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活细菌中的基因编码化学脱笼

Genetically Encoded Chemical Decaging in Living Bacteria.

作者信息

Liu Lu, Liu Yanjun, Zhang Gong, Ge Yun, Fan Xinyuan, Lin Feng, Wang Jie, Zheng Huangtao, Xie Xiao, Zeng Xiangmei, Chen Peng R

机构信息

Beijing National Laboratory for Molecular Sciences, Synthetic and Functional Biomolecules Center, Department of Chemical Biology, College of Chemistry and Molecular Engineering, Peking University , Beijing 100871, China.

Peking-Tsinghua Center for Life Sciences , Beijing 100871, China.

出版信息

Biochemistry. 2018 Jan 30;57(4):446-450. doi: 10.1021/acs.biochem.7b01017. Epub 2017 Nov 29.

Abstract

We report the genetically encoded chemical decaging strategy for protein activation in living bacterial cells. In contrast to the metabolically labile photocaging groups inside Escherichia coli, our chemical decaging strategy that relies on the inverse electron-demand Diels-Alder (iDA) reaction is compatible with the intracellular environment of bacteria, which can be a general tool for gain-of-function study of a given protein in prokaryotic systems. By applying this strategy for in situ activation of the indole-producing enzyme TnaA, we built an orthogonal and chemically inducible indole production pathway inside E. coli cells, which revealed the role of indole in bacterial antibiotic tolerance.

摘要

我们报道了用于活细菌细胞中蛋白质激活的基因编码化学脱笼策略。与大肠杆菌内部代谢不稳定的光笼基团不同,我们基于逆电子需求狄尔斯-阿尔德(iDA)反应的化学脱笼策略与细菌的细胞内环境兼容,这可以作为原核系统中特定蛋白质功能获得性研究的通用工具。通过应用该策略原位激活吲哚生成酶TnaA,我们在大肠杆菌细胞内构建了一条正交且化学诱导的吲哚生成途径,揭示了吲哚在细菌抗生素耐受性中的作用。

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