Refactoring redox cofactor regeneration for high-yield biocatalysis of glucose to butyric acid in Escherichia coli

被引:33
|
作者
Lim, Jae Hyung [1 ]
Seo, Sang Woo [2 ]
Kim, Se Yeon [1 ]
Jung, Gyoo Yeol [1 ,2 ]
机构
[1] Pohang Univ Sci & Technol, Sch Interdisciplinary Biosci & Bioengn, Pohang 790784, Gyeongbuk, South Korea
[2] Pohang Univ Sci & Technol, Dept Chem Engn, Pohang 790784, Gyeongbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Biocatalysis; Cofactor regeneration; Butyric acid; Synthetic biology; Fermentation; CLOSTRIDIUM-TYROBUTYRICUM; HYDROGEN-PRODUCTION; THIOESTERASE-II; DELETED MUTANT; K-12; MUTANT; GENES; CONSTRUCTION; FERMENTATION; PATHWAYS; ACETOBUTYLICUM;
D O I
10.1016/j.biortech.2012.09.091
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
In this study, the native redox cofactor regeneration system in Escherichia coli was engineered for the production of butyric acid. The synthetic butyrate pathway, which regenerates NAD(+) from NADH using butyrate as the only final electron acceptor, enabled high-yield production of butyric acid from glucose (83.4% of the molar theoretical yield). The high selectivity for butyrate, with a butyrate/acetate ratio of 41, suggests dramatically improved industrial potential for the production of butyric acid from nonnative hosts compared to the native producers (Clostridium species). Furthermore, this strategy could be broadly utilized for the production of various other useful chemicals in the fields of metabolic engineering and synthetic biology. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:568 / 573
页数:6
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