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敲除aceE基因对大肠杆菌生长和丙酮酸代谢的影响
引用本文:宋灿辉,张伟国. 敲除aceE基因对大肠杆菌生长和丙酮酸代谢的影响[J]. 生物加工过程, 2013, 0(6): 15-18
作者姓名:宋灿辉  张伟国
作者单位:江南大学工业生物技术教育部重点实验室,无锡214122
基金项目:国家高技术研究发展计划(863计划)(2008AA02Z212)
摘    要:大肠杆菌aceE基因是编码丙酮酸脱氢酶多酶复合体PdhR的关键酶之一。利用Red重组系统敲除大肠杆菌MG1655的aceE基因后,阻断了丙酮酸流向TCA循环,导致丙酮酸的累积,也使菌体生长受到影响,在培养基中补加5 g/L KAc后可以在一定程度上弥补菌株在生长上的缺陷。摇瓶发酵36 h,MG1655没有积累丙酮酸,MG1655ΔaceE∷cat菌株可以积累26.77 g/L丙酮酸,为利用大肠杆菌发酵生产丙酮酸奠定了基础。

关 键 词:aceE  大肠杆菌  丙酮酸  Red重组

Effects of aceE gene knockout on growing and pyruvate biosynthesis of E. coli
SONG Canhui,ZHANG Weiguo. Effects of aceE gene knockout on growing and pyruvate biosynthesis of E. coli[J]. Chinese Journal of Bioprocess Engineering, 2013, 0(6): 15-18
Authors:SONG Canhui  ZHANG Weiguo
Affiliation:( Key Laboratory of Industrial Biotechnology of the Ministry of Education, Jiangnan University, Wuxi 214122, China)
Abstract:Gene aceE encoding was one of the key enzymes of pyruvate dehydrogenase complex regulator. Using Red recombination, the gene aceE of E. coli MG1655 was knockouted to block the pyruvate flow TCA cycle, causing pyruvate accumulation and growth deficiency. The medium supplemented with 5 g/L KOAc could make up the growth defect to a certain extent strains. MG1655AaceE :: cat in shake flask fermentation for 36 h could produce pyruvate with 26.77 g/L, initial strain MG1655 did not produce pyruvate.
Keywords:aceE  E. coli  pyruvate  Red recombination
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