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利用不相容质粒系统通过重组大肠杆菌从甘油生产1,3 - 丙二醇。

Production of 1,3-propanediol from glycerol by recombinant E. coli using incompatible plasmids system.

作者信息

Wang Fenghuan, Qu Huijin, Zhang Dawei, Tian Pingfang, Tan Tianwei

机构信息

Beijing Key Lab of Bioprocess, College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.

出版信息

Mol Biotechnol. 2007 Oct;37(2):112-9. doi: 10.1007/s12033-007-0041-1.

Abstract

1,3-Propanediol (1,3-PD) has numerous applications in polymers, cosmetics, foods, lubricants, and medicines as a bifunctional organic compound. The genes for the production of 1,3-PD in Klebsiella pneumoniae, dhaB, which encodes glycerol dehydratase, and dhaT, which encodes 1,3-PD oxidoreductase, and gdrAB, which encodes glycerol dehydratase reactivating factor, are naturally under the control of different promoters and are transcribed in different directions. These genes were coexpressed in E. coli using two incompatible plasmids (pET28a and pET22b) in the presence of selective pressure. The recombinant E. coli coexpressed the glycerol dehydratase, 1,3-propanediol oxidoreductase and reactivating factor for the glycerol dehydratase at high levels. In a fed-batch fermentation of glycerol and glucose, the recombinant E. coli containing these two incompatible plasmids consumed 14.3 g/l glycerol and produced 8.6 g/l 1,3-propanediol. In the substitution case of yqhD (encoding alcohol dehydrogenase from E. coli) for dhaT, the final 1,3-propanediol concentration of the recombinant E. coli could reach 13.2 g/l.

摘要

1,3 - 丙二醇(1,3 - PD)作为一种双功能有机化合物,在聚合物、化妆品、食品、润滑剂和药品等领域有众多应用。肺炎克雷伯菌中负责生产1,3 - PD的基因,即编码甘油脱水酶的dhaB、编码1,3 - 丙二醇氧化还原酶的dhaT以及编码甘油脱水酶再激活因子的gdrAB,天然情况下受不同启动子控制且转录方向不同。在选择性压力存在的情况下,利用两个不相容质粒(pET28a和pET22b)在大肠杆菌中共表达这些基因。重组大肠杆菌高水平共表达了甘油脱水酶、1,3 - 丙二醇氧化还原酶以及甘油脱水酶的再激活因子。在甘油和葡萄糖的补料分批发酵中,含有这两个不相容质粒的重组大肠杆菌消耗了14.3 g/L甘油,产生了8.6 g/L 1,3 - 丙二醇。在用yqhD(编码来自大肠杆菌的乙醇脱氢酶)替换dhaT的情况下,重组大肠杆菌的最终1,3 - 丙二醇浓度可达13.2 g/L。

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