Materials and methods for the biosynthesis of seven carbon chemicals in the presence of methanol oxidation
11492626 · 2022-11-08
Assignee
Inventors
- Alex Van Eck Conradie (Eaglescliffe, GB)
- Achuthanunni Chokkathukalam (Marske by the Sea, GB)
- Remi Ako Mbianyor Momo (Wilmington, DE, US)
Cpc classification
C12P13/005
CHEMISTRY; METALLURGY
C12P7/40
CHEMISTRY; METALLURGY
C12Y101/01284
CHEMISTRY; METALLURGY
C12Y301/02012
CHEMISTRY; METALLURGY
C12P13/00
CHEMISTRY; METALLURGY
International classification
C12P7/40
CHEMISTRY; METALLURGY
C12P13/00
CHEMISTRY; METALLURGY
C12N9/00
CHEMISTRY; METALLURGY
Abstract
This disclosure describes methods for regulating the biosynthesis of pimelic acid, 7-aminoheptanoate, 7-hydroxyheptanoate, heptamethylenediamine, 7-aminoheptanol, or 1,7-heptanediol by channeling increased flux through the biosynthesis pathway to obtain an intermediate required for growth of the host microorganism.
Claims
1. A method for regulating biosynthesis of a product in a host cell, wherein the product comprises pimelic acid, 7-aminoheptanoate, 7-hydroxyheptanoate, heptamethylenediamine, 7-aminoheptanol, or 1,7-heptanediol, or salts thereof, using a pathway having a pimeloyl-acyl carrier protein (pimeloyl-ACP) intermediate, the method comprising converting methanol to formate via enzymatic reaction, wherein the formate is used in the conversion of tetrahydrofolate to N1°-formyl-tetrahydrofolate, wherein: the methanol is produced during pimeloyl-ACP methyl ester esterase (BioH) enzyme activity in which BioH removes a methyl group from pimeloyl-ACP methyl ester during conversion of pimeloyl-ACP methyl ester to pimeloyl ACP, wherein the BioH activity is increased compared to an unmodified host cell: and the method comprises downregulating (a) bifunctional protein (FolD) activity by attenuating folD and/or (b) formate acetyltransferase 1 (PflB) activity and formate acetyltransferase-like enzyme (TdcE) activity: and the method comprises inserting into the host cell (i) a gene encoding an S-formylglutathione hydrolase (frmB), (ii) a gene encoding a formate-tetrahydrofolate ligase (fhs), (iii) a gene encoding an alcohol dehydrogenase (adh), and (iv) a gene encoding an S-(hydroxymethyl) glutathione dehydrogenase (frmA), wherein the S-formylglutathione hydrolase has at least 90% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 27-30, the formate-tetrahydrofolate ligase has at least 90% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 18-22, the alcohol dehydrogenase has at least 90% sequence identity to the amino acid sequence set forth in SEQ ID NO: 31, and the S-(hydroxymethyl) glutathione dehydrogenase has at least 90% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 23-26.
2. The method of claim 1, wherein: downregulating the activity of PflB and TdcE comprises a step of deleting pflB and tdcE.
3. The method of claim 1, wherein: the expression of adh, frmA, and frmB allows conversion of the methanol to formate; and the biosynthesis of the product is increased compared to a control cell transformed with a vector without said genes.
4. The method of claim 1, wherein the product comprises a salt of pimelic acid, 7-aminoheptanoate, 7-hydroxyheptanoate, heptamethylenediamine, 7-aminoheptanol, or 1,7-heptanediol.
5. The method of claim 1, wherein the method is performed in a recombinant host.
6. The method of claim 5, wherein a principal carbon source fed to the host derives from biological or non-biological feedstocks.
7. The method of claim 6, wherein: the biological feedstock is, or derives from, monosaccharides, disaccharides, lignocellulose, hemicellulose, cellulose, lignin, levulinic acid, formic acid, triglycerides, glycerol, fatty acids, agricultural waste, condensed distillers' solubles, or municipal waste: or the non-biological feedstock is, or derives from, natural gas, syngas, CO.sub.2/H.sub.2, methanol, ethanol, benzoate, non-volatile residue (NVR) caustic wash waste stream from cyclohexane oxidation processes, or terephthalic acid/isophthalic acid mixture waste streams.
8. The method of claim 5, wherein the host is a prokaryote selected from the group consisting of the following genera: Escherichia; Clostridia; Corynebacteria; Cupriavidus; Pseudomonas; Delftia; Bacillus; Lactobacillus; Lactococcus; and Rhodococcus; or the host is a eukaryote selected from the group consisting of the following genera: Aspergillus; Saccharomyces; Pichia; Yarrowia; Issatchenkia; Debaryomyces; Arxula; and Kluyveromyces.
9. The method of claim 8, wherein the host is Escherichia coli.
10. The method of claim 8, wherein: the prokaryote is Escherichia coli, Clostridium lungdahlii, Clostridium autoethanogenum, Clostridium kluyveri, Corynebacterium glutamicum, Cupriavidus necator, Cupriavidus metallidurans, Pseudomonas fluorescens, Pseudomonas putida, Pseudomonas oleavorans, Delftia acidovorans, Bacillus subtillis, Lactobacillus delbrueckii, Lactococcus lactis, or Rhodococcus equi; or the eukaryote is Aspergillus niger, Saccharomyces cerevisiae, Pichia pastoris, Yarrowia lipolytica, Jssathenkia orientalis, Debaryomyces hansenii, Arxula adenoinivorans, or Kluyveromyces lactis.
11. The method of claim 5 wherein: the host comprises one or more of the following attenuated enzymes: polyhydroxyalkanoate synthase; an acetyl-CoA thioesterase; an acetyl-CoA specific β-ketothiolase; a phosphotransacetylase forming acetate; an acetate kinase; a lactate dehydrogenase; a menaquinol-fumarate oxidoreductase; a 2-oxoacid decarboxylase producing isobutanol; an alcohol dehydrogenase forming ethanol; a triose phosphate isomerase; a pyruvate decarboxylase; a glucose-6-phosphate isomerase; a transhydrogenase dissipating the NADH or NADPH imbalance; a glutamate dehydrogenase dissipating the NADH or NADPH imbalance; a NADH/NADPH-utilizing glutamate dehydrogenase; a pimeloyl-CoA dehydrogenase; an acyl-CoA dehydrogenase accepting C7 building blocks and central precursors as substrates; a glutaryl-CoA dehydrogenase; or a pimeloyl-CoA synthetase; and/or the host overexpresses an acetyl-CoA synthetase; a 6-phosphogluconate dehydrogenase; a transketolase; a puridine nucleotide transhydrogenase; a formate dehydrogenase; a glyceraldehyde-3P-dehydrogenase; a malic enzyme; a glucose-6-phosphate dehydrogenase; a fructose 1,6 diphosphatase; a L-alanine dehydrogenase; a L-glutamate dehydrogenase specific to the NADH or NADPH used to generate a co-factor imbalance; a methanol dehydrogenase; a formaldehyde dehydrogenase; a diamine transporter; a dicarboxylate transporter; an S-adenosylmethionine synthetase; and/or a multidrug transporter.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION
(16) The following detailed description and examples illustrate certain embodiments of the present disclosure. Those of skill in the art will recognize that there are numerous variations and modifications of this disclosure that are encompassed by its scope. Accordingly, the description of certain embodiments should not be deemed as limiting.
(17) Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. Although methods and materials similar or equivalent to those described herein can be used to practice the invention, suitable methods and materials are described below. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.
(18) This disclosure provides enzymes, non-natural pathways, cultivation strategies, feedstocks, host microorganisms and attenuations to the host's biochemical network, which generates a seven carbon chain aliphatic backbone from central precursors in which two terminal functional groups may be formed leading to the synthesis of pimelic acid, 7-aminoheptanoic acid (7-AHA), heptamethylenediamine or 1,7-heptanediol (referred to as “C7 building blocks” herein). As used herein, the term “central precursor” is used to denote any precursor or metabolite leading to the synthesis of a final product, such as, for example, a c C7 building block.The term “central metabolite” is used herein to denote a metabolite that is produced in all microorganisms to support growth.
(19) The reactions of the pathways described herein can be performed in one or more cell (e.g., host cell) strains (a) naturally expressing one or more relevant enzymes, (b) genetically engineered to express one or more relevant enzymes, or (c) naturally expressing one or more relevant enzymes and genetically engineered to express one or more relevant enzymes. Alternatively, relevant enzymes can be extracted from any of the above types of host cells and used in a purified or semi-purified form. Extracted enzymes can optionally be immobilized to a solid substrate such as the floors and/or walls of appropriate reaction vessels. Moreover, such extracts include lysates (e.g., cell lysates) that can be used as sources of relevant enzymes. In the methods provided by the disclosure, all the steps can be performed in cells (e.g., host cells), all the steps can be performed using extracted enzymes, or some of the steps can be performed in cells and others can be performed using extracted enzymes.
(20) Host microorganisms described herein can include endogenous pathways that can be manipulated such that one or more C7 building blocks can be produced. Host microorganisms can also include endogenous pathways that can be manipulated to regulate the biosynthesis of one or more C7 building blocks. In an endogenous pathway, the host microorganism naturally expresses all of the enzymes catalyzing the reactions within the pathway. A host microorganism containing an engineered pathway does not naturally express all of the enzymes catalyzing the reactions within the pathway but has been engineered such that all of the enzymes within the pathway are expressed in the host.
(21) As used herein, a “bio-based product” is a product in which both the feedstock (e.g., sugars from sugar cane, corn, wood; biomass; waste streams from agricultural processes) and the conversion process to the product are biologically based (e.g., fermentation/enzymatic transformation involving a biological host/organism/enzyme). As used herein, a “bio-derived product” is a product in which one of the feedstocks (e.g., sugars from sugar cane, corn, wood; biomass; waste streams from agricultural processes) or the conversion process to the product is biologically based (e.g., fermentation/enzymatic transformation involving a biological host/organism/enzyme).
(22) As used herein, a “fermentation-derived product” is a product produced by fermentation involving a biological host or organism.
(23) The term “C7 building block” is used to denote a seven (7) carbon chain aliphatic backbone.
(24) The term “exogenous” as used herein with reference to a nucleic acid (or a protein) and a host refers to a nucleic acid that does not occur in (and cannot be obtained from) a cell of that particular type as it is found in nature or a protein encoded by such a nucleic acid. Thus, a non-naturally-occurring nucleic acid is considered to be exogenous to a host once in the host. It is important to note that non-naturally-occurring nucleic acids can contain nucleic acid subsequences or fragments of nucleic acid sequences that are found in nature provided the nucleic acid as a whole does not exist in nature. For example, a nucleic acid molecule containing a genomic DNA sequence within an expression vector is non-naturally-occurring nucleic acid, and thus is exogenous to a host cell once introduced into the host, since that nucleic acid molecule as a whole (genomic DNA plus vector DNA) does not exist in nature. Thus, any vector, autonomously replicating plasmid, or virus (e.g., retrovirus, adenovirus, or herpes virus) that as a whole does not exist in nature is considered to be non-naturally-occurring nucleic acid. It follows that genomic DNA fragments produced by PCR or restriction endonuclease treatment as well as cDNAs are considered to be non-naturally-occurring nucleic acid since they exist as separate molecules not found in nature. It also follows that any nucleic acid containing a promoter sequence and polypeptide-encoding sequence (e.g., cDNA or genomic DNA) in an arrangement not found in nature is non-naturally-occurring nucleic acid. A nucleic acid that is naturally-occurring can be exogenous to a particular host microorganism. For example, an entire chromosome isolated from a cell of yeast x is an exogenous nucleic acid with respect to a cell of yeast y once that chromosome is introduced into a cell of yeast y.
(25) In contrast, the term “endogenous” as used herein with reference to a nucleic acid (e.g., a gene) or a protein and a host refers to a nucleic acid or protein that does occur in (and can be obtained from) that particular host as it is found in nature. Moreover, a cell “endogenously expressing” a nucleic acid (or protein) expresses that nucleic acid (or protein) as does a host of the same particular type as it is found in nature. Moreover, a host “endogenously producing” or that “endogenously produces” a nucleic acid, protein, or other compound produces that nucleic acid, protein, or compound as does a host of the same particular type as it is found in nature.
