.sub.2O mixture) containing Tris.HCl (100 mM) and NAD.sup.+ (5 mM) was sealed in a conical glass flask with a Suba-Seal, and sparged with gaseous N.sub.2 and then gaseous H.sub.2 for 30 minutes each. 5 L of R. eutropha soluble hydrogenase (SEQ ID NOs: 1, 2, 3, 30, 31) was added, and the reaction mixture was allowed to stand at room temperature under a balloon pressure of H.sub.2 gas for 16 hours. A UV torch (=360 nm) was used to confirm that NADH was been formed under these conditions.
[0522] To confirm that the formed NADH was labelled with .sup.3H at the 4-position, a subsequent experiment was setup with the same .sup.3H.sub.2O solution and 0.5 mM NAD.sup.+. To this second solution was added 10 mM acetophenone, 2 vol. % of DMSO and 0.5 mg of R-selective alcohol dehydrogenase (ADH101). 5 L of R. eutropha soluble hydrogenase (SEQ ID NOs: 1, 2, 3, 30, 31) was added, and the reaction mixture was allowed to stand at room temperature under a balloon pressure of H2 gas for 16 hours. The (R)-phenylethanol product was extracted into 1 mL of C.sup.2HCl.sub.3, and dried with 150 mg of anhydrous P.sub.2O.sub.5 to remove residual H.sub.2O.
[0523] Product analysis was conducted by .sup.1H NMR spectroscopy in the manner detailed above, and confirmed a conversion of >80% to the 1-phenylethanol product (see
[0524] To establish the extent of .sup.3H radiolabelling on the product, liquid scintillation counting (LSC) of the C.sup.2HCl.sub.3 extract was conducted as follows: LSC was carried out on a Beckman LS6500 machine, using 500 L of analyte solution and 5 mL of PerkinElmer Ultima Gold LLT scintillant. A calibration was conducted to establish the LSC response for a known quantity of .sup.3H using measured amounts of [.sup.3H]-toluene (PerkinElmer LSC standard, 43.3 kBq/g) dissolved in 500 uL of C.sup.2HCl.sub.3. A counting time of 1 minute was used at each concentration, and an exemplar plot is shown in
[0525] This experiment thus confirms that H.sub.2-driven NADH recycling may be driven in .sup.3H.sub.2O to deliver a [.sup.3H]-labelled product.
ASPECTS OF THE INVENTION
[0526] 1. A method of producing a reduced labelled cofactor comprising one or more .sup.xH atom, wherein x is 2 or 3, wherein said method comprises: [0527] i) providing a composition comprising (i) .sup.xH.sup.+ ions and (ii) an oxidised cofactor; [0528] ii) transferring electrons from an electron source to a first polypeptide which is an NADH:acceptor oxidoreductase or an NADPH:acceptor oxidoreductase or a functional derivative or fragment thereof; and [0529] iii) contacting the .sup.xH.sup.+ ions and the oxidised cofactor with the first polypeptide thereby reducing the oxidised cofactor to form a reduced labelled cofactor comprising one or more .sup.xH atoms. [0530] 2. A method according to aspect 1, wherein said method is a method of producing a reduced labelled reaction product comprising one or more .sup.xH atom, wherein x is 2 or 3, wherein said method comprises producing a reduced labelled cofactor according to aspect 1; and [0531] iv) contacting the reduced labelled cofactor and an oxidised reactant with at least one enzyme that is an NADH-dependent oxidoreductase or an NADPH-dependent oxidoreductase or a functional derivative or fragment thereof such that the enzyme selectively transfers an .sup.xH atom from the reduced labelled cofactor to the oxidised reactant thereby producing a reduced labelled reaction product and an oxidised cofactor. [0532] 3. A method according to aspect 2 which further comprises reducing the oxidised cofactor produced in step (iv) of aspect 2 in a method according to aspect 1. [0533] 4. A method according to aspect 2 which comprises producing a reduced labelled reaction product according to steps (i) to (iv) of aspects 1 and 2, and repeating steps (ii) to (iv) multiple times, thereby recycling the cofactor. [0534] 5. A method according to any one of the preceding aspects wherein the .sup.xH.sup.+ ions are provided as .sup.2H.sub.2O or .sup.3H.sub.2O. [0535] 6. A method according to any one of the preceding aspects wherein: [0536] (i) the oxidised cofactor is NAD.sup.