谷氨酸棒杆菌
代谢工程
合成生物学
大肠杆菌
基因敲除
生物化学
生物
转移RNA
核糖核酸
基因
计算生物学
化学
作者
Dehu Sun,Jiuzhou Chen,Yu Wang,Mingyue Li,Deming Rao,Yanmei Guo,Ning Chen,Ping Zheng,Jibin Sun,Yanhe Ma
标识
DOI:10.1007/s10295-018-02128-4
摘要
Corynebacterium glutamicum is an important platform strain that is wildly used in industrial production of amino acids and various other biochemicals. However, due to good genomic stability, C. glutamicum is more difficult to engineer than genetically tractable hosts. Herein, a synthetic small regulatory RNA (sRNA)-based gene knockdown strategy was developed for C. glutamicum. The RNA chaperone Hfq from Escherichia coli and a rationally designed sRNA consisting of the E. coli MicC scaffold and a target binding site were proven to be indispensable for repressing green fluorescent protein expression in C. glutamicum. The synthetic sRNA system was applied to improve glutamate production through knockdown of pyk, ldhA, and odhA, resulting almost a threefold increase in glutamate titer and yield. Gene transcription and enzyme activity were down-regulated by up to 80%. The synthetic sRNA system developed holds promise to accelerate C. glutamicum metabolic engineering for producing valuable chemicals and fuels.
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