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重组大肠杆菌全细胞催化L-苏氨酸合成2,5-二甲基吡嗪 被引量:2

Biosynthesis of 2,5-dimethylpyrazine from L-threonine by whole-cell biocatalyst of recombinant Escherichia coli
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摘要 2,5-二甲基吡嗪(2,5-dimethylpyrazine,2,5-DMP)在食品香料与医药方面具有重要的经济价值,工业上普遍采用环境不友好且反应条件苛刻的化学合成法来生产。文中结合代谢工程和辅因子工程策略设计高效催化L-苏氨酸合成2,5-DMP的全细胞催化剂,实现微生物转化法合成2,5-DMP。本研究首先分析了不同微生物来源的苏氨酸脱氢酶(Threonine dehydrogenase,TDH)对2,5-DMP合成的影响,发现来源于大肠杆菌Escherichia coli中EcTDH具有最佳的催化能力,2,5-DMP产量达到(438.3±23.7)mg/L。随后结合辅因子工程,通过引入乳脂链球菌Lactococcus cremoris中NADH氧化酶(NADH oxidase,LcNox E)并优化其表达方式发现通过融合表达EcTDH和Lc Nox E可平衡胞内NADH/NAD+水平,维持较高细胞存活率,进一步提高2,5-DMP产量。最后,通过阻断合成2,5-DMP的支路代谢途径,可以显著减少副产物积累,增加2,5-DMP产量,同时提高L-苏氨酸转化率。最终获得的重组菌EcΔkΔAΔBΔA/TDHEcNoxELc-PSst T在含有5 g/L L-苏氨酸的转化体系中于37℃、200 r/min孵化24 h,可积累(1095.7±81.3)mg/L的2,5-DMP,L-苏氨酸转化率达到76%,产物得率为0.288 g/(g L-苏氨酸)。因此,文中构建的重组菌可以实现高效催化L-苏氨酸合成2,5-DMP,具有一定的工业应用潜力。 2,5-dimethylpyrazine(2,5-DMP)is of important economic value in food industry and pharmaceutical industry,and is now commonly produced by chemical synthesis.In this study,a recombinant Escherichia coli high-efficiently converting L-threonine to 2,5-DMP was constructed by combination of metabolic engineering and cofactor engineering.To do this,the effect of different threonine dehydrogenase(TDH)on 2,5-DMP production was investigated,and the results indicate that overexpression of EcTDH in E.coli BL21(DE3)was beneficial to construct a 2,5-DMP producer with highest 2,5-DMP production.The recombinant strain E.coli p RSFDuet-tdh Ec produced(438.3±23.7)mg/L of 2,5-DMP.Furthermore,the expression mode of NADH oxidase(Nox E)from Lactococcus cremoris was optimized,and fusion expression of EcTDH and Lc Nox E led to balance the intracellular NADH/NAD+level and to maintain the high survival rate of cells,thus further increasing 2,5-DMP production.Finally,the accumulation of by-products was significantly decreased because of disruption of shunt metabolic pathway,thereby increasing 2,5-DMP production and the conversion ratio of L-threonine.Combination of these genetic modifications resulted in an engineered E.coliΔkblΔtynAΔtdcBΔilvA pRSFDuet-tdh EcnoxELc-Psst T(EcΔkΔAΔBΔA/TDHEc Nox ELc-PSst T)capable of producing(1095.7±81.3)mg/L 2,5-DMP with conversion ratio of L-threonine of 76%and a yield of 2,5-DMP of 28.8%in 50 mL transformation system with 5 g/L L-threonine at 37℃and 200 r/min for 24 h.Therefore,this study provides a recombinant E.coli with high-efficiently catalyzing L-threonine to biosynthesize 2,5-DMP,which can be potentially used in biosynthesis of 2,5-DMP in industry.
作者 于海波 徐建中 刘立明 张伟国 Haibo Yu;Jianzhong Xu;Liming Liu;Weiguo Zhang(The Key Laboratory of Industrial Biotechnology of Ministry of Education,School of Biotechnology,Jiangnan University,Wuxi 214122,Jiangsu,China;State Key Laboratory of Food Science and Technology,Jiangnan University,Wuxi 214122,Jiangsu,China)
机构地区 江南大学 江南大学
出处 《生物工程学报》 CAS CSCD 北大核心 2021年第1期228-241,共14页 Chinese Journal of Biotechnology
基金 国家自然科学基金(No.31601459)资助
关键词 2 5-二甲基吡嗪 L-苏氨酸 全细胞催化 EcTDH-LcNoxE融合蛋白 L-苏氨酸转运蛋白SstT 辅因子工程 2,5-dimethylpyrazine L-theronine whole-cell biocatalyst EcTDH-LcNoxE fusion protein L-threonine transporter SstT cofactor engineering
作者简介 Corresponding author:Jianzhong Xu.Tel/Fax:+86-510-85329312,E-mail:xujianzhong@jiangnan.edu.cn
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  • 1Hoessel R, Leclerc S, Endicott JA, et al. Indirubin,the active constituent of a Chinese antileukaemia medicine, inhibits cyclin-dependent kinases. Nat Cell Biol, 1999, 1(1): 60-67.
  • 2Leclerc S, Gamier M, Hoessel R, et al. Indirubins inhibit glycogen synthasekinase-3[3 and CDK5/P25, two protein kinases involved in abnormal tau phosphorylation in Alzheimer's disease. J Biol Chem, 2001, 276(1): 251-260.
  • 3Xiao Z, Hao Y, Liu B, et al. Indirubin and meisoindigo in the treatment of chronic myelogenous leukemia in China. Leu Lymphoma, 2002, 43(1): 1763-1768.
  • 4Kunikata T, Tatefuji T, Aga H, et al. Indirubin inhibits inflammatory reactions in delayed-type hypersensitivity. Eur J Pharmacol, 2000, 410(1): 93-100.
  • 5Gray PHH. The formation of indigotin from indole by soil bacteria. Proc R Soc Lond B Biol Sci, 1928, 102: 263-280.
  • 6Ensley BD, Ratzkin B J, Osslund TD, et al. Expression of naphthalene oxidation genes in Escherichia coli results in the biosynthesis of indigo. Science, 1983, 222(4620): 167-169.
  • 7Bhushan B, Samanta SK, Jain RK. Indigo production by naphthalene-degrading bacteria. Lett Appl Microbiol, 2000, 31: 5-9.
  • 8Pathak H, Madamwar D. Biosythesis of indigo dye by newly isolated naphthalene-degrading strain Pseudomonas sp. HOB1 and its application in dyeing cotton fabric. Appl Bioehem Biotechnol, 2010, 160(6): 1616-1626.
  • 9Mercadal JPR, Isaac P, Sineriz F, et al. Indigo production by Pseudomonas sp. J26, a marine naphthalene-degrading strain. J Basic Microbiol, 2010, 50: 290-293.
  • 10O'Connor KE, Hartmans S. Indigo formation byaromatic hydrocarbon-degarding bacteria. Biotechnol Lett, 1998, 20(3): 219-223.

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