(26) For example, depending on the host and the compounds produced by the host, one or more of the following enzymes may be expressed in the host in addition to a malonyl-ACP O-methyltransferase and a pimeloyl-ACP methyl ester methylesterase: a β-ketoacyl-ACP synthase; a β-ketothiolase; a 3-oxoacyl-ACP reductase; acetoacetyl-CoA reductase; a 3-hydroxyacyl-CoA dehydrogenase; a 3-hydroxybutyryl-CoA dehydrogenase; an enoyl-CoA hydratase; 3-hydroxyacyl-ACP dehydratase; an enoyl-ACP reductase; a trans-2-enoyl-CoA reductase; a thioesterase; a reversible CoA ligase; a CoA-transferase; an acetylating aldehyde dehydrogenase; a 6-oxohexanoate dehydrogenase; a 7-oxoheptanoate dehydrogenase; an aldehyde dehydrogenase; a carboxylate reductase; a ω-transaminase; a N-acetyltransferase; an alcohol dehydrogenase; a deacetylase; a 6-hydroxyhexanoate dehydrogenase; a 5-hydroxypentanoate dehydrogenase; a 4-hydroxybutyrate dehydrogenase; a formate-tetrahydrofolate ligase; a S-(hydroxymethyl) glutathione dehydrogenase; or a 5-formylglutathione hydrolase. In recombinant hosts expressing a carboxylate reductase, a phosphopantetheinyl transferase also can be expressed as it enhances activity of the carboxylate reductase.
(27) For example, a recombinant host can include at least one exogenous nucleic acid encoding at least one polypeptide having the activity of: (i) a malonyl-ACP O-methyltransferase, (ii) a β-ketoacyl-ACP synthase or a β-ketothiolase, (iii) a 3-oxoacyl-ACP reductase, acetoacetyl-CoA reductase, a 3-hydroxyacyl-CoA dehydrogenase, or a 3-hydroxybutyryl-CoA dehydrogenase, (iv) an enoyl-CoA hydratase or 3-hydroxyacyl-ACP dehydratase, (v) an enoyl-ACP reductase or a trans-2-enoyl-CoA reductase and produce pimeloyl-ACP or pimeloyl-CoA.
(28) For example, a recombinant host, or non-naturally occurring organism, can include at least one exogenous nucleic acid encoding at least one polypeptide having the activity of at least one enzyme depicted in any of
(29) Such recombinant hosts producing pimeloyl-ACP or pimeloyl-CoA further can include at least one exogenous nucleic acid encoding at least one polypeptide having the activity of a thioesterase, an aldehyde dehydrogenase, a 7-oxoheptanoate dehydrogenase, a 6-oxohexanoate dehydrogenase, a glutaconate CoA-transferase, a reversible succinyl-CoA ligase, an acetylating aldehyde dehydrogenase, or a carboxylate reductase and produce pimelic acid or pimelate semialdehyde. For example, a recombinant host producing pimeloyl-ACP or pimeloyl-CoA further can include a thioesterase, a reversible Co-ligase (e.g., a reversible succinyl-CoA ligase), or a CoA transferase (e.g., a glutaconate CoA-transferase) and produce pimelic acid. For example, a recombinant host producing pimeloyl-CoA further can include an acetylating aldehyde dehydrogenase and produce pimelate semilaldehyde. For example, a recombinant host producing pimelate further can include a carboxylate reductase and produce pimelate semialdehyde.
(30) A recombinant host producing pimelate semialdehyde further can include at least one exogenous nucleic acid encoding at least one polypeptide having the activity of a ω-transaminase and produce 7-aminoheptanoate. In some embodiments, a recombinant host producing pimeloyl-CoA includes a carboxylate reductase and a ω-transaminase to produce 7-aminoheptanoate.
(31) A recombinant host producing pimelate or pimelate semialdehyde further can include at least one exogenous nucleic acid encoding at least one polypeptide having the activity of a 6-hydroxyhexanoate dehydrogenase, a 5-hydroxypentanoate dehydrogenase, or a 4-hydroxybutyrate dehydrogenase, and produce 7-hydroxyheptanoic acid. In some embodiments, a recombinant host producing pimeloyl-CoA includes an acetylating aldehyde dehydrogenase and a 6-hydroxyhexanoate dehydrogenase, a 5-hydroxypentanoate dehydrogenase, or a 4-hydroxybutyrate dehydrogenase to produce 7-hydroxyheptanoate. In some embodiments, a recombinant host producing pimelate includes a carboxylate reductase and a 6-hydroxyhexanoate dehydrogenase, a 5-hydroxypentanoate dehydrogenase, or a 4-hydroxybutyrate dehydrogenase to produce 7-hydroxyheptanoate.
(32) A recombinant host producing 7-aminoheptanoate, 7-hydroxyheptanoate, or pimelate semialdehyde further can include at least one exogenous nucleic acid encoding at least one polypeptide having the activity of a ω-transaminase, a deacetylase, a N-acetyltransferase, or an alcohol dehydrogenase, and produce heptamethylenediamine. For example, a recombinant host producing 7-hydroxyheptanoate can include a carboxylate reductase with an optional phosphopantetheine transferase enhancer, a ω-transaminase, and an alcohol dehydrogenase.
(33) Within an engineered pathway, the enzymes can be from a single source, i.e., from one species, or can be from multiple sources, i.e., different species. Nucleic acids encoding the enzymes described herein have been identified from various organisms and are readily available in publicly available databases such as GenBank or EMBL.
(34) In some embodiments, the host microorganism's endogenous biochemical network is attenuated or augmented to (1) ensure the intracellular availability of acetyl-CoA and malonyl-CoA, (2) create an NAD.sup.+ imbalance that may only be balanced via the formation of a C7 building block, (3) prevent degradation of central metabolites and/or central precursors leading to and including C7 building blocks, (4) ensure efficient efflux from the cell, and/or (5) channel increased flux through the pathway leading to the C7 building block product(s).
(35) Channeling Increased Flux Through C7 Building Block Biosynthesis Pathways
(36) An exemplary pathway (7-AHA pathway) for producing 7-AHA, a C7 building block, is depicted in
(37) Metabolism can often be seen to be resistant to stimulating biosynthesis by expressing or over-expressing pathway enzymes. Control of the flux soon passes elsewhere, and metabolite concentrations rise. A classic metabolic engineering strategy to mitigate this risk is to exploit the natural homeostatic mechanisms of the cell: pull the products out, rather than push precursors toward them. The metabolic network will tend to replace the material that is removed. Feedback loops in the metabolism transfer control from the ‘supply’ steps near the beginning to the ‘demand’ reactions after the feedback loop.
(38) A promising strategy to achieve this ‘flux pulling’ mechanism is to couple the growth of the cell to the formation of a growth critical intermediate produced as part of the biosynthetic pathway. In most cases, this ties growth to yield, titre, and productivity, thus regulating the biosynthesis of the product. This can be achieved by linking the byproduct of methanol, through formate, to the protein synthesis machinery through the tetrahydrofolate metabolic cycle (THF-MC), or a modified THF-MC, and hence growth of the microorganism host. A schematic of the wild-type THF-MC is shown in
(39) Work by Sah et al. (Sah et al., J. Bacteriol., 2015, 197(4), 717-726) investigated the physiological and functional importance of FolD and formyltetrahydrofolate synthetase (Fhs) in the THF-MC. As noted by Sah et al., the enzymes that catalyse interconversions of the above pathway intermediates are highly conserved across the three domains of life (Smith et al., J. Bacteriol., 200, 50, 43-53; Bult et al., Science, 1996, 273, 1058-1073; Slesarev et al., Proc. Natl. Acad. Sci. USA, 2002, 99, 4644-4649; Buchenau et al., Arch. Microbiol., 2004, 182, 313-325; Maeder et al., J. Bacteriol., 2006, 188, 7922-7931). While serine hydroxymethyltransferase (GlyA) catalyses the reversible reaction of conversion of serine and THF to glycine and 5,10-methylene-tetrahydrofolate (5,10-CH2-THF), FolD carries out the conversion of 5,10-methenyltetrahydrofolate (5,10-CH1-THF) to N.sup.10-formyltetrahydrofolate (N.sup.10-fTHF) (see
(40) Many eukaryotic organisms possess FolD (Pino et al., Mol. Microbiol., 2010, 76, 706-718; Paukert et al., J. Biol. Chem., 1976, 251, 5104-5111). Amongst eubacteria, all organisms possess FolD, but some possess both FolD and Fhs (Paukert et al., Biochem. Biophys. Res. Commun., 1977, 77, 147-154). The advantage of possessing Fhs in addition to FolD was demonstrated by Sah et al. (Sah et al., J. Bacteriol., 2015, 197(4), 717-726). In the presence of formate and in anaerobic conditions of growth, predominant synthesis of N.sup.10-fTHF may occur via Fhs. In an fhs-supported E. coli folD deletion (ΔfolD+fhs) model, the enzyme 2-ketobutyrate formate-lyase/pyruvate formate-lyase (pflBtdcE) can produce N.sup.10-fTHF in the presence of formate (see
(41) According to this disclosure, when folD is knocked out and fhs is knocked in or expressed from an exogenously-derived nucleic acid, the microorganism strain should be able to grow after the redirection of the methanol oxidation into the modified THF-MC pathway as the former will act as a source of formate (
(42) The described system may lead to increased yield, titre, and productivity through multiple modes. The described system mitigates the risk of carbon wastage in the system, which results in lower yield. By utilizing the carbon from the methanol byproduct of the BioH enzyme in the 7-AHA pathway, the described system reduces carbon wastage from typical methanol efflux. The described system may also mitigate risk of potential methanol toxicity. Therefore, since the host is dependent on methanol for growth, the accumulation of methanol, which is potentially deleterious to host viability, is decreased. Thus, decreasing methanol accumulation may also mitigate the risk of low 7-AHA yield. Furthermore, the described system may reduce production costs by mitigating the need for methanol removal during downstream processing of the product. As such, the described system has a potential improvement of about 15 to about 22% of the maximum theoretical yield in 7-AHA production, for example.
(43) Thus, by increasing flux through the C7 building block biosynthesis pathway (e.g., the 7-AHA pathway) by requiring methanol for host growth, the biosynthesis of C7 building blocks is regulated.
(44) The attenuation of certain enzymes may contribute to the regulation of biosynthesis of C7 building blocks. For example, a host may have attenuation of a biofunctional protein, classified, for example, under EC 1.5.1.5 and/or under EC 3.5.4.9. For example, and as described above, a host microorganism may have deletion, or knock out, of a bifunctional protein FolD (folD) (see UniProt Accession No. P24186, SEQ ID NO: 32; UniProt Accession No. B7LJI7, SEQ ID NO: 33; UniProt Accession No. Q32JK7, SEQ ID NO: 34).
(45) A host microorganism may also have attenuation of a formate acetyltransferase and/or a pyruvate formate-lyase (PFL)-like enzyme, both of which may be classified under, for example, EC 2.3.1.54. For example, the host may have a deletion, or knock out, of formate acetyltransferase 1 (pflB) (see UniProt Accession No. P09373, SEQ ID NO: 35) and PFL-like enzyme TdcE (tdcE) (see UniProt Accession No. P42632, SEQ ID NO: 36). Formate acetyltransferase 1 synthesizes formate from pyruvate, and PFL-like enzyme TdcE catalyzes the cleavage of 2-ketobutyrate to propionyl-CoA and formate. By removing these two genes, the source of formate is removed. See
(46) The host organism may also express one or more genes encoded in one or more exogenous nucleic acids, or genes may be knocked in to the host organism. For example, as described above, a host organism may express a formylletrahydrofolate synthetase (Fhs), which is interchangeably referred to as a formate-tetrahydrofolate ligase (Fths), and is classified under, for example, EC 6.3.4.3. For example, the host may express one or more Fhs proteins set forth in SEQ ID NOs: 18-22 (see UniProt Accession Nos. Q07064, A8MIN1, P131419, Q5XZD9, and Q251P8, respectively). A formylletrahydrofolate synthetase may be knocked in or expressed from an exogenously-derived nucleic acid.
