Patent Application
20230024648
The present invention relates to molecular biology, and specifically relates to mutants of enzyme EanB from the green sulfur bacterium Chlorobium limicola. and their uses.
L-ergothionine (EGT), chemically known as 2-mercapto histidine trimethyl inner salt, has the following structuree:
EGT is the only natural 2-thioimidazole amino acid known until now. It has many physiological effects such as anti-oxidation, anti-inflammatory, prolonging cell life cycle and anti-cell aging activity, and nerve cell production improvement. At the same time, it has efficacy in protecting cells and fighting damage in a variety of disease models including complications such as Alzheimer's disease and diabetes. Therefore, EGT has a good market application prospect.
Currently, EGT can be obtained by chemical synthesis, edible fungi extraction and microbial fermentation. A variety of microorganisms have been confirmed can be used to synthesize EGT, such as mycobacteria, Streptomyces, molds, yeast and so on. Among them, the biosynthesis of EGT by edible fungus mycelium deep-fermentation technology is a mainstream direction for low-cost and large-scale production of EGT.
However, there are two important defects in the edible fungus mycelium deep-fermentation technology. Firstly, the growth rate of edible fungus mycelium is slow, resulting in a longer fermentation cycle for generally 7-10 days. Secondly, the EGT synthesized by edible fungus fermentation is mostly accumulated inside the mycelium, a complicated post-treatment process of mycelium like crushing and extraction is required, resulting in a relatively high production cost. Therefore, a method which can easily and quickly produce EGT with a low cost is urgently required.
The objects of the present invention are to provide an enzyme EanB mutant, a nucleic acid sequence encoding the enzyme EanB mutant, an recombinant expression vector comprising the nucleic acid sequence, an expressing host comprising the nucleic acid sequence or the recombinant expression vector, and uses of the enzyme EanB mutants, especially the use of the enzyme Ean B mutant to produce ergothioneine.
In this invention, the enzyme EanB we used was obtained from the green sulfur bacterium Chlorobium limicola. This enzyme can catalyze oxidative sulfurization of N(α)-trimethyl histidine. Under anaerobic condition, enzyme EanB catalyze 6-site C to form C—S bond and synthesise ergothioneine by one-step (Reto, B., et al. (2017). “Anaerobic Origin of Ergothioneine.” Angewandte Chemie International Edition 56(41): 12508-12511; Leisinger, F., et al. (2019). “Structural and Mechanistic Basis for Anaerobic Ergothioneine Biosynthesis.” Journal of the American Chemical Society 141(17): 6906-6914).
Based on wild-type enzyme EanB, the EanB gene mutation library was construction by error-prone PCR mutagenesis, three sites can enhance enzyme activity were then screened out, and an enzyme EanB mutant with significantly improved activity was obtained by site-directed mutagenesis at last.
The present invention relates to the following aspects:
In an embodiment, the present invention provides an enzyme EanB mutant, which comprises mutation of one or more mutant at position 75, 84 or 369 in amino acid sequence of SEQ ID No 1.
In another preferred embodiment, the mutation is one or two of the following changes: (1) the I of position 75 is mutated to R; (2) the E of position 369 is mutated to P.
In particular preferred embodiments, the mutant comprises the amino acid sequence according to any one of SEQ ID NO: 3, 5, or 7.
In an embodiment, the polynucleotide encoding the EanB enzyme mutant of the invention, and the polynucleotide comprises the nucleic acid sequence according to any one of SEQ ID NO: 4, 6, or 8.
In an embodiment, a mutant expression vector comprising the polynucleotide according to any one of SEQ ID NO: 4, 6, or 8.
Preferably, the vector is pSH plasmid comprising the polynucleotide according to any one of SEQ ID NO: 4, 6, or 8.
In an embodiment, a host cell comprising the polynucleotide encoding the EanB enzyme mutant according to any one of SEQ ID NO: 4, 6, or 8.
In an preferred embodiment, a host cell comprising the vector comprising the polynucleotide according to any one of SEQ ID NO: 4, 6, or 8.
Preferably, the host cell is Escherichia col.
