大肠杆菌
代谢工程
起始密码子
2,3-丁二醇
化学
密码子使用偏好性
生物化学
基因
转移RNA
生物
食品科学
信使核糖核酸
发酵
基因组
核糖核酸
作者
Seo‐Young Park,Borim Kim,Soojin Lee,Min‐Kyu Oh,Jong‐In Won,Jinwon Lee
摘要
The natural microorganism Escherichia coli without modification is not suitable for the efficient production of 2,3-butanediol (2,3-BD) on an industrial scale because of its poor metabolic performance. Metabolic capacities of E. coli have been improved to produce 2,3-BD efficiently, the performance of which is possible for producing such a product. Codon optimization with the ribosome-binding site for the efficient production of target genes (budA and budC) was achieved by molecular engineering, which allowed the metabolic engineering to proceed to the next level. As a result, comparing the productivity in 26 H, where the amount of p18COR was 1.04 g/L and that of p18WTR was 0.41 g/L, represents an approximate 60.6% increase in the productivity of the p18WTR with codon optimization. In other words, p18COR was 2.54-fold greater than p18WTR in the production of 2,3-BD.
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