(47) The host organism may also express an alcohol dehydrogenase (Adh), classified under, for example, EC 1.1.1.-, from one or more exogenous nucleic acids, or the alcohol dehydrogenase may be knocked in to the host organism. For example, the alcohol dehydrogenase may be a methanol dehydrogenase (Mdh), classified under, for example, EC 1.1.1.37. For example, the host may express an alcohol dehydrogenase as set forth in SEQ ID NO: 31 (see UniProt Accession No. Q46856). An alcohol dehydrogenase may then catalyze the conversion of methanol to formaldehyde. Formaldehyde can then be oxidized into formate. See
(48) To aid in oxidation of formaldehyde to formate, the host cell may express a S-(hydroxymethyl) glutathione dehydrogenase (e.g., FrmA), classified under, for example, EC 1.1.1.284, and/or a S-formylglutathione hydrolase (e.g., FrmB), classified under, for example, EC 3.1.2.12, from one or more exogenous nucleic acids, or may be knocked in to the host organism. For example, a host may express a FrmA protein as set forth in SEQ ID NOs: 23-26 (see UniProt Accession Nos. P25437, Q3Z550, A0A0M7MPD4, and W1AV69, respectively) and/or a FrmB protein as set forth in SEQ ID NOs: 27-30 (see UniProt Accession Nos. P51025, Q3Z551, A0A0M9J3Q3, and W1ATJ0, respectively). After formaldehyde spontaneously converts to H-hydroxymethylglutathione, S-(hydroxymethyl) glutathione dehydrogenase converts H-hydroxymethylglutathione to S-formylglutathione. S-formylglutathione hydrolase then converts S-formylglutathione to formate. See
(49) The described system may also lead to using methanol for cell growth. As described above, the modified THF-MC pathway requires methanol as described above, the engineered pathway requires methanol for the synthesis of purine nucleotides, thymidylate, and initiator tRNAs. As such, in this system, methanol is required for cell growth. As such, in the described system, cell growth is reliant on methanol.
(50) Enzymes
(51) Any of the enzymes described herein that can be used for production of one or more C7 building blocks, or in the regulation of the biosynthesis of C7 building blocks, can have at least 50%, at least 60%, or at least 70% sequence identity or homology (e.g., at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 97%, at least 98%, at least 99%, or 100%) to the amino acid sequence of the corresponding wild-type enzyme. It will be appreciated that the sequence identity can be determined on the basis of the mature enzyme (e.g., with any signal sequence removed).
(52) A polypeptide having a certain percent (e.g., at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 97%, at least 98%, at least 99%, or 100%) of sequence identity with another sequence means that, when aligned, that percentage of bases or amino acid residues are the same in comparing the two sequences.
(53) The percent identity and homology between two amino acid sequences can be determined as follows. First, the amino acid sequences are aligned using the BLAST 2 Sequences (Bl2seq) program from the stand-alone version of BLASTZ containing BLASTP version 2.0.14. This stand-alone version of BLASTZ can be obtained from the U.S. government's National Center for Biotechnology Information web site (ncbi.nlm.nih.gov). Instructions explaining how to use the Bl2seq program can be found in the readme file accompanying BLASTZ. Bl2seq performs a comparison between two amino acid sequences using the BLASTP algorithm. To compare two amino acid sequences, the options of Bl2seq are set as follows:—i is set to a file containing the first amino acid sequence to be compared (e.g., C:\seq1.txt); —j is set to a file containing the second amino acid sequence to be compared (e.g., C:\seq2.txt); —p is set to blastp; —o is set to any desired file name (e.g., C:\output.txt); and all other options are left at their default setting. For example, the following command can be used to generate an output file containing a comparison between two amino acid sequences: C: \Bl2seq—i c:\seq1.txt—j c:\seq2.txt—p blastp—o c:\output.txt. If the two compared sequences share homology (identity), then the designated output file will present those regions of homology as aligned sequences. If the two compared sequences do not share homology (identity), then the designated output file will not present aligned sequences. Similar procedures can be following for nucleic acid sequences except that blastn is used.
(54) Once aligned, the number of matches is determined by counting the number of positions where an identical amino acid residue is presented in both sequences. The percent identity is determined by dividing the number of matches by the length of the full-length polypeptide amino acid sequence followed by multiplying the resulting value by 100. It is noted that the percent identity value is rounded to the nearest tenth. For example, 78.11, 78.12, 78.13, and 78.14 is rounded down to 78.1, while 78.15, 78.16, 78.17, 78.18, and 78.19 is rounded up to 78.2. It also is noted that the length value will always be an integer.
(55) When percentage of sequence identity is used in reference to proteins, it is recognized that residue positions which are not identical often differ by conservative amino acid substitutions, where amino acid residues are substituted for other amino acid residues with similar chemical properties (e.g., charge or hydrophobicity) and therefore do not change the functional properties of the molecule. Where sequences differ in conservative substitutions, the percent sequence identity may be adjusted upwards to correct for the conservative nature of the substitution and this process results in “sequence homology” of, e.g., at least 75%, at least 80%, at least 85%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99%. Means for making this adjustment are well known to those of skill in the art. Typically, this involves scoring a conservative substitution as a partial rather than a full mismatch, thereby increasing the percentage sequence identity. Thus, for example, where an identical amino acid is given a score of 1 and a non-conservative substitution is given a score of zero, a conservative substitution is given a score between zero and 1. The scoring of conservative substitutions is calculated, e.g., according to the algorithm of Meyers and Miller, Computer. Applic. Biol. Sci., 1988, 4, 11-17, e.g., as implemented in the program PC/GENE (Intelligenetics, Mountain View, Calif., USA). This alignment and the percent homology or identity can be determined using any suitable software program known in the art, for example those described in CURRENT PROTOCOLS IN MOLECULAR BIOLOGY (F. M. Ausubel et al. (eds.) 1987, Supplement 30, section 7.7.18). Such programs may include the GCG Pileup program, FASTA (Pearson et al., Proc. Natl. Acad. Sci. USA, 1988, 85, 2444-2448), and BLAST (BLAST Manual, Altschul et al., Nat'l Cent. Biotechnol. Inf., Nat'l Lib. Med. (NCIB NLM NIH), Bethesda, Md., and Altschul et al., NAR, 1997, 25, 3389-3402). Another alignment program is ALIGN Plus (Scientific and Educational Software, Pa.), using default parameters. Another sequence software program that finds use is the TFASTA Data Searching Program available in the Sequence Software Package Version 6.0 (Genetics Computer Group, University of Wisconsin, Madison, Wis.).
(56) A conservative substitution is a substitution of one amino acid for another with similar characteristics. Conservative substitutions include substitutions within the following groups: valine, alanine, and glycine; leucine, valine, and isoleucine; aspartic acid and glutamic acid; asparagine and glutamine; serine, cysteine, and threonine; lysine and arginine; and phenylalanine and tyrosine. The nonpolar hydrophobic amino acids include alanine, leucine, isoleucine, valine, proline, phenylalanine, tryptophan, and methionine. The polar neutral amino acids include glycine, serine, threonine, cysteine, tyrosine, asparagine, and glutamine. The positively charged (basic) amino acids include arginine, lysine, and histidine. The negatively charged (acidic) amino acids include aspartic acid and glutamic acid. Any substitution of one member of the above-mentioned polar, basic, or acidic groups by another member of the same group can be deemed a conservative substitution. By contrast, a non-conservative substitution is a substitution of one amino acid for another with dissimilar characteristics.
(57) For example, a thioesterase described herein can have at least 70% sequence identity or homology (e.g., at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 97%, at least 98%, at least 99%, or 100%) to the amino acid sequence of an Escherichia coli thioesterase encoded by tesB (see GenBank Accession No. AAA24665.1, SEQ ID NO: 1).
(58) For example, a carboxylate reductase described herein can have at least 70% sequence identity or homology (e.g., at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 97%, at least 98%, at least 99%, or 100%) to the amino acid sequence of a Mycobacterium marinum (see Genbank Accession No. ACC40567.1, SEQ ID NO: 2), a Mycobacterium smegmatis (see Genbank Accession No. ABK71854.1, SEQ ID NO: 3), a Segniliparus rugosus (see Genbank Accession No. EFV11917.1, SEQ ID NO: 4), a Mycobacterium smegmatis (see Genbank Accession No. ABK75684.1, SEQ ID NO: 5), a Mycobacterium massiliense (see Genbank Accession No. EIV11143.1, SEQ ID NO: 6), or a Segniliparus rotundus (see Genbank Accession No. ADG98140.1, SEQ ID NO: 7) carboxylate reductase.
(59) For example, a ω-transaminase described herein can have at least 70% sequence identity or homology (e.g., at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 97%, at least 98%, at least 99%, or 100%) to the amino acid sequence of a Chromobacterium violaceum (see Genbank Accession No. AAQ59697.1, SEQ ID NO: 8), a Pseudomonas aeruginosa (see Genbank Accession No. AAG08191.1, SEQ ID NO: 9), a Pseudomonas syringae (see Genbank Accession No. AAY39893.1, SEQ ID NO: 10), a Rhodobacter sphaeroides (see Genbank Accession No. ABA81135.1, SEQ ID NO: 11), an Escherichia coli (see RefSeq Accession No. NP_417544.5, SEQ ID NO: 12), or a Vibrio fluvialis (see Genbank Accession No. AEA39183.1, SEQ ID NO: 13) ω-transaminase. Some of these ω-transaminases are diamine ω-transaminases.
(60) For example, a phosphopantetheinyl transferase described herein can have at least 70% sequence identity or homology (e.g., at least 75%, 80%, 85%, 90%, 95%, 97%, 98%, 99%, or 100%) to the amino acid sequence of a Bacillus subtilis phosphopantetheinyl transferase (see RefSeq Accession No. WP_003234549.1, SEQ ID NO: 14) or a Nocardia sp. NRRL 5646 phosphopantetheinyl transferase (see Genbank Accession No. ABI83656.1, SEQ ID NO: 15).
(61) For example, a malonyl-CoA methyltransferase described herein can have at least 70% sequence identity or homology (e.g., at least 75%, 80%, 85%, 90%, 95%, 97%, 98%, 99%, or 100%) to the amino acid sequence of a Bacillus cereus malonyl-CoA methyltransferase (see GenBank Accession No. AAS43086.1, SEQ ID NO: 16).
(62) For example, a pimeloyl-ACP methyl ester esterase described herein can have at least 70% sequence identity or homology (e.g., at least 75%, 80%, 85%, 90%, 95%, 97%, 98%, 99%, or 100%) to the amino acid sequence of an Escherichia coli pimeloyl-ACP methyl ester esterase (see GenBank Accession No. AAC76437.1, SEQ ID NO: 17).
(63) For example, a formate-tetrahydrofolate ligase described herein can have at least 70% sequence identity or homology (e.g., at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 97%, at least 98%, at least 99%, or 100%) to the amino acid sequence of a Clostridium cylindrosporum (see UniProt Accession No. Q07064, SEQ ID NO: 18), an Alkaliphilus oremlandii (see UniProt Accession No. A8MIN1, SEQ ID NO: 19), a Clostridium acidurici (see UniProt Accession No. P13419, SEQ ID NO: 20), a Eubacterium acidaminophilum (see UniProt Accession No. Q5XZD9, SEQ ID NO: 21), or a Desulfitobacterium hafniense (see UniProt Accession No. Q251P8, SEQ ID NO: 22) formate-tetrahydrofolate ligase.
(64) For example, a S-(hydroxymethyl) glutathione dehydrogenase described herein can have at least 70% sequence identity or homology (e.g., at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 97%, at least 98%, at least 99%, or 100%) to the amino acid sequence of a Escherichia coli (see UniProt Accession No. P25437, SEQ ID NO: 23), a Shigella sonnei (see UniProt Accession No. Q3Z550, SEQ ID NO: 24), an Achromaobacter sp. (see UniProt Accession No. A0A0M7MPD4, SEQ ID NO: 25), or a Klebsiella pneumoniae (see UniProt Accession No. W1AV69, SEQ ID NO: 26) S-(hydroxymethyl) glutathione dehydrogenase.
(65) For example, a S-formylglutathione hydrolase described herein can have at least 70% sequence identity or homology (e.g., at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 97%, at least 98%, at least 99%, or 100%) to the amino acid sequence of an Escherichia coli (see UniProt Accession No. P51025, SEQ ID NO: 27), a Shigella sonnei (see UniProt Accession No. Q3Z551, SEQ ID NO: 28), an Achromobacter sp. (see UniProt Accession No. A0A0M9J3Q3, SEQ ID NO: 29), or a Klebsiella pneumoniae (see UniProt Accession No. W1ATJO, SEQ ID NO: 30) S-formylglutathione hydrolase.
(66) For example, an alcohol dehydrogenase described herein can have at least 70% sequence identity or homology (e.g., at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 97%, at least 98%, at least 99%, or 100%) to the amino acid sequence of an Escherichia coli (see UniProt Accession No. Q46856, SEQ ID NO: 31) alcohol dehydrogenase.
