The rebalanced pathway significantly enhances acetoin production by disruption of acetoin reductase gene and moderate-expression of a new water-forming NADH oxidase in Bacillus subtilis

被引:89
作者
Zhang, Xian [1 ]
Zhang, Rongzhen [1 ]
Bao, Teng [1 ]
Rao, Zhiming [1 ]
Yang, Taowei [1 ]
Xu, Meijuan [1 ]
Xu, Zhenghong [2 ]
Li, Huazhong [1 ]
Yang, Shangtian [3 ]
机构
[1] Jiangnan Univ, Sch Biotechnol, Minist Educ, Key Lab Ind Biotechnol, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Sch Med & Pharmaceut, Wuxi 214122, Jiangsu, Peoples R China
[3] Ohio State Univ, Dept Chem Engn, Columbus, OH 43210 USA
基金
中国国家自然科学基金;
关键词
Bacillus subtilis; Gene disruption; Acetoin reductase/2,3-butanediol; dehydrogenase; NADH oxidase; Acetoin pathway; METABOLIC FLUX REDISTRIBUTION; SERRATIA-MARCESCENS H32; LACTOCOCCUS-LACTIS; STATISTICAL OPTIMIZATION; ESCHERICHIA-COLI; 2,3-BUTANEDIOL; DEHYDROGENASE; DIACETYL; OVEREXPRESSION; PURIFICATION;
D O I
10.1016/j.ymben.2014.02.002
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
Bacillus sub tills produces acetoin as a major extracellular product. However, the by-products of 2,3-butanediol, lactic acid and ethanol were accompanied in the NADH-dependent pathways. In this work, metabolic engineering strategies were proposed to redistribute the carbon flux to acetoin by manipulation the NADH levels. We first knocked out the acetoin reductase gene bdhA to block the main flux from acetoin to 2,3-butanediol. Then, among four putative candidates, we successfully screened an active water forming NADH oxidase, YODC. Moderate expression of YODC in the bdhA disrupted B. subtilis weakened the NADH-linked pathways to by-product pools of acetoin. Through these strategies, acetoin production was improved to 56.7 g/l with an increase of 35.3%, while the production of 2,3-butanediol, lactic acid and ethanol were decreased by 92.3%, 70.1% and 75.0%, respectively, simultaneously the fermentation duration was decreased 1.7-fold. Acetoin productivity by B. subtilis was improved to 0.639 g/(1h). (C) 2014 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:34 / 41
页数:8
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