IMMOBILIZED THERMOSTABLE TREHALOSE SYNTHASE AND METHOD FOR PRODUCING TREHALOSE AND TREHALULOSE BY USING SAME
20220186204 · 2022-06-16
Assignee
Inventors
Cpc classification
C12P19/18
CHEMISTRY; METALLURGY
C07K2319/20
CHEMISTRY; METALLURGY
C12R2001/01
CHEMISTRY; METALLURGY
International classification
Abstract
Provided is an immobilized thermostable trehalose synthase including an amino acid sequence of a trehalose synthase domain and an amino acid sequence of a cellulose binding domain. Also provided is a method for converting maltose into trehalose or for converting sucrose into trehalulose by using the immobilized thermostable trehalose synthase.
Claims
1. A thermostable trehalose synthase, comprising: an amino acid sequence of a trehalose synthase domain derived from Thermus thermophilus; and an amino acid sequence of a cellulose binding domain.
2. The thermostable trehalose synthase of claim 1, wherein said amino acid sequence of said cellulose binding domain is derived from Cellulomonas fimi.
3. The thermostable trehalose synthase of claim 1, wherein said amino acid sequence of said cellulose binding domain is connected to a C-terminal of said amino acid sequence of said trehalose synthase domain.
4. The thermostable trehalose synthase of claim 1, which is immobilized on a cellulose, presenting as an immobilized thermostable trehalose synthase.
5. The thermostable trehalose synthase of claim 4, wherein said cellulose is regenerated amorphous cellulose.
6. The thermostable trehalose synthase of claim 1, wherein said amino acid sequence of said trehalose synthase domain has at least 90% sequence identity to SEQ ID NO: 1, and has a same activity as SEQ ID NO: 1.
7. The thermostable trehalose synthase of claim 1, wherein said amino acid sequence of said cellulose binding domain has at least 90% sequence identity to SEQ ID NO: 2, and has a same activity as SEQ ID NO: 2.
8. The thermostable trehalose synthase of claim 1, which has an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 3, and has a same activity as SEQ ID NO: 3.
9. An expression vector for encoding a thermostable trehalose synthase, comprising: a nucleotide sequence for encoding a trehalose synthase domain derived from Thermus thermophiles; and a nucleotide sequence for encoding a cellulose binding domain.
10. The expression vector of claim 9, wherein said nucleotide sequence for encoding said cellulose binding domain is derived from Cellulomonas fimi.
11. The expression vector of claim 9, wherein said nucleotide sequence for encoding said cellulose binding domain is connected to a 3′-terminal of said nucleotide sequence for encoding said trehalose synthase domain.
12. The expression vector of claim 9, wherein said nucleotide sequence for encoding said trehalose synthase domain has at least 90% sequence identity to SEQ ID NO: 4, and has a same activity as SEQ ID NO: 4.
13. The expression vector of claim 9, wherein said nucleotide sequence for encoding said cellulose binding domain has at least 90% sequence identity to SEQ ID NO: 5, and has a same activity as SEQ ID NO: 5.
14. The expression vector of claim 9, which has a nucleotide sequence having at least 90% sequence identity to SEQ ID NO: 6, and has a same activity as SEQ ID NO: 6.
15. A method for producing trehalose, comprising mixing maltose with the thermostable trehalose synthase according to claim 1 to convert said maltose into trehalose.
16. The method of claim 15, further comprising immobilizing the thermostable trehalose synthase on microcrystalline cellulose or regenerated amorphous cellulose to form an immobilized thermostable trehalose synthase.
17. A method for producing trehalulose, comprising mixing sucrose with the thermostable trehalose synthase according to claim 1 to convert said sucrose into trehalulose.
18. The method of claim 17, further comprising immobilizing the thermostable trehalose synthase on microcrystalline cellulose or regenerated amorphous cellulose to form an immobilized thermostable trehalose synthase.
Description
BRIEF DESCRIPTIONS OF THE DRAWINGS
[0028]
[0029]
[0030]
[0031]
[0032]
[0033]
[0034]
DETAILED DESCRIPTION OF THE EMBODIMENTS
[0035] The following aspects of embodiments are used to illustrate the technical contents of the present disclosure. A person having ordinary skill in the art can easily understand the advantages and effects after reading the present disclosure. In addition, all ranges and values herein are inclusive and combinable. Any value or point falling within the range described herein, such as any integer, can be used as the minimum or maximum value to derive the lower range.