(67) It will be appreciated that a number of nucleic acids can encode a polypeptide having a particular amino acid sequence. The degeneracy of the genetic code is well known to the art; i.e., for many amino acids, there is more than one nucleotide triplet that serves as the codon for the amino acid. For example, codons in the coding sequence for a given enzyme can be modified such that optimal expression in a particular species (e.g., bacterium or fungus) is obtained, using appropriate codon bias tables for that species.
(68) Functional fragments of any of the enzymes described herein can also be used in the methods of the disclosure. The term “functional fragment” as used herein refers to a peptide fragment of a protein that has at least 25% (e.g., at least: 30%; 40%; 50%; 60%; 70%; 75%; 80%; 85%; 90%; 95%; 98%; 99%; 100%; or even greater than 100%) of the activity of the corresponding mature, full-length, wild-type protein. The functional fragment can generally, but not always, be comprised of a continuous region of the protein, wherein the region has functional activity.
(69) This disclosure also provides (i) functional variants of the enzymes used in the methods of the disclosure and (ii) functional variants of the functional fragments described above. Functional variants of the enzymes and functional fragments can contain additions, deletions, or substitutions relative to the corresponding wild-type sequences. Enzymes with substitutions will generally have not more than 50 (e.g., not more than one, two, three, four, five, six, seven, eight, nine, ten, 12, 15, 20, 25, 30, 35, 40, or 50) amino acid substitutions (e.g., conservative substitutions). This applies to any of the enzymes described herein and functional fragments. A conservative substitution is a substitution of one amino acid for another with similar characteristics. Conservative substitutions include substitutions within the following groups: valine, alanine and glycine; leucine, valine, and isoleucine; aspartic acid and glutamic acid; asparagine and glutamine; serine, cysteine, and threonine; lysine and arginine; and phenylalanine and tyrosine. The nonpolar hydrophobic amino acids include alanine, leucine, isoleucine, valine, proline, phenylalanine, tryptophan and methionine. The polar neutral amino acids include glycine, serine, threonine, cysteine, tyrosine, asparagine and glutamine. The positively charged (basic) amino acids include arginine, lysine and histidine. The negatively charged (acidic) amino acids include aspartic acid and glutamic acid. Any substitution of one member of the above-mentioned polar, basic or acidic groups by another member of the same group can be deemed a conservative substitution. By contrast, a nonconservative substitution is a substitution of one amino acid for another with dissimilar characteristics.
(70) Deletion variants can lack one, two, three, four, five, six, seven, eight, nine, ten, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 amino acid segments (of two or more amino acids) or non-contiguous single amino acids. Additions (addition variants) include fusion proteins containing: (a) any of the enzymes described herein or a fragment thereof; and (b) internal or terminal (C or N) irrelevant or heterologous amino acid sequences. In the context of such fusion proteins, the term “heterologous amino acid sequences” refers to an amino acid sequence other than (a). A heterologous sequence can be, for example a sequence used for purification of the recombinant protein (e.g., FLAG, polyhistidine (e.g., hexahistidine (SEQ ID NO: 37)), hemagglutinin (HA), glutathione-S-transferase (GST), or maltosebinding protein (MBP)). Heterologous sequences also can be proteins useful as detectable markers, for example, luciferase, green fluorescent protein (GFP), or chloramphenicol acetyl transferase (CAT). In some embodiments, the fusion protein contains a signal sequence from another protein. In certain host cells (e.g., yeast host cells), expression and/or secretion of the target protein can be increased through use of a heterologous signal sequence. In some embodiments, the fusion protein can contain a carrier (e.g., KLH) useful, e.g., in eliciting an immune response for antibody generation) or ER or Golgi apparatus retention signals. Heterologous sequences can be of varying length and in some cases can be a longer sequences than the full-length target proteins to which the heterologous sequences are attached.
(71) Engineered hosts can naturally express none or some (e.g., one or more, two or more, three or more, four or more, five or more, or six or more) of the enzymes of the pathways described herein. Thus, a pathway within an engineered host can include all exogenous enzymes, or can include both endogenous and exogenous enzymes. Endogenous genes of the engineered hosts also can be disrupted to prevent the formation of undesirable metabolites or prevent the loss of intermediates in the pathway through other enzymes acting on such intermediates. Engineered hosts can be referred to as recombinant hosts or recombinant host cells. As described herein recombinant hosts can include nucleic acids encoding one or more of a formate-tetrahydrofolate ligase, a S-(hydroxymethyl) glutathione dehydrogenase, a S-formylglutathione hydrolase, a methyltransferase, a synthase, β-ketothiolase, a dehydratase, a hydratase, a dehydrogenase, a methylesterase, a thioesterase, a reversible CoA-ligase, a CoA-transferase, a reductase, deacetylase, N-acetyltransferase or a ω-transaminase as described in more detail below.
(72) For example, the polynucleotides encoding the described polypeptides, and variants thereof, with the respective enzymatic activity, can be incorporated in a nucleic acid construct or vector. In some embodiments, the polynucleotide is operably linked to one or more heterologous control sequences that direct production of the polypeptide.
(73) In addition, the production of one or more C7 building blocks can be performed in vitro using the isolated enzymes described herein, using a lysate (e.g., a cell lysate) from a host microorganism as a source of the enzymes, or using a plurality of lysates from different host microorganisms as the source of the enzymes.
(74) Enzymes Generating the C7 Aliphatic Backbone for Conversion to C7 Building Blocks
(75) As depicted in
(76) In some embodiments, a methyl ester shielded carbon chain elongation associated with biotin biosynthesis route comprises using a malonyl-ACP O-methyltransferase to form a malonyl-ACP methyl ester, and then performing two cycles of carbon chain elongation using a β-ketoacyl-ACP synthase, a 3-oxoacyl-ACP reductase, a 3-hydroxyacyl-ACP dehydratase, and an enoyl-ACP reductase. A pimeloyl-ACP methyl ester esterase can be used to cleave the resulting pimeloyl-ACP methyl ester.
(77) In some embodiments, a methyl ester shielded carbon chain elongation route comprises using a malonyl-ACP O-methyltransferase to form a malonyl-CoA methyl ester, and then performing two cycles of carbon chain elongation using (i) a β-ketothiolase or a β-ketoacyl-ACP synthase, (ii) an acetoacetyl-CoA reductase, a 3-oxoacyl-ACP reductase, or a 3-hydroxybutyryl-CoA dehydrogenase, (iii) an enoyl-CoA hydratase, and (iv) a trans-2-enoyl-CoA reductase. A pimeloyl-ACP methyl ester esterase can be used to cleave the resulting pimeloyl-CoA methyl ester.
(78) In some embodiments, a methyltransferase can be a malonyl-ACP O-methyltransferase classified, for example, under EC 2.1.1.197, such as, for example, the gene product of bioC from Bacillus cereus (see Genbank Accession No. AAS43086.1, SEQ ID NO: 16) (see, e.g., Lin, 2012, Biotin Synthesis in Escherichia coli, Ph.D. Dissertation, University of Illinois at Urbana-Champaign).
(79) In some embodiments, a β-ketothiolase may be classified, for example, under EC 2.3.1.16, such as, for example, the gene product of bktB. The β-ketothiolase encoded by bktB from Cupriavidus necator accepts propanoyl-CoA and pentanoyl-CoA as substrates, forming the CoA-activated C7 aliphatic backbone (see, e.g., Haywood et al., FEMS Microbiology Letters, 1988, 52:91-96; Slater et al., J. Bacteriol., 1998, 180(8):1979-1987).
(80) In some embodiments, a β-ketoacyl-ACP synthase may be classified, for example, under EC 2.3.1.- (e.g., EC 2.3.1.41, EC 2.3.1.179, or EC 2.3.1.180), such as, for example, the gene product of fabB, fabF, or fabH.
(81) In some embodiments, a 3-hydroxyacyl-CoA dehydrogenase may be classified, for example, under EC 1.1.1.35, such as, for example, the gene product of fadB, or classified under EC 1.1.1.157, such as, for example, the gene product of hbd (can be referred to as a 3-hydroxybutyryl-CoA dehydrogenase), or classified under EC 1.1.1.36, such as, for example, the gene product of phaB (see, e.g., Liu & Chen, Appl. Microbiol. Biotechnol., 2007, 76(5), 1153-1159; Shen et al., Appl. Environ. Microbiol., 2011, 77(9), 2905-2915; or Budde et al., J. Bacteriol., 2010, 192(20), 5319-5328).
(82) In some embodiments, a 3-oxoacyl-CoA reductase may be, for example, classified under EC 1.1.1.100, such as, for example, the gene product of fabG (Budde et al., 2010, supra; Nomura et al., Appl. Environ. Microbiol., 2005, 71(8), 4297-4306).
(83) In some embodiments, an enoyl-CoA hydratase may be classified, for example, under EC 4.2.1.17, such as the gene product of crt, or classified under EC 4.2.1.119, such as, for example, the gene product ofphal (Shen et al., 2011, supra; or Fukui et al., J. Bacteriol., 1998, 180(3), 667-673).
(84) In some embodiments, an enoyl-ACP dehydratase such as a 3-hydroxyacyl-ACP dehydratase may be classified, for example, under EC 4.2.1.59, such as, for example, the gene product of fabZ.
(85) In some embodiments, a trans-2-enoyl-CoA reductase may be classified, for example, under EC 1.3.1.- (e.g., EC 1.3.1.38, EC 1.3.1.8, EC 1.3.1.44), such as, for example, the gene product of ter (Nishimaki et al., J. Biochem., 1984, 95, 1315-1321; Shen et al., 2011, supra) or tdter (Bond-Watts et al., Biochemistry, 2012, 51, 6827-6837).
(86) In some embodiments, an enoyl-ACP reductase may be classified, for example, under EC 1.3.1.10, such as, for example, the gene product of fabL, or EC 1.3.1.9, such as, for example, the gene product of fabI.
(87) In some embodiments, a pimeloyl-ACP methyl ester esterase may be classified, for example, under EC 3.1.1.85, such as, for example, the gene product of bioH from E. coli. See Genbank Accession No. AAC76437.1 (SEQ ID NO: 17).
(88) Enzymes Generating the Terminal Carboxyl Groups in the Biosynthesis of C7 Building Blocks
(89) As depicted in
(90) In some embodiments, the second terminal carboxyl group leading to the synthesis of a C7 building block is enzymatically formed by a thioesterase classified, for example, under EC 3.1.2.-, such as, for example, the gene product of yciA, tesB (Genbank Accession No. AAA24665.1, SEQ ID NO: 1) or acot13 (see, e.g., Cantu et al., Protein Science, 2010, 19, 1281-1295; Zhuang et al., Biochemistry, 2008, 47(9), 2789-2796; or Naggert et al., J. Biol. Chem., 1991, 266(17), 11044-11050).
(91) In some embodiments, the second terminal carboxyl group leading to the synthesis of a C7 building block is enzymatically formed by an acyl-ACP thioesterase classified, for example, under EC 3.1.2.-, such as, for example, the gene product of fatB or tesA. The acyl-ACP thioesterases encoded by Genbank Accession Nos. ABJ63754.1 and CCC78182.1 have C6-C8 chain length specificity (Jing et al., 2011, BMC Biochemistry, 12(44)).
(92) In some embodiments, the second terminal carboxyl group leading to the synthesis of pimelic acid is enzymatically formed by an aldehyde dehydrogenase classified, for example, under EC 1.2.1.3 (see, for example, Guerrillot & Vandecasteele, Eur. J. Biochem., 1977, 81, 185-192).
(93) In some embodiments, the second terminal carboxyl group leading to the synthesis of pimelic acid is enzymatically formed by a dehydrogenase classified, for example, under EC 1.2.1.-, such as, for example, a 6-oxohexanoate dehydrogenase (e.g., the gene product of chnE from Acinetobacter sp.) or a 7-oxoheptanoate dehydrogenase (e.g., such as the gene product of thnG from Sphingomonas macrogolitabida). See, for example, Iwaki et al., Appl. Environ. Microbiol., 1999, 65(11), 5158-5162; or Lopez-Sanchez et al., Appl. Environ. Microbiol., 2010, 76(1), 110-118. For example, a 6-oxohexanoate dehydrogenase can be classified, for example, under EC 1.2.1.63. For example, a 7-oxoheptanoate dehydrogenase can be classified, for example, under EC 1.2.1.-.
