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[猫肝细胞低密度高尔基体组分中催化UDP-葡萄糖生物合成的酶的存在情况]

[Presence of enzymes catalyzing UDP-glucose biosynthesis in a low density Golgi fractions of cat hepatocytes].

作者信息

Azzar G, Berthillier G, Got R

出版信息

Biochimie. 1978;60(11-12):1339-42.

PMID:223665
Abstract

A Golgi-rich fraction is prepared from cat hepatocytes by the means of a four-step sucrose density gradient. The material applied to this gradient is composed either of smooth microsomes prepared from healthy animals, or of total microsomes prepared from cat treated by 50 per cent ethanol (0.6 g/100 g body weight, administered by stomach tube). A light fraction (d : 1.10) is obtained by the two procedures. It does not show any glucose-6-phosphatase activity, but is enriched in sialyltransferase, known as a marker enzyme for Golgi apparatus. It also contains the three enzymes implicated in the biosynthetic pathway for UDP-glucose (glucokinase, phosphoglucomutase and UTP : glucose-1-phosphate uridylyltransferase). UDP-glucose being the ultimate substrate in membranous glucosylation reactions, these results could support the hypothesis that sugar-nucleotides necessary for the glycoprotein biosynthesis are produced in the Golgi vesicles directly.

摘要

通过四步蔗糖密度梯度法从猫肝细胞中制备富含高尔基体的组分。应用于该梯度的材料要么由从健康动物制备的光滑微粒体组成,要么由经50%乙醇(0.6克/100克体重,通过胃管给药)处理的猫制备的总微粒体组成。通过这两种方法都可获得一个轻组分(密度:1.10)。它没有显示出任何葡萄糖-6-磷酸酶活性,但富含唾液酸转移酶,唾液酸转移酶是高尔基体的一种标志酶。它还含有参与UDP-葡萄糖生物合成途径的三种酶(葡萄糖激酶、磷酸葡萄糖变位酶和UTP:葡萄糖-1-磷酸尿苷酰转移酶)。UDP-葡萄糖是膜糖基化反应的最终底物,这些结果可能支持这样一种假说,即糖蛋白生物合成所需的糖核苷酸是在高尔基体囊泡中直接产生的。

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