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大鼠肾皮质微粒体中的脂肪酸羟基化作用

Fatty acid hydroxylation in rat kidney cortex microsomes.

作者信息

Ellin A, Orrenius S

出版信息

Mol Cell Biochem. 1975 Aug 30;8(2):69-79. doi: 10.1007/BF02116235.

Abstract

Rat kidney microsomes have been found to catalyze the hydroxylation of medium-chained fatty acids to the omega- and (omego-1)-hydroxy derivatives. This reaction, which requires NADPH and molecular oxygen, is a function of monooxygenase system present in the kidney microsomes, containing NADPH-cytochrome c reductase and cytochrome P-450K. NADH is about half as effective as an electron donor as NADPH and there is an additive effect in the presence of both nucleotides. Cytochrome P-450K absorbs light maximally at 452-3 nm, when it is reduced and bound to carbon monoxide. The extinction coefficient of this complex is 91 mM(-1) cm(-1). Electrons from NADPH are transferred to cytochrome P-450K via the NADPH-cytochrome c reductase. The reduction rate of cytochrome P-450K is stimulated by added fatty acids and the reduction kinetics reveal the presence of endogenous substrates bound to cytochrome P-450K. Both cytochrome P-450K concentration and fatty acid hydroxylation activity in kidney microsomes are increased by starvation. On the other hand, phenobarbital treatment of the rats has no effect on either the hemoprotein or the overall hydroxylation reaction and 3,4-benzpyrene administration induces a new species of cytochrome P-450K not involved in fatty acid hydroxylation. Cytochrome P-450K shows, in contrast to liver P-450, high substrate specificity. The only substances forming enzyme-substrate complexes with cytochrome P-450K are the medium-chained fatty acids and certain derivatives of these acids. The chemical requirements for substrate binding include a carbon chain of medium length and at the end of the chain a carbonyl group and a free electron pair on a neighbouring atom. The distance between the binding site for the carbonyl group and the active oxygen is suggested to be in the order of 16 A. This distance fixes the ratio of omega- and (omega-1)-hydroxylated products formed from a certain fatty acid by the single species of cytochrome P-450K involved. The membrane microenvironment seems also to be of importance for the substrate specificity of cytochrome P-450K, since removal of the cytochrome from the membrane lowers its binding specificity to some extent. A comparison between the liver and kidney cytochrome P-450 systems suggests that the kidney cytochrome P-450K system is specialized for fatty acid hydroxylation.

摘要

已发现大鼠肾微粒体能催化中链脂肪酸羟基化为ω-和(ω-1)-羟基衍生物。该反应需要NADPH和分子氧,是肾微粒体中存在的单加氧酶系统的功能,该系统含有NADPH-细胞色素c还原酶和细胞色素P-450K。NADH作为电子供体的效率约为NADPH的一半,并且在两种核苷酸同时存在时具有累加效应。细胞色素P-450K在还原并与一氧化碳结合时,在452 - 3nm处有最大吸光值。该复合物的消光系数为91 mM⁻¹cm⁻¹。来自NADPH的电子通过NADPH-细胞色素c还原酶转移到细胞色素P-450K。添加脂肪酸可刺激细胞色素P-450K的还原速率,还原动力学揭示了与细胞色素P-450K结合的内源性底物的存在。饥饿会增加肾微粒体中细胞色素P-450K的浓度和脂肪酸羟基化活性。另一方面,用苯巴比妥处理大鼠对血红素蛋白或整体羟基化反应均无影响,而给予3,4-苯并芘会诱导出一种不参与脂肪酸羟基化的新型细胞色素P-450K。与肝脏P-450相比,细胞色素P-450K具有较高的底物特异性。唯一能与细胞色素P-450K形成酶-底物复合物的物质是中链脂肪酸及其某些衍生物。底物结合的化学要求包括中等长度的碳链,且在链的末端有一个羰基和相邻原子上的一对自由电子。羰基结合位点与活性氧之间的距离被认为约为16 Å。这个距离决定了由参与反应的单一细胞色素P-450K从某种脂肪酸形成的ω-和(ω-1)-羟基化产物的比例。膜微环境似乎对细胞色素P-450K的底物特异性也很重要,因为从膜上除去细胞色素会在一定程度上降低其结合特异性。肝脏和肾脏细胞色素P-450系统的比较表明,肾脏细胞色素P-450K系统专门用于脂肪酸羟基化。

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