Fed-Batch Culture of Escherichia coli for L-Valine Production Based on In Silico Flux Response Analysis

被引:65
作者
Park, Jin Hwan [1 ,2 ,3 ]
Kim, Tae Yong [1 ,2 ,3 ]
Lee, Kwang Ho [1 ]
Lee, Sang Yup [1 ,2 ,3 ,4 ,5 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Program BK21, Metab & Biomol Engn Natl Res Lab, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, Inst BioCentury, Ctr Syst & Synthet Biotechnol, Taejon 305701, South Korea
[3] Korea Adv Inst Sci & Technol, BioProc Engn Res Ctr, Taejon 305701, South Korea
[4] Korea Adv Inst Sci & Technol, Bioinformat Res Ctr, Dept Bio & Brain Engn, Taejon 305701, South Korea
[5] Korea Adv Inst Sci & Technol, Bioinformat Res Ctr, Dept Biol Sci, Taejon 305701, South Korea
关键词
L-valine; fed-batch culture; in silico flux response analysis; systems metabolic engineering; CORYNEBACTERIUM-GLUTAMICUM; K-12; GENE; GROWTH; MUTANT;
D O I
10.1002/bit.22995
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
We have previously reported the development of a 100% genetically defined engineered Escherichia coli strain capable of producing L-valine from glucose with a high yield of 0.38 g L-valine per gram glucose (0.58 mol L-valine per mol glucose) by batch culture. Here we report a systems biological strategy of employing flux response analysis in bioprocess development using L-valine production by fed-batch culture as an example. Through the systems-level analysis, the source of ATP was found to be important for efficient L-valine production. There existed a trade-off between L-valine production and biomass formation, which was optimized for the most efficient L-valine production. Furthermore, acetic acid feeding strategy was optimized based on flux response analysis. The final fed-batch cultivation strategy allowed production of 32.3 g/L L-valine, the highest concentration reported for E. coli. This approach of employing systems-level analysis of metabolic fluxes in developing fed-batch cultivation strategy would also be applicable in developing strategies for the efficient production of other bioproducts. Biotechnol. Bioeng. 2011;108: 934-946. (C) 2010 Wiley Periodicals, Inc.
引用
收藏
页码:934 / 946
页数:13
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