The invention also includes the use of the EanB enzyme mutant, preferably, the use of the EanB enzyme mutant of this invention is to produce ergothionine.
While the present invention is capable of being embodied in various forms, the description below of several embodiments is made with the understanding that the present disclosure is to be considered as an exemplification of the claimed subject matter, and is not intended to limit the appended claims to the specific embodiments illustrated and/or described, and should not be construed to limit the scope or breadth of the present disclosure. The headings used throughout this disclosure are provided for convenience only and are not to be construed to limit the claims in any way. Embodiments illustrated under any heading may be combined with embodiments illustrated under any other heading.
The present invention relates to the addition amount, content and concentration of various substances, wherein the percentages are referred to as mass percentages unless otherwise specified. In the examples of the present invention, the temperature generally means room temperature (15-25° C.) if there is no specific explanation made for the reaction temperature or the operating temperature.
In the present invention, enzyme Ean B may be abbreviated as “Ean B” or described as “oxidative sulfurizing enzyme Ean B”
In the present invention, the terms “wild type”, “wild enzyme”, “wild-type enzyme” have the same meaning and refer to the oxidative sulfurizing enzyme EanB (SEQ ID NO: 1) which has not been genetically engineered.
In order to obtain an Ean B mutant with higher enzymatic activity, the present invention performs point mutation of the wild type oxidative sulfurizing enzyme EanB gene sequence SEQ ID NO: 2. The amino acid sequence of one or more amino acid site-substituted mutants was obtained by error-prone PCR technology, three sites for enhancing enzyme activity were screened out, and then one Ean B mutant with significantly improved enzyme activity was obtained by site-directed mutagenesis.
Since the Ean B mutant of the present invention is clear in amino acid sequence, a gene encoding the mutant, an expression assay and plasmid containing the gene, and a transformant comprising the plasmid are easily obtained by those skilled in the art. These genes, expression assays, plasmids, transformants can be obtained by genetic engineering construction methods well known to those skilled in the art.
The transformant host may be any microorganism suitable for expressing an oxidative sulfide enzyme mutant, including bacteria and fungi. Preferably, the microorganisms are Escherichia coli, Pichia pastoris, Saccharomyces cerevisiae, or Bacillus subtilis, preferably Escherichia coli. More preferably, Escherichia coli BL21 (DE3).
When used as a biocatalyst for the production of EGT, the oxidative sulfurizing enzyme of the present invention may be in the form of enzyme or a form of host cells. The forms of the enzyme include free enzyme, immobilized enzyme, purified enzyme, crude enzyme, fermentation broth, carrier-immobilized enzyme, and the like; the forms of the host cell include living cell and dead cell.
Materials and Method:
The separation and purification of the oxidative sulfide enzyme of the present invention, including immobilized enzyme preparation techniques, are also well known to those skilled in the art.
In the present invention, the whole gene synthesis in the present invention was done by Suzhou GENEWIZ, Inc.; the expression vector was prepared by subcloning of Zhejiang Huarui Biotechnology Co., Ltd. Primer synthesis and sequencing were performed by Suzhou GENEWIZ, Inc. Molecular biology experiments include plasmid construction, restriction enzyme digestion, ligation, competent cell preparation, transformation, medium preparation, etc., mainly refer to “Molecular Cloning: A Laboratory Manual” (Third Edition), J. F. Sambrook, D. W. Russell edited, translated by Huang Peitang et al., Science Press, Beijing, 2002). Specific experimental conditions can be determined by simple tests if necessary. PCR amplification experiments were performed according to the reaction conditions or kit instructions provided by the plasmid or DNA template supplier. It can be adjusted by simple experiment if necessary.
Culture Medium and Buffer:
LB medium: 10 g/L tryptone, 10 g/L sodium chloride, 5.0 g/L yeast extract (solid medium added 20 g/L agar powder), pH 7.2, autoclaved at 121° C. for 20 min.
The fermentation medium (TB medium): 24 g/L yeast extract, 12 g/L tryptone, 16.43 g/L K2HPO4.3 H2O, 2.31 g/L KH2PO4, 5 g/L glycerol, pH 7.0-7.5, autoclaved at 121° C. for 20 min.
