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膦酸盐的广泛水解:已知组氨酸 6 位有机磷水解酶的意外行为。

Extensive hydrolysis of phosphonates as unexpected behaviour of the known His6-organophosphorus hydrolase.

机构信息

Chemistry Department, Lomonosov Moscow State University, Lenin Hills, 1, building 3, Moscow, 119991, Russia.

Institute of Biochemical Physics RAS, Kosygin St. 4, Moscow, 119334, Russia.

出版信息

Appl Microbiol Biotechnol. 2016 Jul;100(13):5829-38. doi: 10.1007/s00253-016-7407-x. Epub 2016 Mar 2.

Abstract

The catalytic activity of hexahistidine-tagged organophosphorus hydrolase (His6-OPH) in hydrolytic reactions of methylphosphonic acid (MPA) and its monoesters and diesters being decomposition products of R-VX was demonstrated for the first time. The catalytic constants of enzyme in such reactions were determined. The mechanism of C-P bond cleavage in the MPA by His6-OPH was proposed. Such reaction was estimated to be carried out with the soluble and nanocapsulated forms of His6-OPH. His6-OPH was demonstrated to be capable of degrading the key organophosphorus components of reaction masses (RMs) that are produced by the chemical detoxification of R-VX and RMs are multi-substrate mixtures for this enzyme. The kinetic model describing the behaviour of His6-OPH in RMs was proposed and was shown to adequately fit experimental points during degradation of the real samples of RMs.

摘要

首次证明了六组氨酸标签的有机磷水解酶(His6-OPH)在甲基膦酸(MPA)及其单酯和二酯(VX 反应的分解产物)水解反应中的催化活性。确定了酶在这些反应中的催化常数。提出了 His6-OPH 催化 MPA 中 C-P 键断裂的机制。据估计,这种反应是通过 His6-OPH 的可溶性和纳米胶囊形式进行的。证明 His6-OPH 能够降解由 VX 和反应混合物(RMs)的化学解毒产生的反应混合物(RMs)中的关键有机磷成分,而 RMs 是该酶的多底物混合物。提出了描述 His6-OPH 在 RMs 中行为的动力学模型,并在降解真实的 RMs 样品时,实验点与模型拟合良好。

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