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线粒体柠檬酸合酶在体内被固定化。

Mitochondrial citrate synthase is immobilized in vivo.

作者信息

Haggie P M, Brindle K M

机构信息

University of Cambridge, Department of Biochemistry, Old Addenbrooke's Site, 80 Tennis Court Road, Cambridge CB2 1GA, United Kingdom.

出版信息

J Biol Chem. 1999 Feb 12;274(7):3941-5. doi: 10.1074/jbc.274.7.3941.

Abstract

The enzymes of the tricarboxylic acid cycle in the mitochondrial matrix are proposed to form a multienzyme complex, in which there is channeling of substrates between enzyme active sites. However no direct evidence has been obtained in vivo for the involvement of these enzymes in such a complex. We have labeled the tricarboxylic acid cycle enzyme, citrate synthase 1, in the yeast Saccharomyces cerevisiae, by biosynthetic incorporation of 5-fluorotryptophan. Comparison of the 19F NMR resonance intensities from the labeled enzyme in the intact cell and in cell-free lysates indicated that the enzyme is motionally restricted in vivo, consistent with its participation in a multienzyme complex.

摘要

线粒体基质中的三羧酸循环酶被认为形成了一种多酶复合体,其中底物在酶活性位点之间进行通道运输。然而,尚未在体内获得这些酶参与这种复合体的直接证据。我们通过生物合成掺入5-氟色氨酸,对酿酒酵母中的三羧酸循环酶柠檬酸合酶1进行了标记。对完整细胞和无细胞裂解物中标记酶的19F NMR共振强度进行比较,结果表明该酶在体内的运动受到限制,这与其参与多酶复合体的情况相符。

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