Engineering of NADPH regenerators in Escherichia coli for enhanced biotransformation

被引:91
作者
Lee, Won-Heong [1 ,2 ,3 ,4 ]
Kim, Myoung-Dong [5 ]
Jin, Yong-Su [3 ,4 ]
Seo, Jin-Ho [1 ,2 ]
机构
[1] Seoul Natl Univ, Dept Agr Biotechnol, Seoul 151921, South Korea
[2] Seoul Natl Univ, Ctr Food & Bioconvergence, Seoul 151921, South Korea
[3] Univ Illinois, Dept Food Sci & Human Nutr, Urbana, IL 61801 USA
[4] Univ Illinois, Inst Genom Biol, Urbana, IL 61801 USA
[5] Kangwon Natl Univ, Dept Food Sci & Biotechnol, Chunchon 200701, South Korea
基金
新加坡国家研究基金会;
关键词
Biotransformation process; Engineered Escherichia coli; NADPH regeneration; Pentose phosphate; PYRIDINE-NUCLEOTIDE TRANSHYDROGENASE; WHOLE-CELL BIOCATALYSIS; DEPENDENT MALIC ENZYME; ALCOHOL-DEHYDROGENASE; OVEREXPRESSION; BIOSYNTHESIS; EXPRESSION; GENE; UDHA; METABOLISM;
D O I
10.1007/s00253-013-4750-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Efficient regeneration of NADPH is one of the limiting factors that constrain the productivity of biotransformation processes. In order to increase the availability of NADPH for enhanced biotransformation by engineered Escherichia coli, modulation of the pentose phosphate pathway and amplification of the transhydrogenases system have been conventionally attempted as primary solutions. Recently, other approaches for stimulating NADPH regeneration during glycolysis, such as replacement of native glyceradehdye-3-phosphate dehydrogenase (GAPDH) with NADP-dependent GAPDH from Clostridium acetobutylicum and introduction of NADH kinase catalyzing direct phosphorylation of NADH to NADPH from Saccharomyces cerevisiae, were attempted and resulted in remarkable impacts on NADPH-dependent bioprocesses. This review summarizes several metabolic engineering approaches used for improving the NADPH regenerating capacity in engineered E. coli for whole-cell-based bioprocesses and discusses the key features and progress of those attempts.
引用
收藏
页码:2761 / 2772
页数:12
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