Whitman W B, Martin M N, Tabita F R
J Biol Chem. 1979 Oct 25;254(20):10184-9.
Ribulose 1,5-bisphosphate carboxylase from Rhodospirillum rubrum requires CO2 and Mg2+ for activation of both CO2, both the carboxylase and oxygenase activities are stimulated by 6-phoshpo-D-gluconate, fructose 1,6-bisphosphate, 2-phosphoglycolate, 3-phosphoglycerate, NADPH, and fructose 6-phosphate. The carboxylase activity is not activated by ribose 5-phosphate. The substrate, ribulose bisphosphate, neither activates nor inhibits the CO2 and Mg2+ activation of this enzyme. Activation by CO2 and Mg2+ is rapid and results in increased susceptibility to active-site-directed protein modification reagents. Because the R. rubrum carboxylase-oxygenase is a dimer of large subunits and contains no small subunits, these results suggest that the effector binding sites of the higher plant enzyme may also be found on the large subunit.
来自红螺菌的1,5-二磷酸核酮糖羧化酶需要二氧化碳和镁离子来激活羧化酶和加氧酶的活性,二者的活性均受到6-磷酸-D-葡萄糖酸、1,6-二磷酸果糖、2-磷酸乙醇酸、3-磷酸甘油酸、还原型辅酶Ⅱ和6-磷酸果糖的刺激。羧化酶活性不受5-磷酸核糖的激活。底物二磷酸核酮糖既不激活也不抑制该酶的二氧化碳和镁离子激活作用。二氧化碳和镁离子的激活作用迅速,且会导致对活性位点导向的蛋白质修饰试剂的敏感性增加。由于红螺菌羧化酶-加氧酶是大亚基的二聚体,不含小亚基,这些结果表明高等植物酶的效应物结合位点也可能存在于大亚基上。