+, NADP.sup.+, or a labelled version of NAD.sup.+ or NADP.sup.+ comprising at least one .sup.xH atom, wherein preferably reducing the oxidised cofactor to form a reduced labelled cofactor comprises adding an .sup.xH atom at the 4-position of the nicotinamide ring of the oxidised cofactor; and/or [0537] (ii) the .sup.xH.sup.+ ions are transferred directly from the composition comprising .sup.xH.sup.+ ions to the first polypeptide. [0538] 7. A method according to any one of the preceding aspects wherein the first polypeptide transfers an .sup.xH.sup. anion to the oxidised cofactor thereby forming the reduced labelled cofactor, wherein preferably: [0539] A. the first polypeptide comprises a flavin group; and/or [0540] B. the first polypeptide has a structure comprising a Rossmann fold; and/or [0541] C. the first polypeptide comprises or consists of a diaphorase moiety; and/or [0542] D. the first polypeptide consists or comprises of one or more than one of: [0543] i) the amino acid sequence of Ralstonia eutropha diaphorase HoxF (SEQ ID NO: 1) or an amino acid sequence having at least 60% homology therewith; [0544] ii) the amino acid sequence of Ralstonia eutropha diaphorase HoxU (SEQ ID NO: 2) or an amino acid sequence having at least 60% homology therewith; [0545] iii) the amino acid sequence of Ralstonia eutropha diaphorase HoxI (SEQ ID NO: 3) or an amino acid sequence having at least 60% homology therewith; [0546] iv) the amino acid sequence of the 51 kDa protein of the flavoprotein (Fp) subcomplex of Complex I of Bos taurus (SEQ ID NO: 4) or an amino acid sequence having at least 60% homology therewith; [0547] v) the amino acid sequence of the 24 kDa subcomplex of Complex I of Bos taurus (SEQ ID NO: 5) or an amino acid sequence having at least 60% homology therewith; [0548] vi) the amino acid sequence of Ralstonia eutropha NAD.sup.+-dependent formate dehydrogenase diaphorase moiety FdsB (SEQ ID NO: 6) or an amino acid sequence having at least 60% homology therewith; [0549] vii) the amino acid sequence of Ralstonia eutropha NAD.sup.+-dependent formate dehydrogenase diaphorase moiety FdsG (SEQ ID NO: 7) or an amino acid sequence having at least 60% homology therewith; [0550] viii) the amino acid sequence of Rhodobacter capsulatus NAD.sup.+-dependent formate dehydrogenase, diaphorase moiety FdsB (SEQ ID NO: 8) or an amino acid sequence having at least 60% homology therewith; [0551] ix) the amino acid sequence of Rhodobacter capsulatus NAD.sup.+-dependent formate dehydrogenase, diaphorase moiety FdsG (SEQ ID NO: 9) or an amino acid sequence having at least 60% homology therewith; [0552] x) the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase I gamma subunit (SEQ ID NO: 10) or an amino acid sequence having at least 60% homology therewith; [0553] xi) the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase I beta subunit (SEQ ID NO: 11) or an amino acid sequence having at least 60% homology therewith; [0554] xii) the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase II gamma subunit (SEQ ID NO: 12) or an amino acid sequence having at least 60% homology therewith; [0555] xiii) the amino acid sequence of the amino acid sequence of the NADPH oxidoreductase moiety from Pyrococcus furiosus soluble hydrogenase II beta subunit (SEQ ID NO: 13) or an amino acid sequence having at least 60% homology therewith; [0556] xiv) the amino acid sequence of the diaphorase moiety of Rhodococcus opacus soluble hydrogenase HoxF (SEQ ID NO: 14) or an amino acid sequence having at least 60% homology therewith; [0557] xv) the amino acid sequence of the diaphorase moiety of Rhodococcus opacus soluble hydrogenase HoxU (SEQ ID NO: 15) or an amino acid sequence having at least 60% homology therewith; [0558] xvi) the amino acid sequence of the diaphorase moiety of Allochromatium vinosum soluble hydrogenase HoxF (SEQ ID NO: 16) or an amino acid sequence having at least 60% homology therewith; [0559] xvii) the amino acid sequence of the diaphorase moiety of Allochromatium vinosum soluble hydrogenase HoxU (SEQ ID NO: 17) or an amino acid sequence having at least 