[0036] Unless otherwise stated in the context, the singular forms “a/an” and “said” used in the specification and the appended claims include a plurality of individuals, and the term “or” includes the meaning of “and/or.”
[0037] The present disclosure provides a thermostable trehalose synthase, which comprises an amino acid sequence of a trehalose synthase domain and a amino acid sequence of a cellulose binding domain. The present disclosure also provides a recombinant expression vector for encoding said thermostable trehalose synthase and a method for producing trehalose or trehalulose by using said thermostable trehalose synthase.
[0038] In one of the embodiments of the present disclosure, the trehalose synthase domain of the thermostable trehalose synthase may directly convert maltose into trehalose by, for example, converting the α,α-1,4-glycosidic bond of maltose into α,α-1,1-bond. In addition, said trehalose synthase domain may also directly convert sucrose into trehalulose.
[0039] In one of the embodiments of the present disclosure, the amino acid sequence of the trehalose synthase domain and the nucleotide sequence for encoding trehalose synthase domain have at least 90% (e.g., 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100%) sequence identity to SEQ ID NO: 1 and SEQ ID NO: 4, respectively.
[0040] As used herein, the term “sequence identity” means the percentage that the amino acid or nucleotide residues of a candidate protein or nucleic acid fragment are completely identical to the amino acid or nucleotide residue of a reference protein or nucleic acid fragment. When performing the above comparison, said candidate protein or nucleic acid fragment may be aligned, and the gaps may be introduced as necessary, so as to form the highest sequence identity between the two sequences. The amino acid residue where is conservative substitution is regarded as different residue, and the nucleotide residues which are degenerated codons are also regarded as different residues, when calculating the identity; for example, it is considered that there is a different residue U or C between the codons AAU and AAC that both encode asparagine.
[0041] It should be understood that compared to the amino acid or nucleotide sequence of a reference protein or nucleic acid fragment in the present disclosure, amino acid or nucleotide sequence of a candidate protein or nucleic acid fragment, which is modified (e.g., deleted, substituted or added) at least a part in the sequence, is also within the scope of the present disclosure, as long as the resulting candidate protein or nucleic acid fragment has substantially the same biological activity as the amino acid or nucleotide of the reference protein or nucleic acid fragment. This results from the codon degeneracy. In other words, a person having ordinary skill in the art can understand that the amino acid sequence of the trehalose synthase domain and the nucleotide sequence for encoding trehalose synthase domain may have variation, as long as the structure of the active region and the important amino acids in the amino acid sequence of the trehalose synthase domain are not changed, and the effect of converting maltose into trehalose can be achieved.
[0042] Therefore, the nucleotide sequence for encoding trehalose synthase domain provided in the present disclosure may be any nucleotide sequence having the nucleotide sequence of SEQ ID NO: 4 or having at least 90% sequence identity to SEQ ID NO: 4, as long as the protein encoded by said nucleotide sequence can exhibit the activity of the trehalose synthase domain. Similarly, the trehalose synthase domain provided in the present disclosure may be any protein having the amino acid sequence of SEQ ID NO: 1 or homologous to SEQ ID NO: 1, as long as said protein can substantially exhibit the activity of the trehalose synthase domain.
[0043] As used herein, the term “cellulose-binding domain (CBD)” refers to a protein or functional fragment thereof that has a high affinity for cellulose. Cellulose binding domain is discontinuous domains on scaffoldin of cellulosome, wherein the cellulosome is an enzyme complex for cellulose degradation, and is mainly composed of two functional domains, i.e., catalytic domain and cellulose binding domain.
