研究报告

产谷胱甘肽毕赤酵母工程菌的构建及能量调控

  • 高宇豪 ,
  • 吴勇杰 ,
  • 朱亚鑫 ,
  • 付静 ,
  • 徐建国 ,
  • 王松涛 ,
  • 徐国强 ,
  • 张晓梅 ,
  • 史劲松 ,
  • 许正宏
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  • 1(江南大学 生物工程学院,江苏 无锡,214122)
    2(工业生物技术教育部重点实验室(江南大学),江苏 无锡,214122)
    3(粮食发酵工艺与技术国家工程实验室(江南大学),江苏 无锡,214122)
    4(江南大学 药学院,江苏 无锡,214122)
    5(无锡福祈制药有限公司,江苏 无锡,214100)
硕士研究生(徐国强副教授为通讯作者,E-mail:xuguoqiang@jiangnan.edu.cn)

收稿日期: 2020-09-15

  修回日期: 2020-10-14

  网络出版日期: 2021-05-20

基金资助

江苏省自然基金面上项目(BK20191333)

Construction and energy regulation of engineered glutathione-producing Pichia pastoris

  • GAO Yuhao ,
  • WU Yongjie ,
  • ZHU Yaxin ,
  • FU Jing ,
  • XU Jianguo ,
  • WANG Songtao ,
  • XU Guoqiang ,
  • ZHANG Xiaomei ,
  • SHI Jinsong ,
  • XU Zhenghong
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  • 1(The Key Laboratory of Industrial Biotechnology,Ministry of Education,Jiangnan University,Wuxi 214122,China)
    2(School of Biotechnology,Jiangnan University,Wuxi 214122,China)
    3(National Engineering Laboratory for Cereal Fermentation Technology,Jiangnan University,Wuxi 214122,China)
    4(School of Pharmaceutical Sciences,Jiangnan University,Wuxi 214122,China)
    5(Wuxi Fuqi Pharmaceutical Co.Ltd.,Wuxi 214100,China)

Received date: 2020-09-15

  Revised date: 2020-10-14

  Online published: 2021-05-20

摘要

谷胱甘肽(glutathione, GSH)是生物体内重要非编码且含有巯基的三肽类物质,具有调节和保护等功能,在医药、食品等领域有着广泛的应用。目前,工业上主要通过高密度发酵生产GSH,ATP的供应往往成为GSH生产的限制因素。该文以毕赤酵母GS115为出发菌株,整合串联表达来源于酿酒酵母的Scgsh1Scgsh2基因,在添加氨基酸前体的条件下,GSH质量浓度可达(302.27±5.06) mg/L,较改造前提高2.88倍。之后优化了柠檬酸钠的添加条件,摇瓶水平最高可达(371.12±8.47) mg/L。最后对工程菌的上罐发酵,通过控制乙醇质量浓度优化葡萄糖的补料速率,实现两阶段高效合成GSH,菌体生物量OD600最高可达257,发酵68 h时GSH产量最高可达2 000 mg/L。该研究为GSH的工业化生产提供了策略参考。

本文引用格式

高宇豪 , 吴勇杰 , 朱亚鑫 , 付静 , 徐建国 , 王松涛 , 徐国强 , 张晓梅 , 史劲松 , 许正宏 . 产谷胱甘肽毕赤酵母工程菌的构建及能量调控[J]. 食品与发酵工业, 2021 , 47(7) : 21 -26 . DOI: 10.13995/j.cnki.11-1802/ts.025672

Abstract

Glutathione is an important non-coding sulfhydryl-containing tripeptide substance in the organism.It has functions such as regulation and protection,and has a wide range of applications in food and medical industries.Recently,glutathione is mainly produced through high cell density fermentation in the industry,and the supply of ATP becomes a limiting factor for GSH production.In this paper, Pichia pastoris GS115 was used as the original strain to heterologously express Scgsh1 and Scgsh2 genes derived from Saccharomyces cerevisiae.With the addition of amino acid precursor, the GSH concentration reached (302.27±5.06) mg/L, which was 2.88 times higher than before.And then, combined with the optimization of sodium citrate addition conditions, the highest GSH concentration in shake flask reached (371.12±8.47) mg/L.Finally, fermentation of the engineered strain was carried out in 100 L tank.By controlling the ethanol concentration to optimize the feed rate of glucose, the two-stage efficient synthesis of glutathione was realized.The maximum biomass OD600 reached 257, and the highest concentration of GSH reached 2 000 mg/L at 68 h.

