Recombination strain secreting glutathione and preparation method thereof

A technology of recombinant strains and glutathione, applied in the field of microbial biology, can solve problems such as unfavorable industrialization, and achieve the effects of reducing production costs, improving the possibility of industrialization, and improving the utilization efficiency of raw materials

Active Publication Date: 2013-05-08
镇江市德尔生物制品研究所有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although the fermentation production of GSH by the engineering bacteria constructed by them is the highest yield reported so far, the fermentation process also needs to add toxic compounds such as toluene, which is not conducive to industrialization
In 2004, Perone G.G. et al. expressed gshI and gshII genes and mutated related genes to make yeast ferment and produce GSH to be secreted outside the cell, but the patent reported that the output of shake flask was only 0.06um / L inside the cell and about 0.03umol / L outside the cell[ WO2004 / 003217 A1]

Method used

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  • Recombination strain secreting glutathione and preparation method thereof
  • Recombination strain secreting glutathione and preparation method thereof
  • Recombination strain secreting glutathione and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] Example 1 Construction of glutathione synthesis and transcriptional dysregulated strain X33 (gsh1, gsh2)

[0037] 1) Primers:

[0038] gsh1-1:tgaa GGTACC TTGATCCCGGACGTATCACAGGC (SEQ ID No. 1)

[0039] gsh 1-2:atga TCTAGA ATCAGGCGTGTTTTTCCAGCCAC (SEQ ID No. 2)

[0040] gsh2-1: atca GAATTC ATGATCAAGCTCGGCATCGTGA (SEQ ID No. 3)

[0041] gsh 2-2:atta CTCGAG TTACTGCTGCTGTAAACGTGCTTCxho1 (SEQ ID No. 4)

[0042] GAPG1G2-1: CGGGGTCTGACGCTCAGTGGAACGAAAAC (SEQ ID No. 5)

[0043] GAPG1G2-2:GTAA CCATGG AGTAGAAACATTTTGAAGCTATGGTGT (SEQ ID No. 6)

[0044] 2) Method: In this example, the constitutive promoter GAP was used to express the gsh1 and gsh2 genes derived from Escherichia coli to deregulate GSH transcription. The specific method is as follows:

[0045] The gsh1 gene of Escherichia coli DH5a was amplified by PCR with primers gsh1-1 and gsh1-2. After double digestion with KpnI and XbaI, the plasmid pGAPZB with the same digestion was connected to obtain pGAPG1;...

Embodiment 2

[0048] Example 2 Cut Cysteine ​​to Homocysteine ​​Cycle

[0049] The schematic diagram of cutting off cysteine ​​to homocysteine ​​cycle is as follows figure 2 shown.

[0050] 1) Primers

[0051] Pst3-1-1: 5'TACCAGCAGCAACAGTATGAATGAGATCTC (SEQ ID No. 7)

[0052] Pst3-1-2: 5'GCGTTCCCGTCCAATAATTACTC (1653-1675) (SEQ ID No. 8)

[0053] Pst3-3-1: 5'GTCCTGCCTAAACGTTGCAGTC (2724-2745) (SEQ ID No. 9)

[0054] Pst3-3-2: 5' actactgca GGGGCATCACAGCTCCCTTCTTG (SEQ ID No. 10)

[0055] Pst3-1-3-1-3': GACTGCAACGTTTAGGCAGGACGCGTTCCCGTCAATAATTACTCTGAT (SEQ ID No. 11)

[0056] str3-1-1': TGCCCAGTTCCACCCCTTTCC (SEQ ID No. 12)

[0057] P5Aox-1: AGATCTAACATCCAAAGACGAAAGGTTG (SEQ ID No. 13)

[0058] Pzeo-2: TGGCCTTTTGCTCACATGTTGGTCTCC (SEQ ID No. 14)

[0059] 2) methods (such as image 3 , Str3 gene mutation goes through four steps a, b, c, d)

[0060] ① Str3 gene cloning

[0061] The PCR product with the X33 genome as a template and Pst3-1-1 and Pst3-3-2 as primers was digested with B...

Embodiment 3

[0071] Example 3 Changing the glutathione transport pathway

[0072] The protein encoded by the Hgt1 gene (GeneID: 8200532) is a protein that transports GSH on the cell membrane of yeast methanolica into the cell. Inactivation of the protein methanol yeast may lose the function of absorbing GSH from the outside of the cell. In this example, a mutant of the MRP2 gene expressing the GSH-derived GSH transporter derived from human hepatocytes is used. The MRP2 mutation removes the last three amino acids TKF and relieves the function of anchoring the apical membrane. The MRP2 gene mutant is inserted into the genome at the Hind III restriction site of the Hgt1 gene to inactivate the Hgt1 gene.

[0073] 1) Primers:

[0074] hgt1-1: ATGTCTAGACTGAGTCAGCAG (SEQ ID No. 16)

[0075] hgt1-2: TTACCACCATTTATCAGGAC (SEQ ID No. 17)

[0076] MRP2-1: AATA TTCGAA TGCTGGAGAAGTTCTGCAACTC (SEQ ID No. 18)

[0077] MRP2-2: ATG TACGTA TTAGCTGTTCACATTCTCAATGCCAGC (SEQ ID No. 19)

[0078] GAP2-...

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Abstract

The invention discloses a recombination strain secreting glutathionem, wherein the recombination strain has an inactivated gene of a transportation protein transporting the glutathionem from outside the cell to inside the cell, and expresses a gene of a transportation protein transporting exogenous glutathione from inside the cell to outside the cell. The recombination strain provided by the invention changes transportation pathways of the glutathione, and enables the synthesized glutathione to be secreted to outside of the cells, thereby greatly improving glutathione output, with a concentration of the extracellular glutathione being two times of that of the intracellular glutathione. The recombination strain provided by the invention has a total GSH production of more than 10g/L, and the GSH transported to outside of the cells has a production of more than 7g/L.

Description

technical field [0001] The invention relates to the field of microbial biotechnology, and relates to a recombinant bacterial strain producing glutathione by fermentation and a preparation method thereof. Background technique [0002] Glutathione (GSH) is an important non-protein sulfhydryl compound in organisms, and it is widely used in fields such as medicine and cosmetics, food processing, and protein purification [Sies H. (1999) Free Rad Biol Med.27, 916 -921; Henry Jay Forman et, al, (2009) Molecular Aspects of Medicine 30, 1-12; Zheng Yunlang (1995) Biological Bulletin 30, 22-24; Castro, VM.et, al (1993), Biochem J 292 , 371-377]. [0003] Since the 70s of last century, Kyowa Hakko Kogyo Co. used fermentation to produce glutathione industrialization, fermentation production of GSH has become the main method of its industrial production research [Sakato, K. and Tanaka H.1992, Biotechnol. Bioeng. 40, 904-912]. For this reason, after the seventies in last century, vario...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/19C12N15/09C12P21/02C12R1/84
Inventor 许善峰
Owner 镇江市德尔生物制品研究所有限公司
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