In the following examples, when an antibiotic-containing medium was used, the final concentration of the antibiotic was 50 μg/ml kanamycin. The corresponding antibiotic was added according to the characteristics of the transformed plasmid.
20× electrotransfer stock solution: 80 g/L glycine, 2% Tween 80.
HPLC Detection of EGT:
Detection conditions: Agilent high performance liquid chromatography 1260 infinity II, Elite ODS-BP column, column temperature 40° C., mobile phase: A, ammonium dihydrogen phosphate (configuration method, take 1.1503 g of ammonium dihydrogen phosphate+400 mL of purified water, adjust the pH with ammonia to 5.0, and add 100 mL of purified water); B: acetonitrile. A:B=99:1, the flow rate is 1 mg/min, the injection volume is 10 μL, and the detection wavelength is 258 nm.
EanB Reaction Assay System:
50 mM phosphate buffer, pH 8.0, 50 mM sodium thiosulfate, 200 mM sodium chloride, 1 mM TMH, 50 μM EanB protein (about 10 mg/ml after purification), 16 hours, 25° C.
Definition of enzyme activity: The enzyme amount required to catalyze the production of 1 micromolar (μmol) of EGT per minute at pH 8.0 and 25° C. is defined as one unit (U).
SEQ ID NO: 2 was obtained by the whole gene synthesis, the restriction enzyme sites NdeI and BamHI were designed at two ends respectively. The sequence was then cloned into the corresponding sites on the pSH plasmid to obtain the recombinant plasmid pSH-EanB, which was then transformed into E. coli expressing strain BL21 (DE3) by electroporation. The cells were cultured overnight at 37° C. on the LB plate coating with 50 μg/ml kanamycin.
Single colonies were selected from the plate and seeded into LB medium with 50 μg/ml kanamycin, after cultured overnight, the cells were collected by centrifugation. The plasmid was extracted and the gene was sequenced correctly, the recombinant strain BL21(DE3)/pSH-EanB expressing wild-type EanB was obtained. The amino acid sequence was determined as SEQ ID NO: 1.
Single colonies were selected from the above plate and inoculated into 5 mL LB medium with 50 μg/ml kanamycin at 37° C. Then, 1% v/v of culture medium was inoculated into 1000 mL flask containing 100 mL fermentation medium, after culturing for 4-6 hours, the OD600 reached 1.2-1.5, the recombination strain was induced by final concentration 0.2 mM of IPTG, and was incubated at 25° C. for 10-16 hours. The cells were obtained by centrifugation and frozen at −80° C. for 24 hours backup.
A random mutation library was constructed by error-prone PCR using SEQ ID NO: 2 as template.
The 50 μL error-prone PCR reaction system includes: 50 ng plasmid template pSH-EanB, 30 pmoles of primer EanB-Nde-F and EanB-Bam-R, 1× Taq buffer, 0.2 mM dGTP, 0.2 mM dATP, 1 mM dCTP, 1 mM dTTP, 7 mM MgCl2, (0 mM, 0.05 mM, 0.1 mM, 0.15 mM, 0.2 mM) MnCl2, 2.5 unit of Taq polymerase (Fermentas). The PCR reaction condition was: 95° C. for 5 min; 94° C. for 30 sec, 55° C. for 30 sec, 72° C. for 2 min/kbp, 30 cycles; 72° C. for 10 min. The 1347 bp random mutant fragment was recovered by gel extraction as a large primer, and the MegaPrimer PCR was performed with KOD-plus DNA polymerase. The PCR condiction was: 94° C. for 5 min; 98° C. for 10 sec, 60° C. for 30 sec, 68° C. for 2 min/kbp, 25 cycles; 68° C. for 10 min. The plasmid template was digested with DpnI and electroporated into E. coli BL21 (DE3) to obtain more than 104 clones of a random mutation library.
