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芳香化酶及相关碳-碳键裂解细胞色素P450酶的机制研究。

Mechanistic studies on aromatase and related C-C bond cleaving P-450 enzymes.

作者信息

Akhtar M, Njar V C, Wright J N

机构信息

Department of Biochemistry, University of Southampton, Highfield, England.

出版信息

J Steroid Biochem Mol Biol. 1993 Mar;44(4-6):375-87. doi: 10.1016/0960-0760(93)90241-n.

Abstract

Some P-450 systems, notably aromatase and 14 alpha-demethylase catalyse not only the hydroxylate reaction but also the oxidation of an alcohol into a carbonyl compound as well as a C-C bond cleavage process. All these reactions occur at the same active site. A somewhat analogous situation is noted with 17 alpha-hydroxylase-17,20-lyase that participates in hydroxylation as well as C-C bond cleavage process. The C-C bond cleavage reactions catalysed by the above enzymes conform to the general equation: [formula: see text] It is argued that all three types of reaction catalyzed by these enzymes may be viewed as variations on a common theme. In P-450 dependent hydroxylation the initially formed FeIII-O-O. species is converted into FeIII-O-OH and the heterolysis of the oxygen-oxygen bond of the latter then gives the oxo-derivative for which a number of canonical structures are possible; for example FeV = O<==>(+.)FeIV = O<==>FeIV-O.. One of these, FeIV-O. behaves like an alkoxyl radical and participates in hydrogen abstraction from C-H bond to produce FeIV-OH and carbon radical. The latter is then quenched by the delivery of hydroxyl radical from FeIV-OH. The latter species may thus be regarded as a carrier of hydroxyl radical. We have proposed that the C-C bond cleavage reaction occurs through the participation of the FeIII-O-OH species that is trapped by the electrophilic property of the carbonyl compound giving a peroxide adduct that fragments to produce an acyl-carbon cleavage. Scientific developments leading up to this conclusion are considered. In the first author's views, "The study of mechanisms is not a scientific but a cultural activity. Mechanisms do not aim at an absolute truth but are intended to be a "running" commentary on the status of knowledge in a field. As the structural knowledge in a field advances Mechanisms evolve to take note of the new findings. Just as a constructive "running" commentary provides the stimulus for higher standards of performance, so Mechanisms call for better and firmer structural information from their practitioners".

摘要

一些细胞色素P-450系统,特别是芳香化酶和14α-脱甲基酶,不仅催化羟基化反应,还催化醇氧化为羰基化合物以及碳-碳键裂解过程。所有这些反应都发生在同一个活性位点。17α-羟化酶-17,20-裂解酶也存在类似情况,它参与羟基化以及碳-碳键裂解过程。上述酶催化的碳-碳键裂解反应符合以下通式:[公式:见原文]。有人认为,这些酶催化的所有三种类型的反应都可视为同一主题的变体。在细胞色素P-450依赖性羟基化反应中,最初形成的FeIII-O-O.物种会转化为FeIII-O-OH,后者氧-氧键的异裂会产生多种可能的氧代衍生物的经典结构;例如FeV = O<==>(+.)FeIV = O<==>FeIV-O.. 其中之一,FeIV-O.的行为类似于烷氧基自由基,参与从C-H键夺取氢以生成FeIV-OH和碳自由基。后者随后被FeIV-OH提供的羟基自由基淬灭。因此,后者物种可被视为羟基自由基的载体。我们提出,碳-碳键裂解反应是通过FeIII-O-OH物种的参与而发生的,该物种被羰基化合物的亲电性质捕获,形成过氧化物加合物,然后裂解产生酰基-碳裂解。本文考虑了得出这一结论的科学发展过程。第一作者认为,“机制研究并非一项科学活动,而是一种文化活动。机制并非旨在追求绝对真理,而是旨在对一个领域的知识现状进行‘动态’评论。随着一个领域的结构知识不断进步,机制也会不断演变以关注新发现。正如建设性的‘动态’评论能激发更高的表现标准一样,机制也要求其实践者提供更好、更可靠的结构信息”。

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