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使用反相高效液相色谱法测定肽基甘氨酸α-酰胺化单加氧酶将N-酰基甘氨酸转化为初级脂肪酸酰胺的过程。

Use of reversed phase HP liquid chromatography to assay conversion of N-acylglycines to primary fatty acid amides by peptidylglycine-alpha-amidating monooxygenase.

作者信息

Carpenter Tara, Poore Derek D, Gee Andrew J, Deshpande Pallavi, Merkler David J, Johnson Mitchell E

机构信息

Department of Chemistry and Biochemistry, Duquesne University, 308 Mellon Hall of Science, Pittsburgh, PA 15282-1530, USA.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Sep 25;809(1):15-21. doi: 10.1016/j.jchromb.2004.05.028.

Abstract

Primary fatty acid amides (R-CO-NH2) and N-acylglycines (R-CO-NH-CH2-COOH) are classes of compounds that have only recently been isolated and characterized from biological sources. Key questions remain regarding how these lipid amides are produced and degraded in biological systems. Relative to the fatty acids, little has been done to develop methods to separate and quantify the fatty acid amides and N-acylglycines. We describe reversed phase HPLC methods for the separation of C2-C12 primary fatty acid amides and N-acylglycines and also C12-C22 fatty acid amides. Separation within each class occurs primarily on the basis of simple interactions between the acyl chain and the chromatographic stationary phase, but the polar headgroups on these and related fatty acids and N-acylethanolamides modulate the absolute retention in reversed phase mode. We use these methods to measure the enzyme-mediated, two-step conversion of N-octanoylglycine to octanoamide.

摘要

伯脂肪酸酰胺(R-CO-NH2)和N-酰基甘氨酸(R-CO-NH-CH2-COOH)是最近才从生物源中分离和鉴定出来的两类化合物。关于这些脂质酰胺在生物系统中如何产生和降解,关键问题仍然存在。相对于脂肪酸,在开发分离和定量脂肪酸酰胺及N-酰基甘氨酸的方法方面进展甚微。我们描述了用于分离C2-C12伯脂肪酸酰胺和N-酰基甘氨酸以及C12-C22脂肪酸酰胺的反相高效液相色谱方法。每一类中的分离主要基于酰基链与色谱固定相之间的简单相互作用,但这些及相关脂肪酸和N-酰基乙醇胺上的极性头基会调节反相模式下的绝对保留时间。我们使用这些方法来测定酶介导的N-辛酰甘氨酸两步转化为辛酰胺的过程。

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