The transformants in the EanB mutant library were selected and inoculated into 96-well deep-well culture plates containing 700 μL LB medium with 100 m/mL kanamycin. After incubation for 6 hours at 37° C., final concentration of 0.1 mM IPTG was added. And then the temperature was lowered to 25° C. for overnight incubation. After centrifugation at 5000 rpm for 10 min, the supernatant was discarded, and then frozen at −70° C. for 1 hours, and thawed at room temperature for 30 min. 200 μL of 0.1M potassium phosphate buffer (pH 7.4) was added to resuspend the cells for EanB enzyme activity assay.
80 μL cell suspension (i.e., the enzyme solution) in the above step was added to 80 μL substrate reaction solution (50 mM phosphate buffer, pH 8.0, 50 mM sodium thiosulfate, 200 mM sodium chloride, 1 mM TMH). After reacted at 37° C. for 2 hours, 40 μL termination solution (0.5 ml of a 1M NaOH solution) was added to terminate the reaction, and then centrifuged at 5000 rpm for 10 minutes. The supernatant was took and detected by HPLC to calculate the EanB enzyme activity.
In the random mutation library, four mutant sites for enhancing the activity of EanB enzyme were got by screening about 1000 mutant clones, and the results are shown in Table 1.
To determination and screening of high activity EanB enzyme mutants, the enzyme activities of the respective EanB mutants were screened and determined repeatedly according to the methods described above.
The amino acid sequence of the EanB-888 mutant is SEQ ID NO: 3, the corresponding nucleic acid sequence is SEQ ID NO: 4. The amino acid sequence of the EanB-19 mutant is SEQ ID NO: 5, the corresponding nucleic acid sequence is SEQ ID NO: 6. The amino acid sequence of the EanB-665 mutant is SEQ ID NO: 7, the corresponding nucleic acid sequence is SEQ ID NO: 8.
The enzyme activity of the mutant strain numbered EanB-888 (I75R, E369P) shows the highest enzyme specific activity, which is 4.8-fold higher than that of wild-type enzyme EanB.
Thus, the EanB-888 mutant may suitable for mass production of EGT.
The SEQ ID NO: 4 of the EanB-888 mutant was cloned into the pSH plasmid according to the method of Example 1 to obtain a recombinant plasmid pSH-EanB-888, which was then transformed into E. coli BL21 (DE3) by electroporation. The cells were cultured overnight on the LB plate coated with kanamycin at 37° C. 10 single colonies were selected and inoculated into tubes containing LB medium, after cultured overnight, the cells were collected by centrifugation. The plasmid was extracted and the gene was sequenced correctly, and then the recombinant strain was obtained.
It will be understood by those skilled in the art that the EanB-888 mutant encoding gene including SEQ ID NO: 4 can also be expressed in Bacillus subtilis, Pichia pastoris, Saccharomyces cerevisiae, and the expression host is not limited to E. coli.
Single colonies were selected from the plates of wild type strain and mutant strain, and then inoculated into 5 mL of LB medium at 37° C. Then, 1% v/v of medium was inoculated into 1000 mL flask containing 100 mL of TB medium. After culturing for 4-6 hours, the OD600 reached 1.2-1.5, the cells were induced by adding final concentration of 0.2 mM IPTG, and were incubated at 25° C. for 10-16 hours. The cells were obtained by centrifugation and frozen at −80° C. for 24 hours backup.
The reaction system was 200 mL, the substrate TMH concentration was 10 g/L, and the amounts of added enzyme were 2000, 4000, 6000, 8000, 10000 U/g substrate, respectively. The reaction conditions were at 37° C., 200 rpm, pH 8.0, reacting for 24 hours. The EGT production amount was measured, and the substrate conversion rate was calculated. The results are shown in Table 2.
Form the table, we can see that the conversion rate already gets to 34% with the mutant enzyme amount of 10000 U/g substrate in 24 hours.
According to the table, it can easily get the conclusion that, the mutant EanB-888 make it possible for mass production of EGT.
The above examples demonstrate the process of producing EGT by the mutant enzyme EanB of the present invention, and the relevant process conditions can be further optimized. It should be understood by those skilled in the art that various changes and modifications may be made by those skilled in the art without violating the idea of the present invention.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2019/121260 | 11/27/2019 | WO |