60% homology therewith; [0560] xviii) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina Hox1F (SEQ ID NO: 18) or an amino acid sequence having at least 60% homology therewith; [0561] xix) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina soluble hydrogenase Hox1U (SEQ ID NO: 19) or an amino acid sequence having at least 60% homology therewith; [0562] xx) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina Hox2F (SEQ ID NO: 20) or an amino acid sequence having at least 60% homology therewith; [0563] xxi) the amino acid sequence of the diaphorase moiety of Thiocapsa roseopersicina soluble hydrogenase Hox2U (SEQ ID NO: 21) or an amino acid sequence having at least 60% homology therewith; [0564] xxii) the amino acid sequence of the diaphorase moiety of Synechocystis sp. PCC 6803 HoxF (SEQ ID NO: 22) or an amino acid sequence having at least 60% homology therewith; [0565] xxiii) the amino acid sequence of the diaphorase moiety of Synechocystis sp. PCC 6803 HoxU (SEQ ID NO: 23) or an amino acid sequence having at least 60% homology therewith; [0566] xxiv) the amino acid sequence of the diaphorase moiety of Synechococcus elongatus PCC 6301 HoxF (SEQ ID NO: 24) or an amino acid sequence having at least 60% homology therewith; [0567] xxv) the amino acid sequence of the diaphorase moiety of Synechococcus elongatus PCC 6301 HoxU (SEQ ID NO: 25) or an amino acid sequence having at least 60% homology therewith; [0568] xxvi) the amino acid sequence of Hydrogenophilus thermoluteolus diaphorase HoxF (SEQ ID NO: 26) or an amino acid sequence having at least 60% homology therewith; [0569] xxvii) the amino acid sequence of Hydrogenophilus thermoluteolus diaphorase HoxU (SEQ ID NO: 27) or an amino acid sequence having at least 60% homology therewith; [0570] xxviii) the amino acid sequence of Chlamydomonas reinhardtii Ferredoxin-NADP+ reductase (SEQ ID NO: 28) or an amino acid sequence having at least 60% homology therewith; [0571] xxix) the amino acid sequence of Anabaena Ferredoxin-NADP+ reductase (SEQ ID NO: 29) or an amino acid sequence having at least 60% homology therewith; [0572] xxx) the amino acid sequence of Ralstonia eutropha diaphorase HoxF (SEQ ID NO: 70) or an amino acid sequence having at least 60% homology therewith; [0573] xxxi) the amino acid sequence of Ralstonia eutropha diaphorase with inactive hydrogenase (SEQ ID NO: 1 and/or 2 and/or 69 and/or 31) or an amino acid sequence having at least 60% homology therewith [0574] or a functional fragment, derivative or variant thereof; wherein more preferably the first polypeptide consists or comprises of the Ralstonia eutropha NAD.sup.+-reducing soluble hydrogenase or a functional fragment, derivative or variant thereof. [0575] 8. A method according to any one of the preceding aspects wherein the electron source comprises a second polypeptide which is an oxidising enzyme or functional derivative or fragment thereof capable of oxidising a reductant to extract electrons, wherein the second polypeptide transfers electrons from the reductant to the first polypeptide via an electronically-conducting pathway, wherein preferably (i) electrons are directly transferred along the electronically-conducting pathway or (ii) electron transfer along the electronically-conducting pathway is mediated by one or more electron mediators; wherein more preferably: [0576] A. the first polypeptide and the second polypeptide constitute component parts of a modular, multidomain or multicomponent protein or protein complex; and/or [0577] B. the second polypeptide is selected or modified to oxidise H.sub.2 or .sup.xH.sub.2 under the conditions of the method; and/or [0578] C. the second polypeptide is a hydrogenase enzyme or a functional derivative or fragment thereof, wherein preferably the hydrogenase is selected from [0579] i) the amino acid sequence of Ralstonia eutropha soluble hydrogenase moiety (SEQ ID NOs: 30 and/or 31) or an amino acid sequence having at least 60% homology therewith; [0580] ii) the amino acid sequence of Ralstonia eutropha membrane-bound hydrogenase moiety (SEQ ID NOs: 32 and/or 33 and/or 