[0044] In the thermostable trehalose synthase of the present disclosure, the cellulose binding domain may be the cellulose binding domain derived from different species. At present, there are more than 200 kinds of cellulose binding domain, and the dominated cellulose binding domain may be found in polysaccharide-degrading enzyme. In addition, cellulose binding domain may also be found in cellulase, hemicellulase, mannanase, xylanase and some non-hydrolyzing proteins. The known cellulose binding domains can be divided into about 39 kinds depending on their amino acid sequences, in which the 6 most common cellulose binding domains are CBD1, CBD2, CBD3, CBD4, CBD5 and CBD9. CBD1 is a cellulose binding domain produced by fungi; CBD2 to CBD5 are cellulose binding domains mainly produced by bacteria; and CBD9 is only found in bacterial xylanase (Ouyang et al., 2008).
[0045] In the thermostable trehalose synthase of the present disclosure, the cellulose binding domain is derived from Cellulomonas fimi. The cellulose binding domain of Cellulomonas fimi has excellent binding ability to microcrystalline cellulose. When cotton fabric is used as a support, the amount of cotton fabric binding to cellulose binding domain can increase with exposure of microcrystalline cellulose during boiling-out; however, the present disclosure is not limited thereto.
[0046] In addition, a person having ordinary skill in the art can understand that the amino acid sequence of the cellulose binding domain and the nucleotide sequence for encoding cellulose binding domain may have variation, as long as the structure of the active region and the important amino acids in the amino acid sequence of the cellulose binding domain are not changed, and the purpose of immobilizing the thermostable trehalose synthase on cellulose can be achieved. Therefore, the nucleotide sequence for encoding cellulose binding domain provided in the present disclosure may be any nucleotide sequence having the nucleotide sequence of SEQ ID NO: 5 or having at least 90% (e.g., 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100%) sequence identity to SEQ ID NO: 5, as long as the protein encoded by said nucleotide sequence can exhibit the activity of the cellulose binding domain. Similarly, the cellulose binding domain of the present disclosure may be any protein having the amino acid sequence of SEQ ID NO: 2 or homologous to SEQ ID NO: 2, as long as said protein can substantially exhibit the activity of the cellulose binding domain.
[0047] In the thermostable trehalose synthase of the present disclosure, the amino acid sequence of the cellulose binding domain is located at C-terminal, and the amino acid sequence of the trehalose synthase domain is located at N-terminal. That is to say, the amino acid sequence of the cellulose binding domain is connected to the C-terminal of the amino acid sequence of the trehalose synthase domain, and there may be an additional amino acid fragment as a linker therebetween, which would not affect enzyme activity. For example, in the thermostable trehalose synthetase of the present disclosure, the amino acid sequence of the cellulose binding domain is connected to the C-terminal of the amino acid sequence of the trehalose synthase domain through a linker, which is a fragment composed of the first to sixth amino acids at the N-terminal of SEQ ID NO: 2.
[0048] In the recombinant expression vector for encoding thermostable trehalose synthase provided in the present disclosure, the nucleotide sequence for encoding cellulose binding domain is connected to the 3′-terminal of the nucleotide sequence for encoding trehalose synthase domain, and there may be an additional nucleotide fragment as a linker therebetween, which would not affect the enzyme expression.
[0049] As used herein, the term “recombinant” refers to the artificial combination of two separate sequence fragments. Generally, the term “recombinant” means that a nucleic acid, protein or microorganism contains genetic material derived from multiple different sources, or is encoded by the genetic material derived from multiple different sources, such as two or more kinds of organisms belonging to different strains or species.
[0050] According to the embodiments of the present disclosure, the thermostable trehalose synthase of the present disclosure is a fusion protein formed by trehalose synthase domain and cellulose binding domain. The thermostable trehalose synthase of the present disclosure may be immobilized on the cellulose through the cellulose binding domain to form an immobilized thermostable trehalose synthase during the reaction, and thus it may be easily separated from reactants or products and may be reused, thereby being conducive to the industrial production of trehalose.
[0051] When the immobilized thermostable trehalose synthase of the present disclosure is used to produce trehalose, the reaction is a single catalytic process and has the advantages such as the preparation process being simple and the reaction process to be easily controlled. Moreover, the immobilized thermostable trehalose synthase of the present disclosure is specific to the substrate, which only works on maltose, but not other sugar such as glucose, maltooligosaccharide and lactose. In addition, the immobilized thermostable trehalose synthase is more conducive to the industrial production of trehalose, because using maltose as substrate may lower the raw material cost.
