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在十钒酸盐依赖的NADH氧化过程中氧气摄取爆发的一种新现象。

A novel phenomenon of burst of oxygen uptake during decavanadate-dependent oxidation of NADH.

作者信息

Kalyani P, Ramasarma T

机构信息

Department of Biochemistry, Indian Institute of Science, Bangalore.

出版信息

Mol Cell Biochem. 1993 Apr 7;121(1):21-9. doi: 10.1007/BF00928696.

Abstract

Oxidation of NADH by decavanadate, a polymeric form vanadate with a cage-like structure, in presence of rat liver microsomes followed a biphasic pattern. An initial slow phase involved a small rate of oxygen uptake and reduction of 3 of the 10 vanadium atoms. This was followed by a second rapid phase in which the rates of NADH oxidation and oxygen uptake increased several-fold with a stoichiometry of NADH: O2 of 1:1. The burst of NADH oxidation and oxygen uptake which occurs in phosphate, but not in Tris buffer, was prevented by SOD, catalase, histidine, EDTA, MnCl2 and CuSO4, but not by the hydroxyl radical quenchers, ethanol, methanol, formate and mannitol. The burst reaction is of a novel type that requires the polymeric structure of decavanadate for reduction of vanadium which, in presence of traces of H2O2, provides a reactive intermediate that promotes transfer of electrons from NADH to oxygen.

摘要

在大鼠肝微粒体存在的情况下,十钒酸盐(一种具有笼状结构的聚合钒酸盐)对NADH的氧化呈现双相模式。最初的缓慢阶段涉及少量的氧气摄取以及10个钒原子中的3个被还原。随后是第二个快速阶段,在此阶段中NADH氧化和氧气摄取的速率增加了几倍,NADH与O₂的化学计量比为1:1。在磷酸盐中而非Tris缓冲液中发生的NADH氧化和氧气摄取的爆发,可被超氧化物歧化酶(SOD)、过氧化氢酶、组氨酸、乙二胺四乙酸(EDTA)、氯化锰(MnCl₂)和硫酸铜(CuSO₄)抑制,但不能被羟基自由基淬灭剂乙醇、甲醇、甲酸盐和甘露醇抑制。这种爆发反应是一种新型反应,它需要十钒酸盐的聚合结构来还原钒,在存在微量过氧化氢(H₂O₂)的情况下,钒会提供一种反应性中间体,促进电子从NADH转移到氧气。

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