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维生素K依赖性羧化酶:不同体系中外源底物的羧化作用

Vitamin K-dependent carboxylase: the carboxylation of exogenous substrates in different systems.

作者信息

de Boer-van den Berg M A, Ulrich M M, Hemker H C, Soute B A, Vermeer C

出版信息

Biochim Biophys Acta. 1985 Sep 20;831(1):94-8. doi: 10.1016/0167-4838(85)90154-2.

Abstract

Two types of solid-phase carboxylase, SPC-II and SPC-X, have been prepared from the livers of warfarin-treated cows. Their enzymatic activities were compared with substrate-free carboxylase in microsomes from normal cows and substrate-bound carboxylase in microsomes from warfarin-treated cows. A number of exogenous substrates for carboxylase have been purified and tested. We found that large substrates, such as descarboxyprothrombin, are carboxylated only by substrate-free carboxylase and not by the substrate-bound enzyme. No differences in apparent Km values between solid-phase carboxylases II and X were observed.

摘要

已从接受华法林治疗的奶牛肝脏中制备出两种固相羧化酶,即SPC-II和SPC-X。将它们的酶活性与正常奶牛微粒体中的无底物羧化酶以及接受华法林治疗的奶牛微粒体中的底物结合羧化酶进行了比较。已纯化并测试了多种羧化酶的外源底物。我们发现,大的底物,如脱羧凝血酶原,仅被无底物羧化酶羧化,而不被底物结合酶羧化。未观察到固相羧化酶II和X之间表观Km值的差异。

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