Soute B A, de Metz M, Vermeer C
FEBS Lett. 1982 Sep 20;146(2):365-8. doi: 10.1016/0014-5793(82)80954-x.
Bovine liver vitamin K-dependent carboxylase was compared with that obtained from human liver and placenta. Human liver microsomal preparations contained more endogenous substrate than did bovine preparations, but no differences were found between the two types of hepatic enzyme. This observation demonstrates that the bovine liver carboxylating enzyme system is a good model system which will help us to understand vitamin K action in man. Placental carboxylase differed from the liver systems because only vitamin K hydroquinone and not vitamin K quinone could be used as a coenzyme for the carboxylation reaction. Obviously, vitamin K reductase was absent in these preparations.
将牛肝维生素K依赖性羧化酶与从人肝和胎盘中获得的该酶进行了比较。人肝微粒体制剂比牛肝制剂含有更多的内源性底物,但两种类型的肝酶之间未发现差异。这一观察结果表明,牛肝羧化酶系统是一个很好的模型系统,将有助于我们了解维生素K在人体内的作用。胎盘羧化酶与肝脏系统不同,因为只有维生素K对苯二酚而不是维生素K醌可作为羧化反应的辅酶。显然,这些制剂中不存在维生素K还原酶。