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.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 11-25 |
| 页数 | 15 |
| 期刊 | Metabolic Engineering |
| 卷 | 78 |
| DOI | |
| 出版状态 | 已出版 - 7月 2023 |
学术指纹
探究 'A tRNA Modification-based strategy for Identifying amiNo acid Overproducers (AMINO)' 的科研主题。它们共同构成独一无二的学术指纹。引用此
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