34) or an amino acid sequence having at least 60% homology therewith; [0581] iii) the amino acid sequence of Ralstonia eutropha regulatory hydrogenase moiety (SEQ ID NOs: 35 and/or 36) or an amino acid sequence having at least 60% homology therewith; [0582] iv) the amino acid sequence of Escherichia coli hydrogenase 1 (SEQ ID NOs:37 and/or 38) or an amino acid sequence having at least 60% homology therewith; [0583] v) the amino acid sequence of Escherichia coli hydrogenase 2 (SEQ ID NOs:39 and/or 40) or an amino acid sequence having at least 60% homology therewith; [0584] vi) the amino acid sequence of Aquifex aeolicus hydrogenase 1 (SEQ ID NO:41 and/or 42) or an amino acid sequence having at least 60% homology therewith; [0585] vii) the amino acid sequence of Hydrogenovibrio marinus hydrogenase (SEQ ID NOs: 43 and/or 44) or an amino acid sequence having at least 60% homology therewith; [0586] viii) the amino acid sequence of Thiocapsa roseopersicina hydrogenase (SEQ ID NOs: 45 and 46) or an amino acid sequence having at least 60% homology therewith; [0587] ix) the amino acid sequence of Alteromonas macleodii hydrogenase (SEQ ID NOs: 47 and/or 48) or an amino acid sequence having at least 60% homology therewith; [0588] x) the amino acid sequence of Rhodococcus opacus soluble hydrogenase moiety (SEQ ID NOs: 49 and/or 50) or an amino acid sequence having at least 60% homology therewith; [0589] xi) the amino acid sequence of Allochromatium vinosum membrane bound hydrogenase (SEQ ID NOs: 51 and/or 52) or an amino acid sequence having at least 60% homology therewith; [0590] xii) the amino acid sequence of Desulfovibrio fructosovorans membrane bound hydrogenase (SEQ ID NOs: 53 and/or 54) or an amino acid sequence having at least 60% homology therewith; [0591] xiii) the amino acid sequence of Clostridium pasteurianum iron-iron hydrogenase (SEQ ID NOs: 55) or an amino acid sequence having at least 60% homology therewith; [0592] xiv) the amino acid sequence of Clostridium acetobutylicum iron-iron hydrogenase (SEQ ID NOs: 56) or an amino acid sequence having at least 60% homology therewith; [0593] xv) the amino acid sequence of Chlamydomonas reinhardtii iron-iron hydrogenase (SEQ ID NOs: 57) or an amino acid sequence having at least 60% homology therewith; [0594] xvi) the amino acid sequence of Desulfomicrobium baculatum nickel-iron selenium hydrogenase (SEQ ID NOs: 58 and/or 59) or an amino acid sequence having at least 60% homology therewith; [0595] xvii) the amino acid sequence of Hydrogenophilus thermoluteolus soluble hydrogenase moiety (SEQ ID NOs: 60 and/or 61) or an amino acid sequence having at least 60% homology therewith; [0596] xviii) the amino acid sequence of Desulfovibrio vulgaris Nickel Iron hydrogenase (pdb 1H.sub.2A) (SEQ ID NOs: 62 and/or 63) or an amino acid sequence having at least 60% homology therewith; [0597] xix) the amino acid sequence of Desulfovibrio gigas Periplasmic [NiFe] hydrogenase (SEQ ID NOs: 64 and/or 65) or an amino acid sequence having at least 60% homology therewith; [0598] xx) the amino acid sequence of Salmonella enterica serovar Typhimurium LT2 nickel-iron hydrogenase 5 (SEQ ID NO: 66 and/or 67) or an amino acid sequence having at least 60% homology therewith. [0599] xxi) the amino acid sequence of Pyrococcus furiosus soluble alpha subunit (SEQ ID NOs: 68) or an amino acid sequence having at least 60% homology therewith; [0600] or a functional fragment, derivative or variant thereof. [0601] 9. A method according to any one of aspects 1 to 7 wherein [0602] i) the electron source comprises a synthetic organic, inorganic or metallic oxidation catalyst capable of oxidising a reductant to extract electrons, wherein the oxidation catalyst transfers electrons from the reductant to the first polypeptide via an electronically-conducting pathway; wherein preferably the oxidation catalyst comprises platinum, palladium, iridium nickel, rhodium and/or ruthenium; or [0603] ii) the electron source comprises an electrode connected to an electrode controller, wherein the electrode is connected to the first polypeptide via an