Ean B Mutants and Their Uses

Abstract

Provided herein are a method for producing ergothionine, comprising N (α)-trimethyl histidine and an oxidative sulfurizing enzyme mutant. With the mutant enzyme's help, the conversion rate is higher than 30% with the mutant enzyme amount of 8000/g substrate in 24 hours. Disclosed are a nucleic acid encoding the mutant enzyme, an expression vector comprising the nucleic acid, an expressing host comprising the nucleic acid or the expression vector, and the use of the mutant enzyme EanB for producing the ergothioneine.

Claims

1. An enzyme EanB mutant comprising mutation of one or more changes at position 75, 84 or 369 in amino acid sequence of SEQ ID No 1.

2. The enzyme EanB mutant of claim 1, wherein the mutation is one or two of following changes: (1) I of position 75 is mutated to R; (2) E of position 369 is mutated to P.

3. The EanB enzyme mutant according to claim 1, wherein the mutant comprises an amino acid sequence of SEQ ID NO: 3, SEQ ID NO: 5, or SEQ ID NO: 7.

4. (canceled)

5. (canceled)

6. The EanB enzyme mutant according to claim 3, wherein the EanB enzyme mutant is encoded by a polynucleotide, wherein the polynucleotide comprises a nucleic acid sequence of SEQ ID NO: 4, SEQ ID NO: 6, or SEQ ID NO: 8.

7. (canceled)

8. (canceled)

9. The EanB enzyme mutant according to claim 6, wherein the polynucleotide is located on an expression vector.

10. The vector according to claim 9, wherein the expression vector is pSH plasmid.

11. A host cell comprising the polynucleotide according to claim 6.

12. The host cell according to claim 11, wherein the polynucleotide is located on an expression vector.

13. The host cell according to claim 11, wherein the cell is Escherichia coli.

14. A method of using the EanB enzyme mutant according to claim 1.

15. The method of claim 14, wherein the EanB enzyme mutant is used to produce ergothionine.

16. The host cell according to claim 12, wherein the expression vector is pSH plasmid.

Description

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0020] 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.

[0021] 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.

[0022] In the present invention, enzyme Ean B may be abbreviated as “Ean B” or described as “oxidative sulfurizing enzyme Ean B”

[0023] 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.

[0024] 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.

[0025] 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.

[0026] 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).

[0027] 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.

General Method

[0028] Materials and Method:

[0029] 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.

[0030] 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.

[0031] Culture Medium and Buffer:

[0032] 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.

[0033] The fermentation medium (TB medium): 24 g/L yeast extract, 12 g/L tryptone, 16.43 g/L K.sub.2HPO.sub.4.3 H.sub.2O, 2.31 g/L KH.sub.2PO.sub.4, 5 g/L glycerol, pH 7.0-7.5, autoclaved at 121° C. for 20 min.

[0034] 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.

[0035] 20× electrotransfer stock solution: 80 g/L glycine, 2% Tween 80.

[0036] HPLC Detection of EGT:

[0037] 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.

[0038] EanB Reaction Assay System:

[0039] 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.

[0040] 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).

Example 1. Construction of Oxidative Sulfide Enzyme Expression Strain

[0041] 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.

[0042] 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.

[0043] 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 OD.sub.600 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.

Example 2. Construction of eryK Random Mutation Library by Error-Prone PCR

[0044] A random mutation library was constructed by error-prone PCR using SEQ ID NO: 2 as template.

TABLE-US-00001 Forward primer (EanB-Nde-F): 5′-CATATGCAGAACAAAAACTTTCG-3′, Reverse primer (EanB-Bam-R): 5′-GGATCCTTATTTAGGCACGCCGGTTT-3′.

[0045] 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 MgCl.sub.2, (0 mM, 0.05 mM, 0.1 mM, 0.15 mM, 0.2 mM) MnCl.sub.2, 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 10.sup.4 clones of a random mutation library.

Example 3. High Throughput Screening of EanB Mutant Library

[0046] 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.

[0047] 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.

[0048] 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.

[0049] 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.

TABLE-US-00002 TABLE 1 Comparison of enzyme activities of some EanB mutants Enzyme relative Strain No. Mutant site activity (%)* EanB — 100 EanB-19 I75R 320 EanB-665 K84L, E369P 195 EanB-888 I75R, E369P 480 *Enzyme relative activity: The ratio of the wild-type EanB enzyme activity is set to 100% as control.

[0050] 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.

[0051] 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.

[0052] Thus, the EanB-888 mutant may suitable for mass production of EGT.

Example 4. Construction of High Enzyme Activity Genetic Engineering Microbial Cell

[0053] 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.

[0054] 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.

Example 5. Fermentation of EanB Wild-Type and EanB-888 Mutant Strain

[0055] 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 OD.sub.600 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.

Example 6 the EanB-888 Mutant Catalyzes the Formation of EGT by TMH

[0056] 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.

TABLE-US-00003 TABLE 2 Preparation of EGT by TMH catalyzed by adding different amounts of mutant enzyme EanB-888. Enzyme amount TMH (g/L) (U/g substrate) Conversion rate (%) 10 2000 5.3 4000 8.5 6000 16.4 8000 33 10000 34

[0057] 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.

[0058] According to the table, it can easily get the conclusion that, the mutant EanB-888 make it possible for mass production of EGT.

[0059] 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.