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新合成的DT-黄递酶在大鼠肝脏中的分布

Distribution of newly synthesized DT-diaphorase in rat liver.

作者信息

Edlund C, Elhammer A, Dallner G

出版信息

Biosci Rep. 1982 Nov;2(11):861-5. doi: 10.1007/BF01114891.

Abstract

The distribution, synthesis, transport, and glycosylation of rat-liver DT-diaphorase has been investigated. The enzyme could be isolated using specific antibodies, mainly from the soluble supernatant but also from microsomal vesicles, Golgi membranes, and mitochondria. 40% of the microsomal enzyme was located in the lumen or on the interior side of the membrane, the rest remaining as an integral non-extractable part of the membrane. Synthesis of DT-diaphorase takes place on both free and bound ribosomes, although it was found to be transported in a sequential manner from the rough to the smooth endoplasmic reticulum and also subsequently to the mitochondria. The rough and smooth microsomal DT-diaphorase contains covalently bound carbohydrate, but no sugar moiety could be detected bound to the cytoplasmic form of the enzyme.

摘要

对大鼠肝脏DT-黄递酶的分布、合成、运输和糖基化进行了研究。该酶可用特异性抗体分离,主要来自可溶性上清液,但也可从微粒体囊泡、高尔基体膜和线粒体中分离得到。40%的微粒体酶位于膜腔或膜内侧,其余则作为膜的不可提取的整合部分保留。DT-黄递酶在游离核糖体和结合核糖体上均有合成,尽管发现它以有序方式从糙面内质网运输到滑面内质网,随后也运输到线粒体。糙面和滑面微粒体DT-黄递酶含有共价结合的碳水化合物,但未检测到与该酶胞质形式结合的糖部分。

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