electronically-conducting pathway. [0604] 10. A method according to aspects 8 or 9 wherein the reductant oxidised by the second polypeptide or the oxidation catalyst is H.sub.2 or .sup.xH.sub.2, preferably H.sub.2. [0605] 11. A method according to any one of aspects 8 to 10 wherein the electron source comprises a second polypeptide as defined in aspect 8 or an oxidation catalyst as defined in aspect 9, and wherein the electron source and the first polypeptide are each in electronic contact with an electronically conducting support, wherein preferably: [0606] a. the electron source and the first polypeptide are each in electronic contact with the same electronically conducting support, wherein preferably the support is an electronically conducting particle; or [0607] b. the electron source is in electronic contact with an electronically conducting first support and the first polypeptide is in electronic contact with an electronically conducting second support; and the first support is in electronic contact with the second support. [0608] 12. A method according to aspect 11 wherein the or each support comprises a material comprising carbon, a metal or metal alloy, a metal oxide or mixed metal oxide, a metal hydroxide, a metal chalcogenide, a semi-conducting material, or an electronically-conductive polymer, or mixtures thereof; or according to aspect 9 wherein the electron source comprises an electrode connected to an electrode controller and the electrode comprises a material comprising carbon, a metal or metal alloy, a metal oxide or mixed metal oxide, a metal hydroxide, a metal chalcogenide, or an electronically-conductive polymer, or mixtures thereof; [0609] wherein preferably the material comprises: [0610] i) Carbon, preferably graphite, carbon nanotube(s), carbon black, activated carbon, carbon nanopowder, vitreous carbon, carbon fibre(s), carbon cloth, carbon felt, carbon paper, graphene, highly oriented pyrolytic graphite, pyrolytic graphite, or doped diamond; and/or [0611] ii) a metal or metal alloy selected from gold, silver, tungsten, iridium, platinum, palladium, copper, titanium, brass, and steel; and/or [0612] iii) a material selected from titanium oxide, indium oxide, tin oxide and indium tin oxide; [0613] 13. A method according to any one of aspects 2 to 12 wherein the at least one enzyme that is an NADH-dependent oxidoreductase or NADPH-dependent oxidoreductase is at least one of an NAD(P)H-dependent alcohol dehydrogenase, an NAD(P)H-dependent ene reductase, an NAD(P)H-dependent imine reductase or an NAD(P)H-dependent amino-acid dehydrogenase, wherein preferably the at least one enzyme that is an NADH-dependent oxidoreductase or NADPH-dependent oxidoreductase is at least one of an alcohol dehydrogenase or an amino acid dehydrogenase. [0614] 14. A system for performing a method according to any one of aspects 1 to 13, the system comprising: [0615] i) a composition comprising (i) .sup.xH.sup.+ ions wherein x is 2 or 3 and (ii) an oxidised cofactor, wherein preferably the composition is as defined in aspect 5 and/or the oxidised cofactor is as defined in aspect 6; [0616] ii) an electron source, wherein preferably the electron source is as defined in any one of aspects 8 to 12; and [0617] iii) a first polypeptide which is an NADH:acceptor oxidoreductase or an NADPH:acceptor oxidoreductase or a functional derivative or fragment thereof, wherein preferably the first polypeptide is as defined in any one of aspects 7; [0618] wherein the system is configured such that, in use, (a) electrons are transferred from the electron source to the first polypeptide and (b) .sup.xH.sup.+ ions and the oxidised cofactor are contacted with the first polypeptide so as to reduce the oxidised cofactor to form a reduced labelled cofactor comprising one or more .sup.xH atoms. [0619] 15. A method for producing an oxidised labelled cofactor comprising one or more .sup.xH atom, wherein x is 2 or 3, comprising producing a reduced labelled cofactor comprising one or more .sup.xH atom according to any one of aspects 1 to 13; and oxidising the reduced labelled cofactor.