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猪脑醛糖还原酶的亲和纯化及性质

Affinity purification and properties of porcine brain aldose reductase.

作者信息

Boghosian R A, McGuinness E T

出版信息

Biochim Biophys Acta. 1979 Apr 12;567(2):278-86. doi: 10.1016/0005-2744(79)90113-x.

Abstract

Aldose reductase (alditol:NADP+ 1-oxidoreductase, EC 1.1.1.21) has been purified 1500-fold from porcine brain in a four-step procedure employing Blue-Sepharose 6B affinity chromatography. The purified enzyme was shown to be apparently homogeneous by polyacrylamide gel electrophoresis. The enzyme is a single chain polypeptide of molecular weight 40 000, pH optimum 5.0 K(app)(xylose) 4 mM; K(app)(NADPH) 3 microM. The relative substrate activities, activation with sulfate ion, and limited oxidative and NADH-related reductive activities confirm the classification of this enzyme as aldolase reductase. The activity of the reductase with p-nitrobenzaldehyde and 3-indolacetaldehyde and the similarity of its physical properties with the 'low Km' aldehyde reductase of porcine brain previously reported indicates that these enzymes may be identical.

摘要

醛糖还原酶(醛糖醇:NADP⁺ 1-氧化还原酶,EC 1.1.1.21)已通过采用Blue-Sepharose 6B亲和色谱的四步程序从猪脑中纯化了1500倍。通过聚丙烯酰胺凝胶电泳显示纯化的酶明显均一。该酶是一种分子量为40000的单链多肽,最适pH为5.0,K(app)(木糖)为4 mM;K(app)(NADPH)为3 μM。相对底物活性、硫酸根离子激活以及有限的氧化和NADH相关还原活性证实了该酶属于醛糖还原酶。该还原酶对对硝基苯甲醛和3-吲哚乙醛的活性及其物理性质与先前报道的猪脑“低Km”醛还原酶的相似性表明这些酶可能是相同的。

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