氨基酸
氨基酰化
转移RNA
谷氨酸棒杆菌
生物化学
氨酰tRNA合成酶
生物
遗传密码
大肠杆菌
氨基酰基tRNA合成酶
化学
基因
核糖核酸
作者
Hao Guo,Ning Wang,Tingting Ding,Bo Zheng,Liwei Guo,Chaoyong Huang,Wuyuan Zhang,Lichao Sun,Xiaoyan Ma,Yi‐Xin Huo
标识
DOI:10.1016/j.ymben.2023.04.012
摘要
Amino acids have a multi-billion-dollar market with rising demand, prompting the development of high-performance microbial factories. However, a general screening strategy applicable to all proteinogenic and non-proteinogenic amino acids is still lacking. Modification of the critical structure of tRNA could decrease the aminoacylation level of tRNA catalyzed by aminoacyl-tRNA synthetases. Involved in a two-substrate sequential reaction, amino acids with increased concentration could elevate the reduced aminoacylation rate caused by specific tRNA modification. Here, we developed a selection system for overproducers of specific amino acids using corresponding engineered tRNAs and marker genes. As a proof-of-concept, overproducers of five amino acids such as L-tryptophan were screened out by growth-based and/or fluorescence-activated cell sorting (FACS)-based screening from random mutation libraries of Escherichia coli and Corynebacterium glutamicum, respectively. This study provided a universal strategy that could be applied to screen overproducers of proteinogenic and non-proteinogenic amino acids in amber-stop-codon-recoded or non-recoded hosts.
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