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[NADPH-细胞色素c还原酶产生氧阴离子自由基与人工受体及细胞色素P-450还原之间的相互关系]

[Interrelationship between the generation of oxygen anion-radicals and the reduction of artificial acceptors and cytochrome P-450 by NADPH-cytochrome c reductase].

作者信息

Liakhovich V V, Mishin V M, Pokrovskii A G

出版信息

Biokhimiia. 1977 Jul;42(7):1323-30.

PMID:198028
Abstract

The interaction of NADPH-cytochrome c reductase with oxygen, artificial acceptors and cytochrome P-450 is investigated. It is found that generation of oxygen anion-radicals (O2-), determined from the reaction of adrenaline oxidation into adrenochrome, proceeds independently on the reactions of interaction with artificial "anaerobic" acceptors-cytochrome c, dichlorophenolindophenol. Propylgallate competitively inhibits the reaction of adrenaline oxidation by isolated DADPH-cytochrome c reductase and non-competitively suppress the reaction of cytochrome c reduction. In contrast to the process of electron transfer on cytochrome c, there is a direct correlation between the rate of cytochrome P-450 reduction and the rate of adrenaline oxidation in liver microsomes. Hexobarbital increases V of the adrenaline oxidation reaction and does not affect the Km value, while metirapon, a metabolic inhibitor, decreases the Vmax and does not change Km. On the basis of the data obtained it is suggested that the reactions of NADPH-cytochrome c reductase interaction with oxygen and artificial "anaerobic" acceptors are connected with different redox-states of flavoprotein or with different flavine coenzymes, and that the electron transport on cytochrome P-450 and directly on oxygen takes place in interrelated redox-states of flavoprotein.

摘要

研究了NADPH-细胞色素c还原酶与氧、人工受体及细胞色素P-450的相互作用。发现由肾上腺素氧化生成肾上腺色素反应所测定的氧阴离子自由基(O2-)的生成,独立于与人工“厌氧”受体——细胞色素c、二氯酚靛酚的相互作用反应。棓丙酯竞争性抑制分离的DADPH-细胞色素c还原酶催化的肾上腺素氧化反应,并非竞争性抑制细胞色素c还原反应。与细胞色素c上的电子传递过程不同,肝微粒体中细胞色素P-450的还原速率与肾上腺素氧化速率之间存在直接相关性。己巴比妥增加肾上腺素氧化反应的V值,而不影响Km值,而代谢抑制剂美替拉酮则降低Vmax且不改变Km。根据所得数据表明,NADPH-细胞色素c还原酶与氧及人工“厌氧”受体的相互作用反应与黄素蛋白的不同氧化还原状态或不同的黄素辅酶有关,并且细胞色素P-450上以及直接在氧上的电子传递发生在黄素蛋白相互关联的氧化还原状态中。

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