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以甘氨酰脯氨酸对苯偶氮苯胺为底物的人血清中X-脯氨酰二肽基氨基肽酶活性的新检测方法。

A new assay of X-prolyl dipeptidyl-aminopeptidase activity in human serum with glycylproline p-phenylazoanilide as substrate.

作者信息

Kato T, Iwase K, Nagatsu T, Hino M, Takemoto T, Sakakibara S

出版信息

Mol Cell Biochem. 1979 Mar 5;24(1):9-13. doi: 10.1007/BF00220189.

Abstract

A new assay procedure for X-prolyl dipeptidyl-aminopeptidase activity in human serum was developed with glycylproline p-phenylazoanilide tosylate as substrate. p-Phenylazoaniline liberated by the enzyme reaction was measured photometrically at 493 nm after stopping the reaction with acid. This assay was simple and sensitive, and less than 50 microliter of human serum was required for the assay. Km value was 2.5 mM and the optimum pH was 8.7. After disc gel electrophoresis of human serum, the enzyme activity could be distinctly observed as a reddish band on the gel when the gel was incubated with this substrate.

摘要

以甲苯磺酸甘氨酰脯氨酸对苯偶氮苯胺为底物,建立了一种新的人血清X-脯氨酰二肽基氨基肽酶活性检测方法。酶反应释放出的对苯偶氮苯胺在用酸终止反应后,于493nm处进行光度测定。该检测方法简单且灵敏,检测所需人血清量少于50微升。米氏常数为2.5mM,最适pH为8.7。对人血清进行圆盘凝胶电泳后,当凝胶与该底物一起孵育时,可在凝胶上清晰地观察到酶活性呈现为一条红色条带。

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