Genetic manipulation of Escherichia coli central carbon metabolism for efficient production of fumaric acid

被引:24
作者
Liu, Huan [1 ]
Song, Ruirui [2 ]
Liang, Yue [1 ]
Zhang, Ting [3 ]
Deng, Li [1 ]
Wang, Fang [1 ]
Tan, Tianwei [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn Beijing, Beijing Bioproc Key Lab, Beijing 100029, Peoples R China
[2] China Natl Inst Standardizat, Inst Food & Agr Standardizat, Beijing 100191, Peoples R China
[3] 302 Hosp PLA, Comprehens Liver Canc Ctr, Beijing 100039, Peoples R China
关键词
Fumaric acid; Malic acid; Acetic acid; Escherichia coli; Phosphate-transferase system; ARRHIZUS RH 7-13-9-POUND; RHIZOPUS-ARRHIZUS; MALATE PRODUCTION; FERMENTATION; PATHWAYS; GLYCEROL; XYLOSE;
D O I
10.1016/j.biortech.2018.08.024
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Fumaric acid is one of the top 12-biomass building-block chemicals. In this study, we reported manipulation of E. coli central carbon metabolism with the aim to decrease the by-products and improve fumaric acid production. PEP-dependent glucose phosphotransferase system was replaced with a galactose translocation system to minimize the consumption of phosphoenolpyruvate. Engineering anaplerotic pathway (phosphoenolpyruvate carboxylase) was employed to redistribute carbon flux from glycolysis to Krebs cycle. Deletion of malate dehydrogenase and overexpression of acetyl-CoA synthase could decrease the byproducts malic acid and acetic acid. The combined strategies led to fumaric acid yield up to 1.53 g/g dry cell weight, a 50% increase compared with the parental strain. The result demonstrated that these genetic modifications were effective strategies for improving the production of fumaric acid and the engineered strain may serve a platform microbial cell factory for efficient production of fumaric acid or other dicarboxylic acids.
引用
收藏
页码:96 / 102
页数:7
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