[0052] The trehalose synthetase provided in the present disclosure has two different converting functions. Under the general conditions of biochemical reaction, said enzyme may convert maltose into trehalose and may also convert sucrose into trehalulose. Both of trehalose and trehalulose may be used in the fields such as food industry, beverages and functional foods, cosmetics, pharmaceutical and biological products.
[0053] Many examples have been used to illustrate the present disclosure. The examples below should not be taken as a limit to the scope of the present disclosure.
EXAMPLES
Example 1
Preparation of the Recombinant Expression Vector
[0054] According to the nucleotide sequence of the trehalose synthase domain (SEQ ID NO: 4) of Thermus thermophiles ATCC 33923 of position 38,394 to position 41,288 of NCBI Accession No. AQOS01000019 and the nucleotide sequence of the cellulose binding domain (SEQ ID NO: 5) of Cellulomonas fimi of position 1,848 to position 2,189 of NCBI Accession No. M15824, a fragment which was the combination of the two sequences and has 3,237 base pairs (SEQ ID NO: 6) was synthesized by full-length gene synthesis. Further, said fragment was cut with restriction enzymes NdeI and SalI, and then ligated with a plasmid pET-20b(+) which was also cut with the same enzymes, so as to obtain a recombinant vector pET-20b(+)-TtTS-CBD. The schematic diagram of pET-20b(+)-TtTS-CBD was shown in
[0055] Afterwards, the recombinant vector was introduced into a commercially available E. coli strain DH5a, and then cultured in an LB medium containing ampicillin with the final concentration of 100 μg/mL. Further, a strain successfully transformed with the recombinant vector was selected.
Example 2
Expression of the Thermostable Trehalose Synthase
[0056] The pET-20b(+)-TtTS-CBD selected in Example 1 was introduced into another strain E. coli Tuner (DE3) pLysS to obtain E. coli Tuner (DE3) pLysS pET-20b(+)-TtTS-CBD transformant.
[0057] Said transformant was cultured in an LB medium containing 100 μg/mL ampicillin and 34 μg/mL chloramphenicol overnight. Subsequently, the cultured transformant was diluted with LB medium containing 100 μg/mL ampicillin, 34 μg/mL chloramphenicol and 0.5 mM isopropyl β-d-1-thiogalactopyranoside (IPTG) in a dilution ratio of 1:50. After incubating at 20° C. for 24 hours, the cells were collected by centrifugation, and then suspended in 20 mM sodium phosphate buffer (pH 7.0) in a volume ratio of 1/10. Furhter, the cells were dissolved/lysed by ultrasonic vibration, and subjected to centrifugation at 10,000×g for 10 minutes, so as to obtain a supernatant (i.e., crude cell extract). Said supernatant contained the recombinant protein having the trehalose synthase domain and the cellulose binding domain (i.e., the thermostable trehalose synthase of the present disclosure).
Example 3
Immobilization of the Recombinant Protein on Microcrystalline Cellulose
[0058] First, 20 mg of microcrystalline cellulose (Type 50, Sigma, St. Louis, Mo.) was added to 10 mL of the crude cell extract prepared in Example 2, and slowly stirred for 1 hour at room temperature. Afterwards, the suspension was centrifuged (8,000×g, 5 minutes, 25° C.), and the supernatant was removed. The cellulose precipitate was washed three times, in which the first washing was performed by a solution containing 2 mL 1 M NaCl and 20 mM sodium phosphate (pH 7), while the other two washings were performed by a solution of 20 mM sodium phosphate (pH 7). Each washing was performed under slowly stirring at room temperature for 30 minutes. After each washing, the suspension was centrifuged (8,000×g, 5 minutes, 25° C.), and the supernatant was removed. After the last washing, the cellulose precipitate was resuspended in 2.5 mL of a solution of 20 mM sodium phosphate (pH 7). The suspension was transferred to a clean test tube and further centrifuged, and then the supernatant was removed. Finally, the fraction attached to the cellulose, the fraction not attached to the cellulose, the washing solutions and the crude cell extract obtained initially were detected by SDS-PAGE analysis.
