发酵
大肠杆菌
重组DNA
生物化学
化学
拉伤
代谢工程
微生物
蛋白质工程
酶
细菌
生物
基因
遗传学
解剖
作者
Yong Tao,Qiong Cheng,Alexander D. Kopatsis
标识
DOI:10.1007/978-1-61779-483-4_18
摘要
Escherichia coli is the most commonly used microorganism for production of recombinant proteins for different applications. Acetate accumulation during aerobic growth on glucose has significant negative impact on recombinant protein production in Escherichia coli. Various strategies, such as process and genetic approaches have been developed to limit acetate formation to increase the productivity of recombinant proteins. We developed a strategy to combine inactivation of pyruvate oxidase (poxB) and over-expression of acety-CoA synthetase (acs) in E. coli K strain for controlling acetate accumulation. A recombinant peptide was expressed and produced in the engineered strains with a very low acetate formation in a 10-L fermentation process.
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