大肠杆菌
单元格排序
色氨酸
拉伤
突变
高通量筛选
生物传感器
生产过剩
生物
基因
计算生物学
突变体
遗传学
氨基酸
化学
生物化学
细胞
解剖
作者
Yongfei Liu,Huiling Yuan,Dongqin Ding,Huina Dong,Qinhong Wang,Dawei Zhang
标识
DOI:10.1021/acssynbio.0c00647
摘要
With the flexibility to fold into complex structures, RNA is well-suited to act as a cellular sensor to recognize environmental fluctuations and respond to changes by regulating the corresponding genes. In this study, we established a high-throughput screening platform to screen tryptophan high-producing strains from a large repertoire of candidate strains. This platform consists of a tryptophan-specific aptamer-based biosensor and fluorescence-activated droplet sorting technology. One mutant strain, with a 165.9% increase in Trp titer compared with the parental strain, was successfully screened from a random mutagenesis library. Sequencing results revealed that a total of 10 single-nucleotide polymorphisms were discovered in the genome of the mutant strain, among which CRP(T29K) was proven to significantly increase Trp production through improving the strain's tolerance of the harsh environment during the stationary phase of the fermentation process. Our results indicate that this strategy has great potential for improving the production of other amino acids in Escherichia coli.
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