(94) In some embodiments, the second terminal carboxyl group leading to the synthesis of pimelic acid is enzymatically formed by a CoA-transferase (e.g., a glutaconate CoA-transferase) classified, for example, under EC 2.8.3.12, such as, for example, a CoA-transferase from Acidaminococcus fermentans. See, for example, Buckel et al., 1981, Eur. J. Biochem., 118:315-321.
(95) In some embodiments, the second terminal carboxyl group leading to the synthesis of pimelic acid is enzymatically formed by a reversible CoA-ligase (e.g., a succinate-CoA ligase) classified, for example, under EC 6.2.1.5, such as, for example, a reversible CoA-ligase from Thermococcus kodakaraensis. See, for example, Shikata et al., 2007, J. Biol. Chem., 282(37):26963-26970.
(96) Enzymes Generating the Terminal Amine Groups in the Biosynthesis of C7 Building Blocks
(97) As depicted in
(98) In some embodiments, the first or second terminal amine group leading to the synthesis of 7-aminoheptanoic acid is enzymatically formed by a ω-transaminase classified, for example, under EC 2.6.1.18, EC 2.6.1.19, EC 2.6.1.29, EC 2.6.1.48, or EC 2.6.1.82, such as, for example, that obtained from Chromobacterium violaceum (Genbank Accession No. AAQ59697.1, SEQ ID NO: 8), Pseudomonas aeruginosa (Genbank Accession No. AAG08191.1, SEQ ID NO: 9), Pseudomonas syringae (Genbank Accession No. AAY39893.1, SEQ ID NO: 10), Rhodobacter sphaeroides (Genbank Accession No. ABA81135.1, SEQ ID NO: 11), Escherichia coli (RefSeq Accession No. NP_417544.5, SEQ ID NO: 12), Vibrio Fluvialis (Genbank Accession No. AEA39183.1, SEQ ID NO: 13), Streptomyces griseus, or Clostridium viride. Some of these ω-transaminases are diamine ω-transaminases (e.g., SEQ ID NO: 12). For example, the ω-transaminases classified, for example, under EC 2.6.1.29 or EC 2.6.1.82 may be diamine ω-transaminases.
(99) The reversible ω-transaminase from Chromobacterium violaceum (Genbank Accession No. AAQ59697.1, SEQ ID NO: 8) has demonstrated analogous activity accepting 6-aminohexanoic acid as amino donor, thus forming the first terminal amine group in adipate semialdehyde (Kaulmann et al., Enzyme and Microbial Technology, 2007, 41, 628-637).
(100) The reversible 4-aminobubyrate:2-oxoglutarate transaminase from Streptomyces griseus has demonstrated analogous activity for the conversion of 6-aminohexanoate to adipate semialdehyde (Yonaha et al., Eur. J. Biochem., 1985, 146:101-106).
(101) The reversible 5-aminovalerate transaminase from Clostridium viride has demonstrated analogous activity for the conversion of 6-aminohexanoate to adipate semialdehyde (Barker et al., J. Biol. Chem., 1987, 262(19), 8994-9003).
(102) In some embodiments, a terminal amine group leading to the synthesis of 7-aminoheptanoate or heptamethylenediamine is enzymatically formed by a diamine ω-transaminase. For example, the second terminal amino group can be enzymatically formed by a diamine ω-transaminase classified, for example, under EC 2.6.1.29 or classified, for example, under EC 2.6.1.82, such as, for example, the gene product of ygjG from E. coli (RefSeq Accession No. NP_417544.5, SEQ ID NO: 12).
(103) The gene product of ygjG accepts a broad range of diamine carbon chain length substrates, such as putrescine, cadaverine and spermidine (see, for example, Samsonova et al., BMC Microbiology, 2003, 3:2).
(104) The diamine ω-transaminase from E. coli strain B has demonstrated activity for 1,7 diaminoheptane (Kim, The Journal of Chemistry, 1964, 239(3), 783-786).
(105) In some embodiments, the second terminal amine group leading to the synthesis of heptamethylenediamine is enzymatically formed by a deacetylase such as acetylputrescine deacetylase classified, for example, under EC 3.5.1.62. The acetylputrescine deacetylase from Micrococcus luteus K-11 accepts a broad range of carbon chain length substrates, such as acetylputrescine, acetylcadaverine and N.sup.8-acetylspermidine (see, for example, Suzuki et al., 1986, BBA—General Subjects, 882(1):140-142).
(106) Enzymes Generating the Terminal Hydroxyl Groups in the Biosynthesis of C7 Building Blocks
(107) As depicted in
(108) In some embodiments, a terminal hydroxyl group leading to the synthesis of 1,7 heptanediol is enzymatically formed by an alcohol dehydrogenase classified, for example, under EC 1.1.1.- (e.g., 1, 2, 21, or 184), such as, for example, the gene product of YMR318C (classified, for example, under EC 1.1.1.2, see Genbank Accession No. CAA90836.1) (Larroy et al., 2002, Biochem J., 361(Pt 1), 163-172), the gene product of yghD, the gene product of cpnD (Iwaki et al., 2002, Appl. Environ. Microbiol., 68(11):5671-5684), the gene product of gbd, or a 6-hydroxyhexanoate dehydrogenase classified, for example, under EC 1.1.1.258, such as, for example, the gene product of chnD (Iwaki et al., Appl. Environ. Microbiol., 1999, supra)
(109) Biochemical Pathways
(110) Pathways Using NADPH-Specific Enzymes to Pimeloyl-ACP as Central Precursor Leading to C7 Building Blocks
(111) In some embodiments, pimeloyl-ACP is synthesized from the central precursor malonyl-ACP, by conversion of malonyl-ACP to malonyl-ACP methyl ester by a malonyl-CoA O-methyltransferase classified, for example, under EC 2.1.1.197, such as, for example, the gene product of bioC; followed by conversion with malonyl-ACP to 3-oxo-glutyryl-ACP methyl ester by a β-ketoacyl-ACP synthase classified, for example, under EC 2.3.1.- (e.g., EC 2.3.1.41, EC 2.3.1.179 or EC 2.3.1.180), such as, for example, the gene product of fabB, fabF, or fabH; followed by conversion to 3-hydroxy-glutaryl-ACP methyl ester by a 3-oxoacyl-ACP reductase classified, for example, under EC 1.1.1.100, such as, for example, the gene product of fabG; followed by conversion to 2,3-dehydroglutaryl-ACP methyl ester by a 3-hydroxyacyl-ACP dehydratase classified, for example, under EC 4.2.1.59, such as, for example, the gene product of fabZ; followed by conversion to glutaryl-ACP methyl ester by an enoyl-ACP reductase classified, for example, under EC 1.3.1.10, such as, for example, the gene product of fabL; followed by conversion to 3-oxo-pimeloyl-ACP methyl ester by a β-ketoacyl-ACP synthase classified, for example, under EC 2.3.1.- (e.g., EC 2.3.1.41 or EC 2.3.1.179), such as, for example, the gene product of fabB or fabF; followed by conversion to 3-hydroxy-pimeloyl-ACP methyl ester by a 3-oxoacyl-ACP reductase classified, for example, under EC 1.1.1.100, such as, for example, the gene product of fabG; followed by conversion to 2,3-dehydropimeloyl-ACP methyl ester by a 3-hydroxyacyl-ACP dehydratase classified, for example, under EC 4.2.1.59, such as, for example, the gene product of fabZ; followed by conversion to pimeloyl-ACP methyl ester by an enoyl-ACP reductase classified, for example, under EC 1.3.1.10, such as, for example, the gene product of fabL; followed by conversion to pimeloyl-ACP by a pimeloyl-ACP methyl ester esterase classified, for example, under EC 3.1.1.85, such as, for example, the gene product of bioH. See
(112) Pathways Using NADPH-Specific Enzymes to Pimeloyl-CoA as Central Precursor Leading to C7 Building Blocks
(113) In some embodiments, pimeloyl-CoA is synthesized from the central precursor malonyl-CoA, by conversion of malonyl-CoA to malonyl-CoA methyl ester by a malonyl-CoA O-methyltransferase classified, for example, under EC 2.1.1.197, such as, for example, the gene product of bioC; followed by conversion with acetyl-CoA to 3-oxo-glutaryl-CoA methyl ester by a β-ketothiolase classified, for example, under EC 2.3.1.16, such as, for example, the gene product of bktB, or by conversion with malonoyl-CoA by a β-ketoacyl-ACP synthase classified, for example, under EC 2.3.1.180, such as, for example, the gene product of fabH; followed by conversion to 3-hydroxy-glutaryl-CoA methyl ester by a 3-oxoacyl-ACP reductase classified, for example, under EC 1.1.1.100, such as, for example, the gene product of fabG, a 3-hydroxyacyl-CoA dehydrogenase classified, for example, under EC 1.1.1.157, such as, for example, the gene product of hbd, or an acetoacetyl-CoA reductase classified, for example, under EC 1.1.1.36 such as the gene product of phaB; followed by conversion to 2,3-dehydroglutaryl-CoA methyl ester by an enoyl-CoA hydratase classified, for example, under EC 4.2.1.119, such as, for example, the gene product of phaf; followed by conversion to glutaryl-CoA methyl ester by a reductase classified, for example, under EC 1.3.1.-, such as, for example, an enoyl-ACP reductase classified under EC 1.3.1.10, such as, for example, the gene product of fabL or a trans-2-enoyl-CoA reductase classified, for example, under EC 1.3.1.38 or EC 1.3.1.8, such as, for example, the gene product of ter or tdter; followed by conversion to 3-oxo-pimeloyl-CoA methyl ester by a β-ketoacyl-ACP synthase classified, for example, under EC 2.3.1.- (e.g., EC 2.3.1.41 or EC 2.3.1.179), such as, for example, the gene product of fabB or fabF, or a β-ketothiolase classified, for example, under EC 2.3.1.16, such as, for example, the gene product of bktB; followed by conversion to 3-hydroxy-pimeloyl-CoA methyl ester by a 3-oxoacyl-ACP reductase classified, for example, under EC 1.1.1.100, such as, for example, the gene product of fabG, a 3-hydroxyacyl-CoA dehydrogenase classified, for example, under EC 1.1.1.157, such as, for example, the gene product of hbd, or an acetoacetyl-CoA reductase classified, for example, under EC 1.1.1.36, such as, for example, the gene product of phaB; followed by conversion to 2,3-dehydropimeloyl-CoA methyl ester by an enoyl-CoA hydratase classified, for example, under EC 4.2.1.119, such as, for example, the gene product of phaf; followed by conversion to pimeloyl-CoA methyl ester by a reductase classified, for example, under EC 1.3.1.-, such as, for example, an enoyl-ACP reductase classified, for example, under EC 1.3.1.10, such as the gene product of fabL, or a trans-2-enoyl-CoA reductase classified under, for example, EC 1.3.1.38 or EC 1.3.1.8, such as, for example, the gene product of ter or tdter; followed by conversion to pimeloyl-CoA by a pimeloyl-ACP methyl ester esterase classified, for example, under EC 3.1.1.85, such as, for example, the gene product of bioH. See
(114) Pathways Using NADH-Specific Enzymes to Pimeloyl-CoA as Central Precursor Leading to C7 Building Blocks