[0059] The results were shown in
Example 4
Evaluation of the Trehalose Conversion Rate of the Immobilized Enzyme
[0060] With reference to the method described in Example 3, 1 mL crude cell extracts adsorbed on 100 mg of microcrystalline cellulose (i.e., the immobilized enzyme) was prepared, and suspended in 1 mL of a solution of 20 mM sodium phosphate (pH 7). Then, 250 μL of the suspension containing the immobilized enzyme and 750 μL of 40% maltose (dissolved in 20 mM sodium phosphate (pH 7)) were mixed in a rotating mixer and reacted at 60° C. for 24 hours. After the reaction, the contents of maltose, glucose and trehalose in the reaction solution were analyzed by high performance liquid chromatography (HPLC), and then the trehalose conversion rate and the glucose hydrolysis rate were calculated.
[0061] The results were shown in
[0062] In addition, in order to compare the conversion efficiency of the immobilized enzyme and the unimmobilized enzyme, the unimmobilized TtTS-CBD recombinant protein prepared in Example 2 and maltose were reacted according to the aforementioned reaction conditions. The results showed that the trehalose conversion rate of the unimmobilized enzyme was 52.35%, and the glucose hydrolysis rate was 9.47%. It can be seen that the catalytic activity of the immobilized enzyme was slightly increased in comparison with the unimmobilized enzyme, indicating that the immobilization of the recombinant enzyme would not negatively affect the enzyme activity.
Example 5
Evaluation of the Efficiency of the Reused Immobilized Enzyme
[0063] The immobilized enzyme was prepared by the method described in Example 4, and then 25 mg of the immobilized enzyme on microcrystalline cellulose and maltose (dissolved in 20 mM sodium phosphate (pH 7)) were evenly mixed, so as to obtain a reaction solution having a total volume of 1 mL, and the final concentration of maltose being 30%. The reaction solution was then reacted in a rotary mixer at 60° C. for 24 hours, followed by centrifuging at 10,000×g for 5 minutes. The supernatant was collected and stored in a refrigerator at −20° C. for the subsequent HPLC analysis. In addtion, after the centrifugation, the precipitated immobilized enzyme was further mixed and completely suspended in 1 mL of 30% maltose, and reacted in a rotary mixer at 60° C. for 24 hours. The aforementioned enzyme reaction was repeated 7 times.
[0064] The results were shown in
TABLE-US-00001 TABLE 1 Trehalose conversion rate of the reused immobilized enzyme Times of use 1 2 3 4 5 6 7 Glucose (%) 6.19 5.21 4.87 3.84 3.02 2.34 1.70 Maltose (%) 40.42 46.51 48.58 55.95 62.66 70.35 78.06 Trehalose (%) 53.39 48.28 46.55 40.21 34.32 27.30 20.24 Relative conversion 100.0 90.42 87.19 75.32 64.28 51.13 37.91 rate of trehalose (%)
Example 6
Preparation of the Regenerated Amorphous Cellulose
[0065] Regenerated amorphous cellulose (RAC) was prepared from microcrystalline cellulose, and the process was briefly described as follows.
[0066] Firstly, about 0.2 g of microcrystalline cellulose (brand name: Avicel) and 0.6 mL of distilled water were added into a 50 mL centrifuge tube to form a cellulose suspension slurry. Further, 10 mL of cold 86% H3PO4 (commercially available grade, 85%) was slowly added to the slurry under vigorous stirring, and the final concentration of phosphoric acid was calculated as 83.2%. The cellulose mixture became transparent within a few minutes. At the same time, the cellulose mixture was placed in an ice bath and occasionally stirred for 1 hour.
[0067] Next, about 40 mL of ice water was partially added to the cellulose mixture by 10 mL each time, and the mixture was stirred vigorously after each addition of ice water, so as to obtain a white misty precipitate. The obtained cellulose was centrifuged at about 10,000xg at 4° C. for 20 minutes, and the obtained precipitate was suspended in ice water, and then centrifuged to remove phosphoric acid from the supernatant. The foregoing processes were repeated four times in total. Afterwards, the cellulose precipitate was neutralized and suspended in about 0.5 mL of 2 M Na2CO3 and 40 mL of ice distilled water. After centrifugation, the precipitate was washed twice with distilled water, or the pH value thereof reached 5 to 7. Finally, the resulting regenerated amorphous cellulose was suspended in 30 mL of distilled water for later use.