参考文献

[1] SCHMACHT M,LORENZ E,SENZ M.Microbial production of glutathione[J].World Journal of Microbiology & Biotechology,2017,33(6):106.
[2] 崔筱琳,王凤山.谷胱甘肽防治疾病的研究进展[J].中国现代应用药学,2017,34(4):631-636.
CUI X L,WANG F S.Research progress of glutathione in the prevention and treatment of diseases[J].Chinese Journal of Modern Applied Pharmacy,2017,34(4):631-636.
[3] LU S C.Regulation of glutathione synthesis.[J].Molecular Aspects of Medicine,2009,30(1-2):42-59.
[4] WANG C,ZHANG J,WU H,et al.Heterologous gshF gene expression in various vector systems in Escherichia coli for enhanced glutathione production[J].Journal of Biotechnology,2015,214:63-68.
[5] 王大慧,卫功元.谷胱甘肽的应用前景及生产研究现状[J].化学与生物工程,2004,21(3):10-12.
WANG D H,WEI G Y.The application prospect of glutathione and current research on glutathione production[J].Chemistry & Bioengineering,2004,21(3):10-12.
[6] ZHANG X,WU H,HUANG B,et al.One-pot synthesis of glutathione by a two-enzyme cascade using a thermophilic ATP regeneration system[J].Journal of Biotechnology,2017,241:163-169.
[7] CHEN J L,XIE L,CAI J J,et al.Enzymatic synthesis of glutathione using engineered Saccharomyces cerevisiae[J].Biotechnology Letters,2013,35(8):1 259-1 264.
[8] CAO H,LI C C,ZHAO J,et al.Enzymatic production of glutathione coupling with an ATP regeneration system based on polyphosphate kinase[J].Applied Biochemistry & Biotechnology,2018,185(2):385-395.
[9] SHAO N,WANG D,WEI G,et al.Screening of Candida utilis and medium optimization for co-production of S-adenosylmethionine and glutathione[J].Korean Journal of Chemical Engineering,2010,27(6):1 847-1 853.
[10] ALFAFARA C G,KANDA A,SHIOI T,et al.Effect of amino acids on glutathione production by Saccharomyces cerevisiae[J].Applied Microbiology & Biotechnology,1992,36(4):538-540.
[11] LIANG G B,DU G C,CHEN J.A novel strategy of enhanced glutathione production in high cell density cultivation of Candida utilis—cysteine addition combined with dissolved oxygen controlling[J].Enzyme & Microbial Technology,2008,42(3):284-289.
[12] LIAO X Y,SHEN W,CHEN J,et al.Improved glutathione production by gene expression in Escherichia coli[J].Letters in Applied Microbiology,2010,43(2):211-214.
[13] LIANG G,LIAO X,DU G,et al.Elevated glutathione production by adding precursor amino acids coupled with ATP in high cell density cultivation of Candida utilis[J].Journal of Applied Microbiology,2008,105(5):1 432-1 440.
[14] WANG Y,WANG D,WEI G,et al.Improved co-production of S-adenosylmethionine and glutathione using citrate as an auxiliary energy substrate[J].Bioresource Technology,2013,131:28-32.
[15] CHEN H,CHU J,ZHANG S,et al.Intracellular expression of Vitreoscilla hemoglobin improves S-adenosylmethionine production in a recombinant Pichia pastoris[J].Applied Microbiology & Biotechnology,2007,74(6):1 205-1 212.
[16] RAVI KANT,BALAMURALI M,MEENAKSHISUNDARA M S.Enhancing precursors availability in Pichia pastoris for the overproduction of S-adenosyl-L-methionine employing molecular strategies with process tuning[J].Journal of Biotechnology,2014,188:112-121.
[17] WEN S H.Optimization of the amino acid composition in glutathione fermentation[J].Process Biochemistry,2005.40(11):3 474-3 479.
[18] REN Y,LIU Q,LIU H,et al.Engineering substrate and energy metabolism for living cell production of cytidine-5′-diphosphocholine[J].Biotechnology and Bioengineering,2020,117(5):1 426-1 435.
[19] WU A L,MOYEROWLEY W S.GSH1,which encodes gamma-glutamylcysteine synthetase,is a target gene for yAP-1 transcriptional regulation[J].Molecular and Cellular Biology,1994,14(9):5 832-5 839.
[20] WANG Z,TAN T W,SONG J.Effect of amino acids addition and feedback control strategies on the high-cell-density cultivation of Saccharomyces cerevisiae for glutathione production[J].Process Biochemistry,2007,42(1):108-111.
[21] YANG Z,ZHANG Z.Production of (2R,3R)-2,3-butanediol using engineered Pichia pastoris :Strain construction,characterization and fermentation[J].Biotechnology for Biofuels,2018,11(1):35.
[22] YANG Z,ZHANG Z.Engineering strategies for enhanced production of protein and bio-products in Pichia pastoris:A review[J].Biotechnology Advances,2018,36(1):182-195
[23] SUN X W,LIU H,WANG P,et al.Construction of a novel MK-4 biosynthetic pathway in Pichia pastoris through heterologous expression of HsUBIAD1[J].Microbial Cell Factories,2019,18(1):169.
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