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开放系统中的振荡过氧化物酶-氧化酶反应。反应机理分析。

The oscillating peroxidase-oxidase reaction in an open system. Analysis of the reaction mechanism.

作者信息

Olsen L F

出版信息

Biochim Biophys Acta. 1978 Nov 10;527(1):212-20. doi: 10.1016/0005-2744(78)90270-x.

Abstract
  1. The oscillations in the peroxidase-oxidase reaction in an open system with NADH as the hydrogen donor are caused by the reaction starting and stopping at critical concentrations of the substrates O2 and NADH. The existence of such critical concentrations is typical of branched chain reactions. 2. The critical concentrations of O2 and NADH that determine the initiation of the reaction are mutually dependent. 3. The branching reactions that determine these critical concentrations involve compounds I and II. 4. Superoxide may be involved in the branching reactions by reacting with NADH and ferriperoxidase. At pH 5.1 the rate constant for the latter reaction is determined as 1.5 . 10(5) M-1 . s-1, whereas for the former reaction only an upper limit for the rate constant of 3.5 . 10(4) M-1 . s-1 could be estimated. These relatively low rate constants suggest that alternative branching reactions may also be involved.
摘要
  1. 以NADH作为氢供体的开放系统中,过氧化物酶-氧化酶反应的振荡是由反应在底物O₂和NADH的临界浓度下开始和停止所引起的。这种临界浓度的存在是支链反应的典型特征。2. 决定反应起始的O₂和NADH的临界浓度相互依赖。3. 决定这些临界浓度的分支反应涉及化合物I和II。4. 超氧化物可能通过与NADH和高铁过氧化物酶反应而参与分支反应。在pH 5.1时,后一反应的速率常数确定为1.5×10⁵ M⁻¹·s⁻¹,而对于前一反应,速率常数的上限仅估计为3.5×10⁴ M⁻¹·s⁻¹。这些相对较低的速率常数表明也可能涉及其他分支反应。

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