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[大鼠肝细胞高尔基体中UDP-葡萄糖生物合成途径的存在]

[Presence of a pathway for biosynthesis of UDP-glucose in the Golgi apparatus of rat hepatocytes].

作者信息

Berthillier G, Got R

出版信息

Biochimie. 1977;59(1):85-9. doi: 10.1016/s0300-9084(77)80090-4.

Abstract

Glucokinase, phosphoglucomutase and glucose-1-phosphate uridylyltransferase are the three enzymes involved in a microsomic pathway for the synthesis of UDP glucose. Evidence is given, in this paper, for the localization of these three enzymes in a Golgi-rich fraction of rat liver. This fraction is prepared, from smooth microsomes, by the means of a discontinuous four-step sucrose gradient. Three of the lighter fractions (d = 1.08-1.13) are enriched in the Golgi markers (galactosyltransferase, sialytransferase and thiamin pyrophosphatase), especially the one with density 1.13. The three enzymes we are interested in are enriched in the two upper hands (d 1.08-1.11), which display an activity for the biosynthesis of UDP-glucose from glucose equivalent to the one obtained in a crude microsomic preparation, and which are not contaminated by other subcellular components.

摘要

葡萄糖激酶、磷酸葡萄糖变位酶和葡萄糖-1-磷酸尿苷酰转移酶是参与UDP葡萄糖合成的微粒体途径的三种酶。本文给出了这三种酶定位于大鼠肝脏富含高尔基体部分的证据。该部分是通过不连续的四步蔗糖梯度从光滑微粒体制备而来的。三个较轻的部分(密度d = 1.08 - 1.13)富含高尔基体标记物(半乳糖基转移酶、唾液酸转移酶和硫胺素焦磷酸酶),尤其是密度为1.13的部分。我们感兴趣的这三种酶在两个上层部分(密度d 1.08 - 1.11)中富集,这两个部分从葡萄糖合成UDP-葡萄糖的生物合成活性与粗微粒体制备物中获得的活性相当,并且未被其他亚细胞成分污染。

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