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敲除iclR基因对大肠杆菌发酵L-色氨酸的影响

陈胜杰 刘辉 谢希贤 徐庆阳 陈宁

天津科技大学学报2016,Vol.31Issue(3):25-30,6.
天津科技大学学报2016,Vol.31Issue(3):25-30,6.DOI:10.13364/j.issn.1672-6510.20150159

敲除iclR基因对大肠杆菌发酵L-色氨酸的影响

Effects of Knockout of GeneiclRonL-tryptophan Fermentation inEscherichia coli

陈胜杰 1刘辉 1谢希贤 1徐庆阳 1陈宁1

作者信息

  • 1. 代谢控制发酵技术国家地方联合工程实验室,天津市氨基酸高效绿色制造工程实验室,天津科技大学生物工程学院,天津 300457
  • 折叠

摘要

Abstract

Escherichia coli TRTH ΔiclRwas constructed via knockout oficlR,the key gene of the glyoxylate shunt in E.coliTRTH through Red recombination to study the effects oficlR knockout onE.coliTRTHL-tryptophan accumula-tion.The results of shake flask fermentation indicated that the yield ofL-tryptophan and the titer ofL-tryptophan from glu-cose ofE.coli TRTH ΔiclRreached(6.52±0.46)g/L and 13.17%,,which were 21.86%, and 22.85%, higher than those ob-tained fromE.coli TRTH,respectively;6.82,g/L of acetic acid accumulated in the culture ofE.coli TRTH ΔiclR,which was 37.63%, lower than that of the control strain.In the fermentation of 30,L fermenter,the titer and yield ofL-tryptophan of E.coli TRTH ΔiclR were(13.01±1.05)g/L and 6.51%,,which were 60.34%, and 68.27%, lower than those of the control, respectively;18.21,g/L acetic acid,33.42%, times higher than that of the control,accumulated in the broth.In conclusion,in shake flask fermentation assays,the metabolic flux of the recombined strain was beneficial forL-tryptophan accumulation although the biomass was lower thanE.coli TRTH.On the contrary,enhancement of glyoxylate shunt resulted in the short-age of energy supply and higher acetic acid accumulation,which can lead to lower biomass andL-tryptophan titer in 30,L fermentation.

关键词

L-色氨酸/大肠杆菌/乙醛酸循环/iclR/发酵

Key words

L-tryptophan/Escherichia coli/glyoxylate shunt/iclR/fermentation

分类

生物科学

引用本文复制引用

陈胜杰,刘辉,谢希贤,徐庆阳,陈宁..敲除iclR基因对大肠杆菌发酵L-色氨酸的影响[J].天津科技大学学报,2016,31(3):25-30,6.

基金项目

国家高技术研究发展计划资助项目(2012AA022102,2012AA02A703);天津市科技支撑计划重点资助项目(14ZCZDSY00015) (2012AA022102,2012AA02A703)

天津科技大学学报

OA北大核心CSTPCD

1672-6510

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