(115) In some embodiments, pimeloyl-CoA is synthesized from the central precursor, malonyl-CoA, by conversion of malonyl-CoA to malonyl-CoA methyl ester by a malonyl-CoA O-methyltransferase classified, for example, under EC 2.1.1.197, such as, for example, the gene product of bioC; followed by conversion with acetyl-CoA to 3-oxo-glutaryl-CoA methyl ester by a β-ketothiolase classified, for example, under EC 2.3.1.16, such as, for example, the gene product of bktB or by conversion with malonyl-CoA by a β-ketoacyl-ACP synthase classified, for example, under EC 2.3.1.180, such as, for example, the gene product of fabH; followed by conversion to 3-hydroxy-glutaryl-CoA methyl ester by a 3-hydroxyacyl-CoA dehydrogenase classified, for example, under EC 1.1.1.- (e.g., EC 1.1.1.35), such as, for example, the gene product of fadB; followed by conversion to 2,3-dehydroglutaryl-CoA methyl ester by an enoyl-CoA hydratase classified, for example, under EC 4.2.1.17, such as, for example, the gene product of crt; followed by conversion to glutaryl-CoA methyl ester by a trans-2-enoyl-CoA reductase classified, for example, under EC 1.3.1.44, such as, for example, the gene product of ter or tdter or an enoyl-ACP reductase classified, for example, under EC 1.3.1.9, such as, for example, the gene product of fabI; followed by conversion to 3-oxopimeloyl-CoA methyl ester by a β-ketoacyl-ACP synthase classified, for example, under EC 2.3.1.- (e.g., EC 2.3.1.41 or EC 2.3.1.179), such as, for example, the gene product of fabB or fabF or a β-ketothiolase classified, for example, under EC 2.3.1.16, such as, for example, the gene product of bktB; followed by conversion to 3-hydroxy-pimeloyl-CoA methyl ester by a 3-hydroxyacyl-CoA dehydrogenase classified, for example, under EC 1.1.1.35, such as, for example, the gene product of fadB; followed by conversion to 2,3-dehydropimeloyl-CoA methyl ester by an enoyl-CoA hydratase classified, for example, under EC 4.2.1.17, such as, for example, the gene product of crt; followed by conversion to pimeloyl-CoA methyl ester by a trans-2-enoyl-CoA reductase classified, for example, under EC 1.3.1.44, such as, for example, the gene product of ter or tdter, or an enoyl-ACP reductase classified, for example, under EC 1.3.1.9, such as, for example, the gene product of fabI; followed by conversion to pimeloyl-CoA by a pimeloyl-ACP methyl ester esterase classified, for example, under EC 3.1.1.85, such as, for example, the gene product of bioH. See
(116) Pathways Using Pimeloyl-CoA or Pimeloyl-ACP as Central Precursors to Pimelate
(117) In some embodiments, pimelic acid is synthesized from the central precursor, pimeloyl-CoA, by conversion of pimeloyl-CoA to pimelate semialdehyde by an acetylating aldehyde dehydrogenase classified, for example, under EC 1.2.1.10, such as, for example, the gene product of pduB or pduP (see, for example, Lan et al., 2013, Energy Environ. Sci., 6:2672-2681); followed by conversion to pimelic acid by a 7-oxoheptanoate dehydrogenase classified, for example, under EC 1.2.1.-, such as, for example, the gene product of thnG, a 6-oxohexanoate dehydrogenase classified, for example, under EC 1.2.1.-, such as, for example, the gene product of chnE, or an aldehyde dehydrogenase classified, for example, under EC 1.2.1.3. See
(118) In some embodiments, pimelic acid is synthesized from the central precursor, pimeloyl-CoA, by conversion of pimeloyl-CoA to pimelate by a thioesterase classified, for example, under EC 3.1.2.-, such as, for example, the gene products of yciA, tesB (Genbank Accession No. AAA24665.1, SEQ ID NO: 1), or acot13. See
(119) In some embodiments, pimelic acid is synthesized from the central precursor, pimeloyl-ACP, by conversion of pimeloyl-ACP to pimelate by a thioesterase classified, for example, under EC 3.1.2.- such as the gene products encoded by Genbank Accession No. ABJ63754.1, Genbank Accession No. CCC78182.1, tesA or fatB. See
(120) In some embodiments, pimelate is synthesized from the central precursor, pimeloyl-CoA, by conversion of pimeloyl-CoA to pimelate by a CoA-transferase such as a glutaconate CoA-transferase classified, for example, under EC 2.8.3.12. See
(121) In some embodiments, pimelate is synthesized from the central precursor, pimeloyl-CoA, by conversion of pimeloyl-CoA to pimelate by a reversible CoA-ligase such as a reversible succinate-CoA ligase classified, for example, under EC 6.2.1.5. See
(122) In some embodiments, pimelate is synthesized from the central precursor, pimelate semialdehyde, by conversion of pimelate semialdehyde to pimelate by a 6-oxohexanoate dehydrogenase or a 7-oxoheptanoate dehydrogenase (classified, for example, under EC 1.2.1.-), such as the gene product of thnG or chnE, or an aldehyde dehydrogenase classified, for example, under EC 1.2.1.3. See
(123) Pathways Using Pimeloyl-CoA or Pimelate Semialdehyde as Central Precursor to 7-Aminoheptanoate
(124) In some embodiments, 7-aminoheptanoate is synthesized from the central precursor, pimeloyl-CoA, by conversion of pimeloyl-CoA to pimelate semialdehyde by an acetylating aldehyde dehydrogenase classified, for example, EC 1.2.1.10, such as, for example, the gene product of pduB or pduP; followed by conversion of pimelate semialdehyde to 7-aminoheptanoate by a ω-transaminase classified, for example, under EC 2.6.1.18, EC 2.6.1.19, EC 2.6.1.29, EC 2.6.1.48, or EC 2.6.1.82. See
(125) In some embodiments, 7-aminoheptanoate is synthesized from the central precursor, pimelate semialdehyde, by conversion of pimelate semialdehyde to 7-aminoheptanoate by a ω-transaminase (e.g., EC 2.6.1.18, EC 2.6.1.19, or EC 2.6.1.48). See
(126) In some embodiments, 7-aminoheptanoate is synthesized from the central precursor, pimelate, by conversion of pimelate to pimelate semialdehyde by a carboxylate reductase classified, for example, under EC 1.2.99.6, such as, for example, the gene product of car optionally in combination with a phosphopantetheine transferase enhancer (e.g., encoded by a sfp (RefSeq Accession No. WP_003234549.1, SEQ ID NO: 14) gene from Bacillus subtilis or npt (Genbank Accession No. ABI83656.1, SEQ ID NO: 15) gene from Nocardia) or the gene products of griC and griD from Streptomyces griseus (Suzuki et al., J. Antibiot., 2007, 60(6), 380-387); followed by conversion of pimelate semialdehyde to 7-aminoheptanoate by a ω-transaminase (e.g., EC 2.6.1.18, EC 2.6.1.19, EC 2.6.1.48, EC 2.6.1.29, or EC 2.6.1.82, such as SEQ ID NOs: 8-13). The carboxylate reductase can be obtained, for example, from Mycobacterium marinum (Genbank Accession No. ACC40567.1, SEQ ID NO: 2), Mycobacterium smegmatis (Genbank Accession No. ABK71854.1, SEQ ID NO: 3), Segniliparus rugosus (Genbank Accession No. EFV11917.1, SEQ ID NO: 4), Mycobacterium smegmatis (Genbank Accession No. ABK75684.1, SEQ ID NO: 5), Mycobacterium massiliense (Genbank Accession No. EIV11143.1, SEQ ID NO: 6), or Segniliparus rotundus (Genbank Accession No. ADG98140.1, SEQ ID NO: 7). See
(127) Pathway Using 7-Aminoheptanoate, 7-Hydroxyheptanoate, or Pimelate Semialdehyde as Central Precursor to Heptamethylenediamine
(128) In some embodiments, heptamethylenediamine is synthesized from the central precursor, 7-aminoheptanoate, by conversion of 7-aminoheptanoate to 7-aminoheptanal by a carboxylate reductase classified, for example, under EC 1.2.99.6, such as, for example, the gene product of car (see above) optionally in combination with a phosphopantetheine transferase enhancer (e.g., encoded by a sfp (RefSeq Accession No. WP_003234549.1, SEQ ID NO: 14) gene from Bacillus subtilis or npt (Genbank Accession No. ABI83656.1, SEQ ID NO: 15) gene from Nocardia) or the gene product of griC and griD; followed by conversion of 7-aminoheptanal to heptamethylenediamine by a ω-transaminase classified, for example, under EC 2.6.1.18, EC 2.6.1.19, EC 2.6.1.29, EC 2.6.1.48, or EC 2.6.1.82, such as SEQ ID NOs: 8-13 (see above). See
(129) The carboxylate reductase encoded by the gene product of car and the phosphopantetheine transferase enhancer npt or sfp has broad substrate specificity, including terminal difunctional C4 and C5 carboxylic acids (Venkitasubramanian et al., Enzyme and Microbial Technology, 2008, 42, 130-137).
(130) In some embodiments, heptamethylenediamine is synthesized from the central precursor, 7-hydroxyheptanoate (which can be produced as described in
(131) In some embodiments, heptamethylenediamine is synthesized from the central precursor, 7-aminoheptanoate, by conversion of 7-aminoheptanoate to N7-acetyl-7-aminoheptanoate by a N-acetyltransferase such as a lysine N-acetyltransferase classified, for example, under EC 2.3.1.32; followed by conversion to N7-acetyl-7-aminoheptanal by a carboxylate reductase classified, for example, under EC 1.2.99.6, such as, for example, the gene product of car (see above) optionally in combination with a phosphopantetheine transferase enhancer (e.g., encoded by a sfp gene from Bacillus subtilis or npt gene from Nocardia) or the gene product of griC and griD; followed by conversion to N7-acetyl-1,7-diaminoheptane by a ω-transaminase classified, for example, under EC 2.6.1.18, EC 2.6.1.19, EC 2.6.1.29, EC 2.6.1.48, EC 2.6.1.46, or EC 2.6.1.82, such as, for example, SEQ ID NOs: 8-13 (see above); followed by conversion to heptamethylenediamine by an acetylputrescine deacylase classified, for example, under EC 3.5.1.62. See,
(132) In some embodiments, heptamethylenediamine is synthesized from the central precursor, pimelate semialdehyde, by conversion of pimelate semialdehyde to heptanedial by a carboxylate reductase classified, for example, under EC 1.2.99.6, such as, for example, the gene product of car (see above) optionally in combination with a phosphopantetheine transferase enhancer (e.g., encoded by a sfp gene from Bacillus subtilis or npt gene from Nocardia) or the gene product of griC and griD; followed by conversion to 7-aminoheptanal by a ω-transaminase classified, for example, under EC 2.6.1.18, EC 2.6.1.19, or EC 2.6.1.48; followed by conversion to heptamethylenediamine by a ω-transaminase classified, for example, under EC 2.6.1.18, EC 2.6.1.19, EC 2.6.1.29, EC 2.6.1.48, EC 2.6.1.46, or EC 2.6.1.82, such as, for example, SEQ ID NOs: 8-13, see above. See
(133) Pathways Using Pimelate or Pimelate Semialdehyde as Central Precursor to 1,7-Heptanediol
(134) In some embodiments, 7-hydroxyheptanoate is synthesized from the central precursor pimelate by conversion of pimelate to pimelate semialdehyde by a carboxylate reductase classified, for example, under EC 1.2.99.6, such as, for example, the gene product of car (see above) optionally in combination with a phosphopantetheine transferase enhancer (e.g., encoded by a sfp gene from Bacillus subtilis or npt gene from Nocardia) or the gene product of griC and griD; followed by conversion to 7-hydroxyheptanoate by a dehydrogenase classified, for example, under EC 1.1.1.-, such as, for example, a 6-hydroxyhexanoate dehydrogenase classified, for example, under EC 1.1.1.258, such as, for example, the gene from of chnD or a 5-hydroxypentanoate dehydrogenase classified, for example, under EC 1.1.1.-, such as, for example, the gene product of cpnD (see, for example, Iwaki et al., 2002, Appl. Environ. Microbiol., 68(11):5671-5684) or a 4-hydroxybutyrate dehydrogenase, such as the gene product of gbd. See
(135) In some embodiments, 1,7 heptanediol is synthesized from the central precursor 7-hydroxyheptanoate by conversion of 7-hydroxyheptanoate to 7-hydroxyheptanal by a carboxylate reductase classified, for example, under EC 1.2.99.6, such as, for example, the gene product of car (see above) optionally in combination with a phosphopantetheine transferase enhancer (e.g., encoded by a sfp gene from Bacillus subtilis or npt gene from Nocardia) or the gene product of griC and griD; followed by conversion of 7-hydroxyheptanal to 1,7 heptanediol by an alcohol dehydrogenase classified, for example, under EC 1.1.1.-, such as, for example, EC 1.1.1.1, EC 1.1.1.2, EC 1.1.1.21, or EC 1.1.1.184, such as, for example, the gene product of YMR318C or yqhD (see, e.g., Liu et al., Microbiology, 2009, 155, 2078-2085; Larroy et al., 2002, Biochem J., 361(Pt 1), 163-172; or Jarboe, 2011, Appl. Microbiol. Biotechnol., 89(2), 249-257) or the protein having GenBank Accession No. CAA81612.1 (from Geobacillus stearothermophilus). See,
(136) Cultivation Strategy
(137) In some embodiments, the cultivation strategy entails achieving an aerobic, anaerobic, or micro-aerobic cultivation condition.
(138) In some embodiments, the cultivation strategy entails nutrient limitation such as nitrogen, phosphate, or oxygen limitation.
