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假氨基糖对大鼠肝脏寡糖葡糖苷酶I和II以及溶酶体α-葡糖苷酶的抑制作用。

Inhibitory effect of pseudo-aminosugars on oligosaccharide glucosidases I and II and on lysosomal alpha-glucosidase from rat liver.

作者信息

Takeuchi M, Kamata K, Yoshida M, Kameda Y, Matsui K

机构信息

Department of Biochemistry, School of Pharmacy, Hokuriku University, Ishikawa.

出版信息

J Biochem. 1990 Jul;108(1):42-6. doi: 10.1093/oxfordjournals.jbchem.a123160.

Abstract

We examined the inhibitory effect of three pseudo-aminosugars (validamine, valienamine, and valiolamine), which were isolated from the broth of Streptomyces hygroscopicus, on the oligosaccharide-processing glucosidases I and II involved in glycoprotein biosynthesis in rat liver. Both glucosidases I and II were inhibited to the same extent by the pseudoaminosugars, and valiolamine had a more potent inhibitory activity than validamine or valienamine. A 50% inhibition of valiolamine was observed at 12 microM for glucosidase I and glucosidase II activities acting respectively on the substrates Glc3Man9GlcNAc2 and p-nitrophenyl alpha-D-glucopyranoside. Further, in order to investigate further the ability of valiolamine to inhibit glucosidase I, reaction products were analyzed by gel filtration on a Bio-Gel P-4 column. We also compared the inhibitory action of these pseudo-aminosugars on the acid alpha-glucosidase of rat liver lysosomes. They competitively inhibited the hydrolysis of both substrates, maltose and glycogen. Valiolamine again had a more potent lysosomal alpha-glucosidase inhibitory activity than the other two. The Ki values of valiolamine for the hydrolysis of maltose and glycogen were 8.1 and 11 microM, respectively. Valiolamine is a particularly effective inhibitor of oligosaccharide glucosidases I and II and of lysosomal alpha-glucosidase. Hence valiolamine might be useful as a research tool in investigations of carbohydrate metabolism.

摘要

我们研究了从吸水链霉菌发酵液中分离得到的三种假氨基糖(有效胺、井冈胺和伏格列波糖)对大鼠肝脏中参与糖蛋白生物合成的寡糖加工葡糖苷酶I和II的抑制作用。假氨基糖对葡糖苷酶I和II的抑制程度相同,伏格列波糖的抑制活性比有效胺或井冈胺更强。对于分别作用于底物Glc3Man9GlcNAc2和对硝基苯基α-D-吡喃葡萄糖苷的葡糖苷酶I和葡糖苷酶II活性,在12 microM时观察到伏格列波糖有50%的抑制率。此外,为了进一步研究伏格列波糖抑制葡糖苷酶I的能力,通过在Bio-Gel P-4柱上进行凝胶过滤分析反应产物。我们还比较了这些假氨基糖对大鼠肝脏溶酶体酸性α-葡糖苷酶的抑制作用。它们竞争性抑制麦芽糖和糖原这两种底物的水解。伏格列波糖对溶酶体α-葡糖苷酶的抑制活性再次比其他两种更强。伏格列波糖水解麦芽糖和糖原的Ki值分别为8.1和11 microM。伏格列波糖是寡糖葡糖苷酶I和II以及溶酶体α-葡糖苷酶的一种特别有效的抑制剂。因此,伏格列波糖可能作为研究碳水化合物代谢的一种研究工具而有用。

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