Engineering of cofactor regeneration enhances (2S,3S)-2,3-butanediol production from diacetyl

被引:65
作者
Wang, Yu [1 ,2 ,3 ]
Li, Lixiang [1 ,2 ,3 ]
Ma, Cuiqing [3 ]
Gao, Chao [3 ]
Tao, Fei [1 ,2 ]
Xu, Ping [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, State Key Lab Microbial Metab, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Shanghai 200240, Peoples R China
[3] Shandong Univ, State Key Lab Microbial Technol, Jinan 250100, Peoples R China
来源
SCIENTIFIC REPORTS | 2013年 / 3卷
基金
中国国家自然科学基金;
关键词
BIOCATALYTIC KETONE REDUCTION; ESCHERICHIA-COLI; CHIRAL ALCOHOLS; POWERFUL TOOL; 2,3-BUTANEDIOL; FERMENTATION; EXPRESSION; MANNITOL; GLUCOSE; PATHWAY;
D O I
10.1038/srep02643
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
(2S,3S)-2,3-Butanediol ((2S,3S)-2,3-BD) is a potentially valuable liquid fuel and an excellent building block in asymmetric synthesis. In this study, cofactor engineering was applied to improve the efficiency of (2S, 3S)-2,3-BD production and simplify the product purification. Two NADH regeneration enzymes, glucose dehydrogenase and formate dehydrogenase (FDH), were introduced into Escherichia coli with 2,3-BD dehydrogenase, respectively. Introduction of FDH resulted in higher (2S, 3S)-2,3-BD concentration, productivity and yield from diacetyl, and large increase in the intracellular NADH concentration. In fed-batch bioconversion, the final titer, productivity and yield of (2S, 3S)-2,3-BD on diacetyl reached 31.7 g/L, 2.3 g/(L.h) and 89.8%, the highest level of (2S, 3S)-2,3-BD production thus far. Moreover, cosubstrate formate was almost totally converted to carbon dioxide and no organic acids were produced. The biocatalytic process presented should be a promising route for biotechnological production of NADH-dependent microbial metabolites.
引用
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页数:6
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