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两相体系中磷脂酶C的活性

Activity of phospholipase C in two-phase systems.

作者信息

Haftendorn Regine, Ulbrich-Hofmann Renate

机构信息

Department of Biochemistry/Biotechnology, Martin-Luther University Halle-Wittenberg, Halle, Germany.

出版信息

Anal Biochem. 2002 Jul 1;306(1):144-7. doi: 10.1006/abio.2002.5692.

Abstract

Although phospholipase C (PLC) is known to be activated by water-insoluble organic solvents, most activity assays have been designed to work in an aqueous milieu. Here a sensitive method is described for the determination of PLC activity in two-phase systems. The assay is based on the hydrolysis of phosphatidylcholine (PC) in chloroform/buffer. The initial rates of the reaction are determined by densitometric quantification of the product 1,2-diacylglycerol after its separation by high-performance TLC and staining with a CuSO4/H3PO4 or p-methoxybenzaldehyde/H2SO4 reagent. The method is examined for the determination of Vmax and Km values of PCs with varying length acyl chains (C10-C18). The comparison of the kinetic parameters with the Vmax and Km values of the same substrates in the conventional titrimetric assay, using sodium deoxycholate for micellization of PC, demonstrates the high efficiency of PLC in the two-phase emulsion system.

摘要

尽管已知磷脂酶C(PLC)可被水不溶性有机溶剂激活,但大多数活性测定方法都是设计用于在水性环境中进行的。本文描述了一种用于测定两相系统中PLC活性的灵敏方法。该测定基于氯仿/缓冲液中磷脂酰胆碱(PC)的水解。通过高效薄层层析分离产物1,2-二酰基甘油并用硫酸铜/磷酸或对甲氧基苯甲醛/硫酸试剂染色后,通过光密度定量法测定反应的初始速率。该方法用于测定具有不同长度酰基链(C10 - C18)的PC的Vmax和Km值。将动力学参数与传统滴定法中相同底物的Vmax和Km值进行比较,传统滴定法使用脱氧胆酸钠使PC形成胶束,结果表明PLC在两相乳液系统中具有高效性。

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