Knogge W, Weissenböck G, Strack D
Z Naturforsch C Biosci. 1981 Mar-Apr;36(3-4):197-9. doi: 10.1515/znc-1981-3-402.
This report describes the separation of components from a 4-coumarate:CoA ligase assay by means of liquid chromatography. With the aid of polyamide column chromatography it is possible to enrich and isolate chromatographically and UV spectroscopically pure p-coumaroyl-CoA using as a solvent 0.01% NH4OH in methanol subsequent to water and methanol alone. High performance liquid chromatography on octadecylsilane-bonded silica stationary phase allows a discontinuous determination of ligase activity. All components - ATP, Coenzyme A, p-coumaric acid, and the products AMP and p-coumaroyl-CoA - can be separated and accurately quantified within 20 min using a water-acetonitrile gradient, containing 1% phosphoric acid. The presented HPLC method may be used to affirm the accuracy of optical tests.
本报告描述了通过液相色谱法从4-香豆酸:辅酶A连接酶测定中分离各组分的方法。借助聚酰胺柱色谱法,在仅用水和甲醇之后,使用0.01%氢氧化铵的甲醇溶液作为溶剂,可以通过色谱法和紫外光谱法富集并分离出色谱纯和光谱纯的对香豆酰辅酶A。在十八烷基硅烷键合硅胶固定相上进行的高效液相色谱法可实现连接酶活性的间断测定。使用含有1%磷酸的水-乙腈梯度,所有组分——三磷酸腺苷(ATP)、辅酶A、对香豆酸以及产物单磷酸腺苷(AMP)和对香豆酰辅酶A——均可在20分钟内分离并准确定量。所提出的高效液相色谱法可用于确认光学测试的准确性。