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乳液体系中磷脂酶D活性的测定

The determination of phospholipase D activity in emulsion systems.

作者信息

Aurich I, Hirche F, Ulbrich-Hofmann R

机构信息

Department of Biochemistry/Biotechnology, Martin-Luther University Halle-Wittenberg, Kurt-Mothes-Strasse 3, Halle, D-06120, Germany.

出版信息

Anal Biochem. 1999 Mar 15;268(2):337-42. doi: 10.1006/abio.1998.3072.

Abstract

Although phospholipase D (PLD) is often used in emulsion systems consisting of buffer and a nonpolar organic solvent, most activity assays have been designed to work in purely aqueous milieu. Here a method is described for the determination of PLD activity in emulsion systems. The assay is based on the transphosphatidylation of phosphatidylcholine with 1-butanol in dichloromethane/buffer with the subsequent densitometric quantification of the products after their separation by HPTLC and staining with a CuSO4/H3PO4 reagent. The method is particularly appropriate for the determination of enzymes such as PLD from Streptomyces sp. that prefer the exchange of the head group in glycerophospholipids to their hydrolysis. Since the application of an organic solvent in the PLD assay allows the determination of the enzyme in analytes insoluble in aqueous media, the method can also be used to determine PLD activity in the presence of high concentrations of phospholipids.

摘要

尽管磷脂酶D(PLD)常用于由缓冲液和非极性有机溶剂组成的乳液体系中,但大多数活性测定方法都是设计用于在纯水性环境中进行的。本文描述了一种用于测定乳液体系中PLD活性的方法。该测定基于磷脂酰胆碱在二氯甲烷/缓冲液中与1-丁醇的转磷脂酰基作用,随后通过HPTLC分离并用CuSO4/H3PO4试剂染色后对产物进行光密度定量。该方法特别适用于测定来自链霉菌属等的酶,如PLD,这类酶更倾向于甘油磷脂中头部基团的交换而非水解。由于在PLD测定中使用有机溶剂能够测定不溶于水性介质的分析物中的酶,该方法也可用于在高浓度磷脂存在的情况下测定PLD活性。

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