Mack D O, Suen E T, Girardot J M, Miller J A, Delaney R, Johnson B C
J Biol Chem. 1976 Jun 10;251(11):3269-76.
The vitamin K-dependent carboxylating system has been solubilized by Lubrol PX or Triton X-100 treatment of vitamin K-deficient rat liver microsomes. As obtained from vitamin K-deficient rat liver, this soluble preparation is dependent upon the in vitro addition of vitamin K1 for carboxylating activity. The enzyme system is complex and is dependent upon NADH and dithiothreitol for maximum activity. While detergents used to solubilize the enzyme complex do markedly inhibit the activity of the system, the solubilized system is still highly responsive to vitamin K addition and can be used for further study of the carboxylating enzyme system. The requirement for dithiothreitol and the inhibition by p-hydroxymercuribenzoate indicate the involvement of an --SH enzyme in the carboxylating system.
通过用Lubrol PX或Triton X - 100处理维生素K缺乏的大鼠肝微粒体,维生素K依赖的羧化系统已被溶解。从维生素K缺乏的大鼠肝脏中获得的这种可溶性制剂,其羧化活性依赖于体外添加维生素K1。该酶系统很复杂,最大活性依赖于NADH和二硫苏糖醇。虽然用于溶解酶复合物的去污剂确实会显著抑制该系统的活性,但溶解后的系统对添加维生素K仍有高度反应,可用于羧化酶系统的进一步研究。对二硫苏糖醇的需求以及对对羟基汞苯甲酸的抑制表明在羧化系统中有一种含巯基的酶参与。