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一种用于测定磷脂代谢中胞苷5'-二磷酸-1,2-二酰基-sn-甘油依赖性酶的分光光度法。

A spectrophotometric method for the assay of cytidine 5'-diphospho-1,2-diacyl-sn-glycerol-dependent enzymes of phospholipid metabolism.

作者信息

Carman G M, Dowhan W

出版信息

J Lipid Res. 1978 May;19(4):519-22.

PMID:207804
Abstract

Cytidine 5'-diphospho-1,2-diacyl-sn-glycerol (CDP-diglyceride) hydrolase, CDP-diglyceride:L-serine O-phosphatidyltransferase, and CDP-diglyceride:sn-glycero-3-phosphate phosphatidyltransferase all release CMP from their liponucleotide substrate, CDP-diglyceride. We have developed a spectrophotometric assay for these enzymes using CMP kinase, pyruvate kinase, and lactate dehydrogenase to couple the release of CMP with the oxidation of NADH. The assay for each of the phospholipid-dependent enzymes was found to be linear both with time and with enzyme concentration. The assay should prove useful for continuous monitoring of enzymatic activity, determination of initial rates of reaction, and detailed kinetic analysis of these enzymes. Since several enzymes and substrates are used in the coupled assay system, the method is limited to analysis of partially purified preparations lacking competing activities.

摘要

胞苷5'-二磷酸-1,2-二酰基-sn-甘油(CDP-二甘油酯)水解酶、CDP-二甘油酯:L-丝氨酸O-磷脂酰转移酶和CDP-二甘油酯:sn-甘油-3-磷酸磷脂酰转移酶均从其脂核苷酸底物CDP-二甘油酯中释放出CMP。我们利用CMP激酶、丙酮酸激酶和乳酸脱氢酶开发了一种分光光度法来检测这些酶,以便将CMP的释放与NADH的氧化偶联起来。发现每种磷脂依赖性酶的检测方法在时间和酶浓度方面均呈线性关系。该检测方法对于连续监测酶活性、测定反应初速率以及对这些酶进行详细的动力学分析应是有用的。由于在偶联检测系统中使用了几种酶和底物,该方法仅限于分析缺乏竞争活性的部分纯化制剂。

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