吉林大学学报(理学版)

• 生命科学 • 上一篇    下一篇

大肠杆菌丁醇生产菌的构建及检测

李晓丹, 姬艳丽, 吴日, 屠培培, 段会坤,尼再中, 王海松, 李淼, 姜苹哲, 李明刚   

  1. 南开大学 教育部活性材料重点实验室, 生命科学学院, 天津 300071
  • 收稿日期:2015-05-28 出版日期:2016-03-26 发布日期:2016-03-23
  • 通讯作者: 李明刚 E-mail:mgl@nankai.edu.cn

Construction of Butanol Generating E.coli and Its Identification

LI Xiaodan, JI Yanli, WU Ri, TU Peipei, DUAN Huikun,NI Zaizhong, WANG Haisong, LI Miao, JIANG Pingzhe, LI Minggang   

  1. College of Life Science, Key Laboratory for Bioactive Materials of the Ministry of Education,Nankai University, Tianjin 300071, China
  • Received:2015-05-28 Online:2016-03-26 Published:2016-03-23
  • Contact: LI Minggang E-mail:mgl@nankai.edu.cn

摘要:

用合成生物学和代谢工程技术, 筛选并克隆丁醇合成途径中酶活性较高的atoB,hbd,crt,ter,adhE2等5个关键酶基因, 先通过重组PCR构建pUC18-atoB-hbd-crtter质粒, 再将串联基因atoB-hbd-crt-ter和基因adhE2克隆至质粒pET-21b中, 构建含丁醇合成途径的表达载体pET-21b-atoB-hbd-crt-teradhE2, 将其转入大肠杆菌E.coli BL21(DE3)中制备工程菌株. 对样品进行IPTG诱导表达检测与色谱分析的结果表明, 已合成出关键酶蛋白并产生一定量的丁醇.

关键词: 大肠杆菌, 生物燃料, 丁醇, 发酵

Abstract:

Using synthetic biology and metabolic engineering techniques, we screened and cloned 5 key enzyme gene atoB,hbd,crt,adhE2 and ter with relatively high activity in butanol synthesis pathway. Firstly, we constructed the pUC18-atoB-hbd-crt-ter plasmid by recombinant PCR, and then coloned tandem gene atoB-hbd-crt-ter and gene adhE2 into the plasmid pET21b and eventually constructed the expression vector of pET-21b-atoB-hbd-crt-ter-adhE2 containing butanol synthesis pathway, and transferred it into E.coli BL21 (DE3) for the preparation of engineering strains. We performed IPTG induced expression detection and gas chromatograph (GC) analysis of samples. The results show that key enzyme proteins have been synthesized and produced a certain amount of butanol.

Key words: escherichia coli (E.coli), biofuels, butanol, fermentation

中图分类号: 

  • Q819