Wood G M, Suttie J W
Department of Biochemistry, College of Agricultural and Life Sciences, University of Wisconsin-Madison 53706.
J Biol Chem. 1988 Mar 5;263(7):3234-9.
The rat liver microsomal vitamin K-dependent carboxylase catalyzes the carboxylation of peptide-bound glutamyl residues to gamma-carboxyglutamyl (Gla) residues with the concomitant formation of vitamin K 2,3-epoxide (KO). These studies have demonstrated that the half-reaction, formation of KO, occurs in the absence of carboxylation at low glutamyl substrate concentration but that the ratio of KO/Gla approaches unity as the glutamyl substrate concentration is increased. Utilization of the carboxylase substrate Phe-Leu-[gamma-3H] Glu-Glu-Leu has demonstrated that the ratios of KO/gamma-C-H bonds cleaved and Gla/gamma-C-H bonds cleaved are equivalent at high substrate concentrations and that these ratios approach unity. At low substrate concentrations, KO formation occurs at a higher rate than gamma-H bond cleavage. These data are consistent with a mechanism involving the formation of an oxygenated intermediate from vitamin KH2 and O2 that is converted to KO during hydrogen abstraction from the gamma-position of the Glu substrate. In the absence of a Glu substrate, the intermediate is converted to KO by a mechanism not coupled to glutamyl activation.
大鼠肝脏微粒体维生素K依赖性羧化酶催化肽结合的谷氨酰残基羧化为γ-羧基谷氨酰(Gla)残基,并伴随维生素K 2,3-环氧化物(KO)的形成。这些研究表明,在低谷氨酰底物浓度下,半反应即KO的形成在没有羧化作用时发生,但随着谷氨酰底物浓度的增加,KO/Gla的比值接近1。使用羧化酶底物苯丙氨酸-亮氨酸-[γ-3H]谷氨酸-谷氨酸-亮氨酸已证明,在高底物浓度下,KO/γ-C-H键断裂的比值与Gla/γ-C-H键断裂的比值相等,且这些比值接近1。在低底物浓度下,KO的形成速率高于γ-H键的断裂速率。这些数据与一种机制相符,该机制涉及从维生素KH2和O2形成一种氧化中间体,该中间体在从Glu底物的γ位夺取氢的过程中转化为KO。在没有Glu底物的情况下,中间体通过一种不与谷氨酰激活偶联的机制转化为KO。