氨基酸
生物化学
突变体
定向进化
遗传密码
蛋白质工程
无细胞蛋白质合成
合成生物学
代谢工程
周质间隙
蛋白质生物合成
生物
大肠杆菌
绿色荧光蛋白
化学
细菌蛋白
荧光蛋白
功能(生物学)
基因工程
工业微生物学
计算生物学
定向分子进化
细菌
遗传筛选
基因
化学基因学
转移RNA
细胞
氨酰tRNA合成酶
转基因生物
蛋白质标签
蛋白质功能
突变蛋白
克隆(编程)
作者
Wooseok Ko,Rahul Kumar,Sanggil Kim,Hyun Soo Lee
标识
DOI:10.1021/acssynbio.9b00076
摘要
Engineered organisms with an expanded genetic code have attracted much attention in chemical and synthetic biology research. In this work, engineered bacterial organisms with enhanced unnatural amino acid (UAA) uptake abilities were developed by screening periplasmic binding protein (PBP) mutants for recognition of UAAs. A FRET-based assay was used to identify a mutant PBP (LBP-AEL) with excellent binding affinity ( Kd ≈ 500 nM) to multiple UAAs from 37 mutants. Bacterial cells expressing LBP-AEL showed up to 5-fold enhanced uptake of UAAs, which was determined by genetic incorporation of UAAs into a green fluorescent protein and measuring UAA concentration in cell lysates. To the best of our knowledge, this work is the first report of engineering cellular uptake of UAAs and could provide an impetus for designing advanced unnatural organisms with an expanded genetic code, which function with the efficiency comparable to that of natural organisms. The system would be useful to increase mutant protein yield from lower concentrations of UAAs for industrial and large-scale applications. In addition, the techniques used in this report such as the sensor design and the measurement of UAA concentration in cell lysates could be useful for other biochemical applications.
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