详细信息

Over-expression of glycerol dehydrogenase and 1,3-propanediol oxidoreductase in Klebsiella pneumoniae and their effects on conversion of glycerol into 1,3-propanediol in resting cell system  ( SCI-EXPANDED收录)  

文献类型:期刊文献

英文题名:Over-expression of glycerol dehydrogenase and 1,3-propanediol oxidoreductase in Klebsiella pneumoniae and their effects on conversion of glycerol into 1,3-propanediol in resting cell system

作者:Zhao, Li[1];Ma, Xingyuan[1];Zheng, Yu[1];Zhang, Jianguo[1];Wei, Guodong[1];Wei, Dongzhi[1]

机构:[1]E China Univ Sci & Technol, State Key Lab Bioreactor Engn, New World Inst Biotechnol, Shanghai 200237, Peoples R China

年份:2009

卷号:84

期号:4

起止页码:626

外文期刊名:JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY

收录:;WOS:【SCI-EXPANDED(收录号:WOS:000264946500023)】;

基金:This work was supported by the National Special Fund for State Key Laboratory of Bioreactor Engineering, Grant No. 2060204.

语种:英文

外文关键词:1,3-propanediol; 1,3-propanediol oxidoreductase; glycerol dehydrogenase; resting cell system; Klebsiella pneumoniae

摘要:BACKGROUND: Glycerol dehydrogenase [EC.1.1.1.6] and 1,3-propanediol oxidoreductase [EC.1.1.1.202] were proved to be two of the key enzymes for glycerol conversion to 1,3-propanediol in Klebsiella pneumoniae under anaerobic conditions. For insight into their significance on 1,3-propanediol production under micro-aerobic conditions, these two enzymes were over-expressed in K. pneumoniae individually, and their effects on conversion of glycerol into 1,3-propanediol in a resting cell system under micro-aerobic conditions were investigated. RESULTS: In the resting cell system, over-expression of 1,3-propanediol oxidoreductase led to faster glycerol conversion and 1,3-propanediol production. After a 12 h conversion process, it improved the yield of 1,3-propanediol by 20.4% (222.1 mmol L-1 versus 184.4 mmol L-1) and enhanced the conversion ratio of glycerol into 1,3-propanediol from 50.8% to 59.8% (mol mol(-1)). Over-expression of glycerol dehydrogenase in K. pneumoniae had no significant influence both on 1,3-propanediol yield and on the conversion ratio of glycerol into 1,3-propanediol in the resting cell system. CONCLUSION: The results were important for an understanding of the significance of glycerol dehydrogenase and 1,3-propanediol oxidoreductase in 1,3-proanediol production under micro-aerobic conditions, and for developing better strategies to improve 1,3-propanediol yield. (c) 2008 Society of Chemical Industry

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