Hauser M J, Olsen L F
Physical Biochemistry Group, Odense University, Forskerparken 10, DK-5230 Odense M, Denmark.
Biochemistry. 1998 Feb 24;37(8):2458-69. doi: 10.1021/bi972424k.
The influence of a series of naturally occurring phenolic compounds on the dynamics of the horseradish peroxidase-catalyzed oxidation of NADH by oxygen (the peroxidase-oxidase reaction) was investigated. Various types of dynamic behaviors are induced in the peroxidase-oxidase reaction upon addition of low concentrations of different phenols. The identity of the particular phenol determines the type of dynamics shown (inhibition of the reaction, monotonic reaction, damped oscillations, sustained oscillations, and complex oscillations). The kind of behavior that a given phenolic compound is able to induce is governed by the reduction potentials for the formation of the phenoxyl radical. The phenolic compounds are shown not to be consumed during the reaction. Mechanistic considerations are made on the basis of the reduction potentials of the different reactants present in the peroxidase-oxidase system. We interpret the role of the phenols as electron mediators of the electron transfer between some enzyme intermediates or O2- and NADH.
研究了一系列天然存在的酚类化合物对辣根过氧化物酶催化氧气氧化NADH的动力学(过氧化物酶-氧化酶反应)的影响。在过氧化物酶-氧化酶反应中加入低浓度的不同酚类会诱导出各种类型的动力学行为。特定酚类的特性决定了所呈现的动力学类型(反应抑制、单调反应、阻尼振荡、持续振荡和复杂振荡)。给定酚类化合物能够诱导的行为类型由苯氧自由基形成的还原电位决定。结果表明,酚类化合物在反应过程中不会被消耗。基于过氧化物酶-氧化酶系统中存在的不同反应物的还原电位进行了机理探讨。我们将酚类的作用解释为一些酶中间体或O2-与NADH之间电子转移的电子介质。