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新型TdsD硝基还原酶:动力学和底物特异性表征

Novel TdsD nitroreductase: characterization of kinetics and substrate specificity.

作者信息

Valiauga Benjaminas, Žulpaitė Dovydė, Sharrock Abigail V, Ackerley David F, Čėnas Narimantas

机构信息

Institute of Biochemistry of Vilnius University, Saulėtekio 7, 10257, Vilnius, Lithuania.

School of Biological Sciences, Victoria University of Wellington, Kelburn Parade, Wellington, 6140, New Zealand.

出版信息

Biotechnol Lett. 2025 Sep 12;47(5):103. doi: 10.1007/s10529-025-03636-x.

Abstract

The reduction of quinones and nitroaromatic compounds catalyzed by Type I nitroreductases is important due to its role in their potential cytotoxic effects and/or biodegradation. The main goal of this work was to investigate the mechanism of catalysis of a TdsD nitroreductase (NR) (TdsD1), a member from an understudied branch of the nitroreductase superfamily, derived from a soil metagenome study. Like the Type I NRs NfsA and NfsB, TdsD1 performed two-electron reduction of quinones and four-electron reduction of nitroaromatic compounds according to a "ping-pong" mechanism with a rate-limiting oxidative half-reaction. TdsD1 was also inhibited by the classical inhibitors of other NRs, dicoumarol and Cibacron blue. Despite sharing only a low degree of homology with the NfsA and NfsB subfamily enzymes, sequence comparisons and computer modelling point to the possibility of an analogous FMN isoalloxazine ring location within the intersubunit space of TdsD1. It also possesses similar specificity for nitroaromatic compounds and quinones, in particular the shared characteristic of being especially active with 2-hydroxy-1,4-naphthoquinone derivatives. It is possible that the similar character of binding of oxidants and other ligands relative to the NfsA and NfsB subfamily enzymes may be related to the conserved Arg27 and Ser53 residues in the active site of TdsD1.

摘要

I型硝基还原酶催化醌类和硝基芳香族化合物的还原反应具有重要意义,因为这一反应在其潜在的细胞毒性效应和/或生物降解过程中发挥着作用。本研究的主要目的是探究一种TdsD硝基还原酶(NR)(TdsD1)的催化机制,该酶来自硝基还原酶超家族中一个研究较少的分支,是通过土壤宏基因组研究获得的。与I型NRs的NfsA和NfsB一样,TdsD1按照“乒乓”机制对醌类进行双电子还原,对硝基芳香族化合物进行四电子还原,氧化半反应为限速步骤。TdsD1也受到其他NRs的经典抑制剂双香豆素和汽巴克隆蓝的抑制。尽管与NfsA和NfsB亚家族酶的同源性较低,但序列比较和计算机建模表明,TdsD1亚基间空间内可能存在类似的FMN异咯嗪环位置。它对硝基芳香族化合物和醌类也具有相似的特异性,特别是对2-羟基-1,4-萘醌衍生物具有特别高的活性这一共同特征。相对于NfsA和NfsB亚家族酶,TdsD1与氧化剂和其他配体的结合特性相似,这可能与TdsD1活性位点中保守的Arg27和Ser53残基有关。

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