NEW SPECTROPHOTOMETRIC ASSAY FOR ENZYMES OF PURINE METABOLISM .2. DETERMINATION OF GUANASE ACTIVITY

被引：9

作者：

HEINZ, F ^{[1
]}

RECKEL, S ^{[1
]}

KALDEN, JR ^{[1
]}

机构：

[1] UNIV ERLANGEN NURNBERG,INST & POLIKLIN KLIN IMMUNOL,D-8520 ERLANGEN,FED REP GER

来源：

ENZYME | 1979年 / 24卷 / 04期

关键词：

D O I：

10.1159/000458666

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

A new method for the determination of guanase is described. Xanthine, the product of the guanase reaction, is oxidized by xanthine oxidase, forming uric acid and hydrogen peroxide. Hydrogen peroxide is further reduced to water by catalase in the presence of ethanol. The acetaldehyde formed in this reaction step is dehydrogenated NAD or NADP dependent by aldehyde dehydrogenase. The NADH or NADPH production is measured and utilized for the calculation of the guanase activity. The sensitivity of the method can be doubled by the addition of uricase, which oxidizes uric acid to permit the formation of another mole of hydrogen peroxide.

引用

页码：247 / 254

页数：8

共 46 条

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