Disruption of the acetoacetate decarboxylase gene in solvent-producing Clostridium acetobutylicum increases the butanol ratio

被引:176
作者
Jiang, Yu [1 ,2 ]
Xu, Chongmao [1 ,2 ]
Dong, Feng [1 ,2 ]
Yang, Yunliu [1 ]
Jiang, Weihong [1 ,2 ]
Yang, Sheng [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Plant Physiol & Ecol, Key Lab Synthet Biol, Shanghai 200032, Peoples R China
[2] Shanghai Res & Dev Ctr Ind Biotechnol, Shanghai 201201, Peoples R China
[3] Chinese Acad Sci, Huzhou Ctr Ind Biotechnol, Shanghai Inst Biol Sci, Huzhou 313000, Peoples R China
基金
中国国家自然科学基金;
关键词
Acetone; Acetoacetic acid decarboxylase; Butanol ratio; Clostridium acetobutylicum; Gene disruption; ENHANCED BUTYRIC-ACID; ESCHERICHIA-COLI; DOWN-REGULATION; ATCC; 824; ACETONE FORMATION; ETHANOL FERMENTATION; HYDROGEN-PRODUCTION; NADH AVAILABILITY; COA-TRANSFERASE; CARBON-MONOXIDE;
D O I
10.1016/j.ymben.2009.06.002
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
A possible way to improve the economic efficacy of acetone-butanol-ethanol fermentation is to increase the butanol ratio by eliminating the production of other by-products, such as acetone. The acetoacetate decarboxylase gene (adc) in the hyperbutanol-producing industrial strain Clostridium acetobutylicum EA 2018 was disrupted using TargeTron technology. The butanol ratio increased from 70% to 80.05%, with acetone production reduced to approximately 0.21 g/L in the adc-disrupted mutant (2018adc). pH control was a critical factor in the improvement of cell growth and solvent production in strain 2018adc. The regulation of electron flow by the addition of methyl viologen altered the carbon flux from acetic acid production to butanol production in strain 2018adc, which resulted in an increased butanol ratio of 82% and a corresponding improvement in the overall yield of butanol from 57% to 70.8%. This study presents a general method of blocking acetone production by Clostridium and demonstrates the industrial potential of strain 2018adc. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:284 / 291
页数:8
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