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西班牙金雀花过氧化物酶的动力学遵循乒乓双底物机制,并受到底物的竞争性抑制。

Kinetics of Spanish broom peroxidase obeys a Ping-Pong Bi-Bi mechanism with competitive inhibition by substrates.

作者信息

Pérez Galende Patricia, Hidalgo Cuadrado Nazaret, Kostetsky Eduard Ya, Roig Manuel G, Villar Enrique, Shnyrov Valery L, Kennedy John F

机构信息

Centro de Investigación y Desarrollo Tecnológico del Agua (CIDTA), Universidad de Salamanca, 37007 Salamanca, Spain.

Instituto de Estudios Biofuncionales, Departamento de Química-Física II, Facultad de Farmacia, Universidad Complutense de Madrid, 28040 Madrid, Spain.

出版信息

Int J Biol Macromol. 2015 Nov;81:1005-11. doi: 10.1016/j.ijbiomac.2015.09.042. Epub 2015 Sep 28.

Abstract

In plants, adverse conditions often induce an increase in reactive oxygen species (ROS) such as hydrogen peroxide (H2O2). H2O2 is reduced to water, and thus becomes detoxified by enzymes such as Cytisus multiflorus peroxidase (CMP). Here, the steady-state kinetics of the H2O2-supported oxidation of different organic substrates by CMP was investigated. Analysis of the initial rates vs. H2O2 and reducing substrate concentrations proved to be consistent with a substrate-inhibited Ping-Pong Bi-Bi reaction mechanism. The phenomenological approach expresses the peroxidase Ping-Pong mechanism in the form of the Michaelis-Menten equation and affords an interpretation of the effects in terms of the kinetic parameters [Formula: see text] , [Formula: see text] , kcat, [Formula: see text] , [Formula: see text] and of the microscopic rate constants, k1 and k3, of the shared three-step catalytic cycle of peroxidases.

摘要

在植物中,不利条件常常会促使活性氧(ROS)如过氧化氢(H₂O₂)的增加。H₂O₂被还原为水,从而通过诸如多花金雀儿过氧化物酶(CMP)等酶进行解毒。在此,研究了CMP对不同有机底物进行H₂O₂支持的氧化反应的稳态动力学。对初始速率与H₂O₂及还原底物浓度的分析结果证明与底物抑制的乒乓双底物反应机制一致。现象学方法以米氏方程的形式表达过氧化物酶的乒乓机制,并依据动力学参数[公式:见原文]、[公式:见原文]、kcat、[公式:见原文]、[公式:见原文]以及过氧化物酶共享的三步催化循环的微观速率常数k1和k3对这些效应进行解释。

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