硝基还原酶
硝基
细胞外
化学
细菌
细胞内
荧光
分子内力
生物物理学
分子
电子转移
生物化学
立体化学
组合化学
光化学
生物
酶
有机化学
物理
烷基
量子力学
遗传学
作者
Shu-Xia Jiang,Le Xu,Yihong Zhong,Chuangchuang Zhang,Xiaoyu Yu,Ke Li,Lin Ding,Xiaojian Wang
标识
DOI:10.1002/cbic.202400257
摘要
Nitroreductase (NTR) has long been a target of interest for its important role involved in the nitro compounds metabolism. Various probes have been reported for NTR analysis, but rarely able to distinguish the extracellular NTR from intracellular ones. Herein we reported a new NTR sensor, HCyS‐NO2, which was a hemicyanine molecule with one nitro and two sulfo groups attached. The nitro group acted as the reporting group to respond NTR reduction. Direct linkage of nitro group into the hemicyanine π conjugate system facilitated the intramolecular electron transfer (IET) process and thus quenched the fluorescence of hemicyanine core. Upon reduction with NTR, the nitro group was rapidly converted into the hydroxylamino and then the amino group, eliminating IET process and thus restoring the fluorescence. The sulfo groups installed significantly increased the hydrophilicity of the molecule, and introduced negative charges at physiological pH, preventing the diffusion into bacteria. Both gram‐negative and gram‐positive bacteria were able to turn on the fluorescence of HCyS‐NO2, without detectable diffusion into cells, providing a useful tool to probe the extracellular reduction process.
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