(139) In some embodiments, the cultivation strategy for certain recombinant microorganism strains includes addition of specific nutrients or substrates. In some embodiments, the cultivation strategy for a recombinant microorganism strain may include addition of glycine and purine. In some embodiments, the cultivation strategy for a recombinant microorganism strain may include addition of formate. In some embodiments, the cultivation strategy for a recombinant microorganism strain may include addition of formaldehyde. In some embodiments, the cultivation strategy for a recombinant microorganism strain may include addition of methanol.
(140) In some embodiments, a cell retention strategy using, for example, ceramic hollow fiber membranes can be employed to achieve and maintain a high cell density during either fed-batch or continuous fermentation.
(141) In some embodiments, the principal carbon source fed to the fermentation in the synthesis of one or more C7 building blocks can derive from biological or non-biological feedstocks.
(142) In some embodiments, the biological feedstock can be, can include, or can derive from, monosaccharides, disaccharides, lignocellulose, hemicellulose, cellulose, lignin, levulinic acid and formic acid, triglycerides, glycerol, fatty acids, agricultural waste, condensed distillers' solubles, or municipal waste.
(143) The efficient catabolism of crude glycerol stemming from the production of biodiesel has been demonstrated in several microorganisms such as Escherichia coli, Cupriavidus necator, Pseudomonas oleavorans, Pseudomonas putida, and Yarrowia hpolytica (Lee et al., Appl. Biochem. Biotechnol., 2012, 166, 1801-1813; Yang et al., Biotechnology for Biofuels, 2012, 5:13; Meijnen et al., Appl. Microbiol. Biotechnol., 2011, 90, 885-893).
(144) The efficient catabolism of lignocellulosic-derived levulinic acid has been demonstrated in several organisms such as Cupriavidus necator and Pseudomonas putida in the synthesis of 3-hydroxyvalerate via the precursor propanoyl-CoA (Jaremko and Yu, Journal of Biotechnology, 2011, 155, 2011, 293-298; Martin and Prather, Journal of Biotechnology, 2009, 139, 61-67).
(145) The efficient catabolism of lignin-derived aromatic compounds such as benzoate analogues has been demonstrated in several microorganisms such as Pseudomonas putida and Cupriavidus necator (Bugg et al., Current Opinion in Biotechnology, 2011, 22, 394-400; Perez-Pantoja et al., FEMS Microbiol. Rev., 2008, 32, 736-794).
(146) The efficient utilization of agricultural waste, such as olive mill waste water has been demonstrated in several microorganisms, including Yarrowia lipolytica (Papanikolaou et al., Bioresour. Technol., 2008, 99(7), 2419-2428).
(147) The efficient utilization of fermentable sugars such as monosaccharides and disaccharides derived from cellulosic, hemicellulosic, cane and beet molasses, cassava, corn and other agricultural sources has been demonstrated for several microorganism such as Escherichia coli, Corynebacterium glutamicum and Lactobacillus delbrueckii and Lactococcus lactis (see, e.g., Hermann et al., Journal of Biotechnology, 2003, 104, 155-172; Wee et al., Food Technol. Biotechnol., 2006, 44(2), 163-172; Ohashi et al., Journal of Bioscience and Bioengineering, 1999, 87(5), 647-654).
(148) The efficient utilization of furfural, derived from a variety of agricultural lignocellulosic sources, has been demonstrated for Cupriavidus necator (Li et al., Biodegradation, 2011, 22, 1215-1225).
(149) In some embodiments, the non-biological feedstock can be or can derive from natural gas, syngas, CO.sub.2/H.sub.2, methanol, ethanol, benzoic acid, non-volatile residue (NVR), a caustic wash waste stream from cyclohexane oxidation processes, or terephthalic acid/isophthalic acid mixture waste streams.
(150) The efficient catabolism of methanol has been demonstrated for the methylotrophic yeast Pichia pastoris.
(151) The efficient catabolism of ethanol has been demonstrated for Clostridium kluyveri (Seedorf et al., Proc. Natl. Acad. Sci. USA, 2008, 105(6) 2128-2133).
(152) The efficient catabolism of CO.sub.2 and H.sub.2, which may be derived from natural gas and other chemical and petrochemical sources, has been demonstrated for Cupriavidus necator (Prybylski et al., Energy, Sustainability and Society, 2012, 2:11).
(153) The efficient catabolism of syngas has been demonstrated for numerous microorganisms, such as Clostridium ljungdahlii and Clostridium autoethanogenum (Kopke et al., Applied and Environmental Microbiology, 2011, 77(15), 5467-5475).
(154) The efficient catabolism of the non-volatile residue waste stream from cyclohexane processes has been demonstrated for numerous microorganisms, such as Delftia acidovorans and Cupriavidus necator (Ramsay et al., Applied and Environmental Microbiology, 1986, 52(1), 152-156).
(155) In some embodiments, the host microorganism is a prokaryote. For example, the prokaryote can be a bacterium from the genus Escherichia such as Escherichia coli; from the genus Clostridia such as Clostridium ljungdahlii, Clostridium autoethanogenum, or Clostridium kluyveri; from the genus Corynebacteria such as Corynebacterium glutamicum; from the genus Cupriavidus such as Cupriavidus necator or Cupriavidus metallidurans; from the genus Pseudomonas such as Pseudomonas fluorescens, Pseudomonas putida, or Pseudomonas oleavorans; from the genus Delftia such as Delftia acidovorans; from the genus Bacillus such as Bacillus subtillis; from the genus Lactobacillus such as Lactobacillus delbrueckii; or from the genus Lactococcus such as Lactococcus lactis. Such prokaryotes also can be a source of genes to construct recombinant host cells described herein that are capable of producing one or more C7 building blocks.
(156) In some embodiments, the host microorganism is a eukaryote. For example, the eukaryote can be a filamentous fungus, e.g., one from the genus Aspergillus such as Aspergillus niger. Alternatively, the eukaryote can be a yeast, e.g., one from the genus Saccharomyces such as Saccharomyces cerevisiae; from the genus Pichia such as Pichia pastoris; or from the genus Yarrowia such as Yarrowia lipolytica; from the genus Issatchenkia such as Issathenkia orientalis; from the genus Debaryomyces such as Debaryomyces hansenii; from the genus Arxula such as Arxula adenoinivorans; or from the genus Kluyveromyces such as Kluyveromyces lactis. Such eukaryotes also can be a source of genes to construct recombinant host cells described herein that are capable of producing one or more C7 building blocks.
(157) Metabolic Engineering
(158) The present disclosure provides methods involving less than all the steps described for all the above pathways. Such methods can involve, for example, one, two, three, four, five, six, seven, eight, nine, ten, eleven, or twelve or more of such steps. Where less than all the steps are included in such a method, the first, and in some embodiments the only, step can be any one of the steps listed.
(159) Furthermore, recombinant hosts described herein can include any combination of the above enzymes such that one or more of the steps, e.g., one, two, three, four, five, six, seven, eight, nine, or ten or more of such steps, can be performed within a recombinant host. This disclosure provides host cells of any of the genera and species listed and genetically engineered to express one or more (e.g., two, three, four, five, six, seven, eight, nine, 10, 11, or 12 or more) recombinant forms of any of the enzymes recited in the disclosure. Thus, for example, the host cells can contain exogenous nucleic acids encoding enzymes catalyzing one or more of the steps of any of the pathways described herein.
(160) In addition, this disclosure recognizes that where enzymes have been described as accepting CoA-activated substrates, analogous enzyme activities associated with ACP-bound substrates exist that are not necessarily in the same enzyme class.
(161) Also, this disclosure recognizes that where enzymes have been described accepting (R)-enantiomers of substrate, analogous enzyme activities associated with (S)-enantiomer substrates exist that are not necessarily in the same enzyme class.
(162) This disclosure also recognizes that where an enzyme is shown to accept a particular co-factor, such as NADPH, or a co-substrate, such as acetyl-CoA, many enzymes are promiscuous in terms of accepting a number of different co-factors or co-substrates in catalyzing a particular enzyme activity. Also, this disclosure recognizes that where enzymes have high specificity for e.g., a particular co-factor such as NADH, an enzyme with similar or identical activity that has high specificity for the co-factor NADPH may be in a different enzyme class.
(163) In some embodiments, the enzymes in the pathways outlined herein are the result of enzyme engineering via non-direct or rational enzyme design approaches with aims of improving activity, improving specificity, reducing feedback inhibition, reducing repression, improving enzyme solubility, changing stereo-specificity, or changing co-factor specificity.
(164) In some embodiments, the enzymes in the pathways outlined herein can be gene dosed (i.e., overexpressed by having a plurality of copies of the gene in the host organism), into the resulting genetically modified organism via episomal or chromosomal integration approaches.
(165) In some embodiments, genome-scale system biology techniques such as Flux Balance Analysis can be utilized to devise genome scale attenuation or knockout strategies for directing carbon flux to a C7 building block. Knock in and cloning strategies can likewise be devised to direct carbon flux to a C7 building block, as can combinations of attenuation, knock out, knock in, and cloning strategies.
(166) Attenuation of the activity of a particular enzyme can occur through the inhibition of enzymatic activity itself and/or through a decrease in gene expression, including gene deletion/inactivation. Attenuation (decrease in gene expression) and knockout strategies include, but are not limited to: the use of transposons, homologous recombination (double cross-over approach), mutagenesis, non-homologous end joining (NHEJ), Zinc Fingers (ZFs), Transcription-Activator-Like Effectors (TALEs), and the Clustered Regulatory Interspaced Short Palindromic Repeats (CRISPR) sequences with CRISPR-Associated Protein 9 (Cas9) RNA interference (RNAi), double stranded RNA, and enzyme inhibitors. Cloning in strategies include, but are not limited to, inserting a nucleic acid of interest in a vector (e.g., a plasmid, bacteriophage, cosmid, or bacterial artificial chromosome) and inserting the vector into the host cell so that the host cell expresses the nucleic acid of interest. The terms “knocking in” and “cloning in” may both refer to introducing an exogenous nucleic acid into the host cells such that the host cell then expresses the exogenous nucleic acid.
(167) In some embodiments, fluxomic, metabolomics, and transcriptomal data can be utilized to inform or support genome-scale system biology techniques, thereby devising genome scale attenuation or knockout strategies in directing carbon flux to a C7 building block.
(168) In some embodiments, the host microorganism's tolerance to high concentrations of a C7 building block can be improved through continuous cultivation in a selective environment.
(169) In some embodiments, the host microorganism's endogenous biochemical network can be attenuated or augmented to (1) ensure the intracellular availability of acetyl-CoA and malonyl-CoA, (2) create an NADH or NADPH imbalance that may only be balanced via the formation of one or more C7 building blocks, (3) prevent degradation of central metabolites and/or central precursors leading to and including one or more C7 building blocks, (4) ensure efficient efflux from the cell and/or (5) channel increased flux through the pathway leading to the C7 building block product(s).
(170) In some embodiments requiring intracellular availability of acetyl-CoA for C7 building block synthesis, endogenous enzymes catalyzing the hydrolysis acetyl-CoA such as short-chain length thioesterases can be attenuated in the host organism.
(171) In some embodiments requiring condensation of acetyl-CoA and propanoyl-CoA for C7 building block synthesis, one or more endogenous β-ketothiolases catalyzing the condensation of only acetyl-CoA to acetoacetyl-CoA such as the endogenous gene products of AtoB or phaA can be attenuated.
(172) In some embodiments requiring the intracellular availability of acetyl-CoA for C7 building block synthesis, an endogenous phosphotransacetylase generating acetate such as pta can be attenuated (Shen et al., Appl. Environ. Microbiol., 2011, 77(9):2905-2915).
(173) In some embodiments requiring the intracellular availability of acetyl-CoA for C7 building block synthesis, an endogenous gene in an acetate synthesis pathway encoding an acetate kinase, such as ack, can be attenuated.
(174) In some embodiments requiring the intracellular availability of acetyl-CoA and NADH for C7 building block synthesis, an endogenous gene encoding an enzyme that catalyzes the degradation of pyruvate to lactate such as a lactate dehydrogenase encoded by ldhA can be attenuated (Shen et al., 2011, supra).
(175) In some embodiments requiring the intracellular availability of acetyl-CoA and NADH for C7 building block synthesis, endogenous genes encoding enzymes, such as menaquinol-fumarate oxidoreductase, that catalyze the degradation of phophoenolpyruvate to succinate such as frdBC can be attenuated (see, e.g., Shen et al., 2011, supra).