Example 7
Immobilization of the Recombinant Protein on Regenerated Amorphous Cellulose
[0068] With reference to the method described in Example 3, the regenerated amorphous cellulose prepared in Example 6 was subjected to the step of adsorbing the recombinant protein, and analyzed by SDS-PAGE to evaluate the adsorption amount of the amorphous cellulose.
[0069] The results were shown in
[0070] Subsequently, as to the suspension comprising the immobilized enzyme on regenerated amorphous cellulose and the suspension comprising the immobilized enzyme on microcrystalline cellulose, the TtTS-CBD adsorption amounts of the two kinds of cellulose therein were analyzed by protein assay. The results showed that the adsorption capacity of regenerated amorphous cellulose was about 150 times higher than that of microcrystalline cellulose, and the reason might be that the surface area of regenerated amorphous cellulose was higher than that of microcrystalline cellulose.
Example 8
Evaluation of the Efficiency of the Reused Immobilized Enzyme on Regenerated Amorphous Cellulose
[0071] For evaluating the efficiency of the immobilized enzyme on regenerated amorphous cellulose in comparison with the immobilized enzyme on microcrystalline cellulose, the two kinds of immobilized enzymes with about equal amounts of the absorbed recombinant protein TtTS-CBD were independtly mixed with maltose (dissolved in 20 mM sodium phosphate (pH 7)), so as to obtain a reaction solution having a total volume of 1 mL and the final concentration of maltose being 30%. The reaction solution was then reacted in a rotary mixer at 60° C. for 24 hours followed by centrifuging at 11,000 r.p.m. for 5 minutes. The supernatant was collected and stored in a refrigerator at −20° C. for the subsequent HPLC analysis. In addtion, after the centrifugation, the precipitated immobilized enzyme was further mixed and completely suspended in 1 mL of 30% maltose, and reacted in a rotary mixer at 60° C. for 24 hours. The aforementioned enzyme reaction was repeated 7 times.
[0072] The results were shown in
[0073] The results were shown in
TABLE-US-00002 TABLE 2 Trehalose conversion rate of the reused immobilized enzyme on regenerated amorphous cellulose Times of use 1 2 3 4 5 6 7 Trehalose RAC 54.39 49.04 47.30 42.79 29.13 21.46 18.25 (%) C 54.02 48.45 46.01 39.98 35.15 27.30 21.39 Relative RAC 100.00 90.17 86.98 78.68 53.56 39.45 33.56 conversion C 100.00 89.70 85.18 74.02 65.07 50.54 39.59 rate (%)
Example 9
Conversion of Sucrose into Trehalulose by Using the Immobilized Enzyme on Regenerated Amorphous Cellulose
[0074] The suspension containing the immobilized enzyme on regenerated amorphous cellulose was prepared according to the method described in Example 7, and then mixed with a sucrose solution (i.e., 20 mM sodium phosphate (pH 7) in which sucrose was dissolved), so as to obtain a reaction solution containing 0.3 mg/mL of the immobilized enzyme TtTS-CBD on regenerated amorphous cellulose and 30% of the sucrose substrate. The reaction was carried out at 65° C., and the reaction time was 0, 16, 40, or 66 hours. At the end of the reaction, the enzyme reaction was terminated by heating at 99° C. for 10 minutes.
[0075] Afterwards, the resulting sample was filtered with a 4 mm PVDF 0.22 μm syringe filter (MS, SFPVDF004022N), and analyzed by HPLC equipped with an analytical column SUPELCOSIL LC-NH2 4.6×250 (mm). The instrument setting conditions were a flow rate of 1.0 mL/min, column temperature and detector temperature being 40° C., moving phase being acetonitrile: ddH2O=85: 15 v/v%. The results were shown in
[0076] The above-mentioned embodiments are used to exemplify the principles and effects of the present disclosure, but not limit thereto. Those of ordinary skill in the art can modify the above-mentioned embodiments without departing from the scope of the present disclosure. Therefore, the scope of the present disclosure should be set forth in the appended claims.