化学
突变体
定向进化
生物化学
体内
催化作用
基质(水族馆)
蛋白质工程
生物合成
色氨酸
ATP合酶
产量(工程)
细胞
效价
酶
组合化学
细胞生物学
分子内力
单元格排序
代谢工程
细胞培养
生物物理学
底物特异性
色氨酸合酶
作者
Xingyu Zhu,Hengwei Zhang,Di Zhang,Jin Han,Liangyuchuan Fang,Yanan Li,Jiajia You,Zhiming Rao
标识
DOI:10.1021/acs.jafc.6c00815
摘要
In recent years, the direct synthesis of l-cysteine from l-serine and sodium hydrosulfide catalyzed by tryptophan synthase (TrpS) has attracted considerable attention. However, under high substrate concentration conditions, the conversion efficiency of TrpS remains limited, which restricts its industrial application. To enhance catalytic efficiency, this study developed a directed evolution platform integrating in vivo continuous mutagenesis, a highly sensitive l-cysteine biosensor, and fluorescence-activated cell sorting for high-throughput screening. Using this platform, multiple TrpS variants were successfully obtained, among which the combinatorial mutant V139M/A302P exhibited superior catalytic activity and stability compared with the wild type. Under optimized reaction conditions, this mutant achieved an l-cysteine titer of 116.4 g/L. Furthermore, by introducing a whole-cell immobilization strategy, the immobilized cells produced a maximum l-cysteine titer of 113.05 g/L in a single batch, with a conversion rate of 93.3%. This study establishes an efficient, stable, and industrially promising platform for l-cysteine biosynthesis and screening.
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