(176) In some embodiments requiring the intracellular availability of acetyl-CoA and NADH for C7 building block synthesis, an endogenous gene encoding an enzyme that catalyzes the degradation of acetyl-CoA to ethanol such as the alcohol dehydrogenase encoded by adhE can be attenuated (Shen et al., 2011, supra).
(177) In some embodiments, where pathways require excess NADH co-factor for C7 building block synthesis, a recombinant formate dehydrogenase gene can be overexpressed in the host organism (Shen et al., 2011, supra).
(178) In some embodiments, where pathways require excess NADH or NADPH co-factor for C7 building block synthesis, an endogenous transhydrogenase dissipating the co-factor imbalance can be attenuated.
(179) In some embodiments, an endogenous gene encoding an enzyme that catalyzes the degradation of pyruvate to ethanol such as pyruvate decarboxylase can be attenuated.
(180) In some embodiments, an endogenous gene encoding an enzyme that catalyzes the generation of isobutanol such as a 2-oxoacid decarboxylase can be attenuated.
(181) In some embodiments requiring the intracellular availability of acetyl-CoA for C7 building block synthesis, a recombinant acetyl-CoA synthetase such as the gene product of acs can be overexpressed in the microorganism (Satoh et al., J. Bioscience and Bioengineering, 2003, 95(4):335-341).
(182) In some embodiments, carbon flux can be directed into the pentose phosphate cycle to increase the supply of NADPH by attenuating an endogenous glucose-6-phosphate isomerase (EC 5.3.1.9).
(183) In some embodiments, carbon flux can be redirected into the pentose phosphate cycle to increase the supply of NADPH by overexpression a 6-phosphogluconate dehydrogenase and/or a transketolase (Lee et al., 2003, Biotechnology Progress, 19(5), 1444-1449).
(184) In some embodiments, where pathways require excess NADPH co-factor in the synthesis of a C7 building block, a gene such as udhA encoding a puridine nucleotide transhydrogenase can be overexpressed in the host organisms (Brigham et al., Advanced Biofuels and Bioproducts, 2012, Chapter 39, 1065-1090).
(185) In some embodiments, where pathways require excess NADPH co-factor in the synthesis of a C7 Building Block, a recombinant glyceraldehyde-3-phosphate-dehydrogenase gene such as gapN can be overexpressed in the host organisms (Brigham et al., 2012, supra).
(186) In some embodiments, where pathways require excess NADPH co-factor in the synthesis of a C7 building block, a recombinant malic enzyme gene such as maeA or maeB can be overexpressed in the host organisms (Brigham et al., 2012, supra).
(187) In some embodiments, where pathways require excess NADPH co-factor in the synthesis of a C7 building block, a recombinant glucose-6-phosphate dehydrogenase gene such as zwf can be overexpressed in the host organisms (Lim et al., J. Bioscience and Bioengineering, 2002, 93(6), 543-549).
(188) In some embodiments, where pathways require excess NADPH co-factor in the synthesis of a C7 building block, a recombinant fructose 1,6 diphosphatase gene such as fbp can be overexpressed in the host organisms (Becker et al., J. Biotechnol., 2007, 132:99-109).
(189) In some embodiments, where pathways require excess NADPH co-factor in the synthesis of a C7 building block, endogenous triose phosphate isomerase (EC 5.3.1.1) can be attenuated.
(190) In some embodiments, where pathways require excess NADPH co-factor in the synthesis of a C7 building block, a recombinant glucose dehydrogenase such as the gene product of gdh can be overexpressed in the host organism (Satoh et al., J. Bioscience and Bioengineering, 2003, 95(4):335-341).
(191) In some embodiments, endogenous enzymes facilitating the conversion of NADPH to NADH can be attenuated, such as the NADH generation cycle that may be generated via inter-conversion of glutamate dehydrogenases classified under EC 1.4.1.2 (NADH-specific) and EC 1.4.1.4 (NADPH-specific). For example, avoiding dissipation of an NADH imbalance towards C7 building blocks, a NADPH-specific glutamate dehydrogenase can be attenuated.
(192) In some embodiments, an endogenous glutamate dehydrogenase (EC 1.4.1.3) that utilizes both NADH and NADPH as co-factors can be attenuated.
(193) In some embodiments, a membrane-bound enoyl-CoA reductases can be solubilized via expression as a fusion protein to a small soluble protein such as a maltose binding protein (Gloerich et al., FEBS Letters, 2006, 580, 2092-2096).
(194) In some embodiments using hosts that naturally accumulate polyhydroxyalkanoates, the endogenous polymer synthase enzymes can be attenuated in the host strain.
(195) In some embodiments, a L-alanine dehydrogenase can be overexpressed in the host to regenerate L-alanine from pyruvate as an amino donor for ω-transaminase reactions.
(196) In some embodiments, a L-glutamate dehydrogenase specific for the co-factor used to achieve co-factor imbalance can be overexpressed in the host to regenerate L-glutamate from 2-oxoglutarate as an amino donor for ω-transaminase reactions. For example, promoting dissipation of the NADH imbalance towards C7 building blocks, a NADH-specific glutamate dehydrogenase can be overexpressed.
(197) In some embodiments, enzymes such as pimeloyl-CoA dehydrogenase classified under, EC 1.3.1.62; an acyl-CoA dehydrogenase classified, for example, under EC 1.3.8.7 or EC 1.3.8.1; and/or a glutaryl-CoA dehydrogenase classified, for example, under EC 1.3.8.6 that degrade central metabolites and/or central precursors leading to and including C7 building blocks can be attenuated.
(198) In some embodiments, endogenous enzymes activating C7 building blocks via Coenzyme A esterification such as CoA-ligases (e.g., a pimeloyl-CoA synthetase) classified under, for example, EC 6.2.1.14 can be attenuated.
(199) In some embodiments, a S-adenosylmethionine synthetase can be overexpressed in the host to generate S-Adenosyl-L-methionine as a co-factor for malonyl-ACP O-methyltransferase.
(200) In some embodiments, an alcohol dehydrogenase, for example a methanol dehydrogenase, and a formaldehyde dehydrogenase can be overexpressed in the host to allow methanol catabolism via formate.
(201) In some embodiments, where the production of formate requires methanol, formate acetyltransferase (e.g., formate acetyltransferase) classified under, for example, EC 2.3.1.54, and/or a pyruvate formate-lyase (PFL)-like enzyme (e.g., pyruvate formate-lyase (PFL)-like enzyme TdcE) classified under, for example, EC 2.3.1.54, can be attenuated.
(202) In some embodiments, where the production of formate requires methanol, an exogenous S-(hydroxymethyl) glutathione dehydrogenase, classified under, for example, EC 1.1.1.284, and/or an exogenous S-formylglutathione hydrolase FrmB classified under, for example, EC 3.1.2.12, can be expressed in the host cell.
(203) In some embodiments, where a modified tetrahydrofolate metabolic cycle requires formate, bifunctional protein FolD (folD) can be attenuated and an exogenous formate-tetrahydrofolate ligase (fhs), classified under, for example, EC 6.3.4.3, can be expressed in the host cell (Sah et al., J. Bacteriology, 2015, 197(4), 717-726).
(204) In some embodiments, the efflux of a C7 building block across the cell membrane to the extracellular media can be enhanced or amplified by genetically engineering structural modifications to the cell membrane or increasing any associated transporter activity for a C7 building block.
(205) The efflux of heptamethylenediamine can be enhanced or amplified by overexpressing broad substrate range multidrug transporters such as Blt from Bacillus subtilis (Woolridge et al., 1997, J. Biol. Chem., 272(14):8864-8866); AcrB and AcrD from Escherichia coli (Elkins & Nikaido, 2002, J. Bacteriol., 184(23), 6490-6499), NorA from Staphylococcus aereus (Ng et al., 1994, Antimicrob Agents Chemother, 38(6), 1345-1355), or Bmr from Bacillus subtilis (Neyfakh, 1992, Antimicrob Agents Chemother, 36(2), 484-485).
(206) The efflux of 7-aminoheptanoate and heptamethylenediamine can be enhanced or amplified by overexpressing the solute transporters such as the lysE transporter from Corynebacterium glutamicum (Bellmann et al., 2001, Microbiology, 147, 1765-1774).
(207) The efflux of pimelic acid can be enhanced or amplified by overexpressing a dicarboxylate transporter such as the SucE transporter from Corynebacterium glutamicum (Huhn et al., Appl. Microbiol. & Biotech., 89(2), 327-335).
(208) Producing C7 Building Blocks Using a Recombinant Host
(209) Typically, one or more C7 building blocks can be produced by providing a host microorganism and culturing the provided microorganism with a culture medium containing a suitable carbon source as described above. In general, the culture media and/or culture conditions can be such that the microorganisms grow to an adequate density and produce a C7 building block efficiently. For large-scale production processes, any method can be used such as those described elsewhere (Manual of Industrial Microbiology and Biotechnology, 2.sup.nd Edition, Editors: A. L. Demain and J. E. Davies, ASM Press; and Principles of Fermentation Technology, P. F. Stanbury and A. Whitaker, Pergamon). Briefly, a large tank (e.g., a 100 gallon, 200 gallon, or 500 gallon or more tank) containing an appropriate culture medium is inoculated with a particular microorganism. After inoculation, the microorganism is incubated to allow biomass to be produced. Once a desired biomass is reached, the broth containing the microorganisms can be transferred to a second tank. This second tank can be any size. For example, the second tank can be larger, smaller, or the same size as the first tank. Typically, the second tank is larger than the first such that additional culture medium can be added to the broth from the first tank. In addition, the culture medium within this second tank can be the same as, or different from, that used in the first tank.
(210) Once transferred, the microorganisms can be incubated to allow for the production of a C7 building block. Once produced, any method can be used to isolate C7 building blocks. For example, C7 building blocks can be recovered selectively from the fermentation broth via adsorption processes. In the case of pimelic acid and 7-aminoheptanoic acid, the resulting eluate can be further concentrated via evaporation, crystallized via evaporative and/or cooling crystallization, and the crystals recovered via centrifugation. In the case of heptamethylenediamine and 1,7-heptanediol, distillation may be employed to achieve the desired product purity.
(211) The invention is further described in the following non-limiting example.
EXAMPLES
(212) Generating a strain that can utilize the methanol byproduct from the 7-AHA pathway as source of formate so that the methanol is an essential intermediate for purines and initiator tRNAs may be accomplished through the proposed cloning strategies discussed below and diagrammed in
Example 1
Cloning Strategy 1
(213) The cloning strategy involves starting with a “pimelate strain” (see
(214) The cloning strategy involves the knocking out folD to produce an fhs-supported E. coli folD deletion (ΔfolD+fhs) model. See
(215) The next strain, strain 4 (
(216) Strain 6 (
Example 2
Cloning Strategy 2
(217) The second cloning strategy also starts with a pimelate strain, as was discussed in Example 1. The host organism in the cloning strategy described in this example is E. coli.
(218) The cloning strategy involves the knocking out folD to produce an fhs-supported E. coli folD deletion (ΔfolD+fhs) model, as described above. See
(219) The next strain (
(220) The final strain, strain 4 (
(221) The proposed cloning strategy is further highlighted in Table 1.
(222) TABLE-US-00001 TABLE 1 Proposed strains and projected outcomes Proposed strain Growth conditions Remarks E. coli pimelate strain Growth on glycerol (FIG. 9, strain 1) fhs-supported E. coli folD Growth on glycerol + A model discussed in Sah deletion (ΔfolD::fhs strain) formate + glycine (+purine) et al. (Sah et al., 2015). (FIG. 9, strain 2) No growth on glycerol Generation of E. coli ΔfolD strain having a single copy of fhs (ΔfolD::fhs) by subjecting the ΔfolD/p-fhs strain to curring of p-fhs. The deletion of folD in E. coli results in autotrophy for purines and glycine. To enable sufficient growth, media may be supplemented with purines and glycine ΔfolD::fhs::frmA::frmB Growth on glycerol + Introduction of frmA and (FIG. 9, strain 3) formaldehyde + glycine frmB enables oxidation of (+purine) formaldehyde to formate No growth on glycerol ΔfolD::fhs::mdh::frmA::frmB Growth on glycerol + Introduction of adh (FIG. 9, strain 4) methanol + glycine (+purine) converts methanol to No growth on glycerol formaldehyde which is then oxidised to formate
(223) The systems described in the predictive examples have a potential improvement of about 15 to about 22% of the maximum theoretical yield in 7-AHA production.