In silico design and adaptive evolution of Escherichia coli for production of lactic acid

被引:258
作者
Fong, SS
Burgard, AP
Herring, CD
Knight, EM
Blattner, FR
Maranas, CD
Palsson, BO
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[2] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[3] Univ Wisconsin, Dept Genet, Madison, WI 53706 USA
关键词
computational model; metabolic engineering; evolution; Escherichia coli;
D O I
10.1002/bit.20542
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
The development and validation of new methods to help direct rational strain design for metabolite overproduction remains an important problem in metabolic engineering. Here we show that computationally predicted E. coli strain designs, calculated from a genome-scale metabolic model, can lead to successful production strains and that adaptive evolution of the engineered strains can lead to improved production capabilities. Three strain designs for lactate production were implemented yielding a total of 11 evolved production strains that were used to demonstrate the utility of this integrated approach. Strains grown on 2 g/L glucose at 37 degrees C showed lactate titers ranging from 0.87 to 1.75 g/L and secretion rates that were directly coupled to growth rates. (C) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:643 / 648
页数:6
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