Stayton M M, Fromm H J
J Biol Chem. 1979 May 25;254(10):3765-71.
The enzyme D-ribulokinase from Aerobacter aerogenes was purified to near homogeneity. The molecular weight, as determined by Sephacryl gel chromatography, is 116,000. The subunit molecular weight, determined by sodium dodecyl sulfate-gel electrophoresis, is 59,000, suggesting that D-ribulokinase is a dimer of identical subunits. Initial rate kinetic studies, involving substrate analogs and products, were carried out. These investigations support a kinetic mechanism of the Random Bi Bi type. Isotope partitioning, utilizing D-[3H]ribulose, indicates that the mechanism is steady state Random Bi Bi.
产气气杆菌的D-核糖激酶被纯化至接近均一状态。通过Sephacryl凝胶色谱法测定,其分子量为116,000。通过十二烷基硫酸钠-凝胶电泳测定的亚基分子量为59,000,这表明D-核糖激酶是由相同亚基组成的二聚体。进行了涉及底物类似物和产物的初始速率动力学研究。这些研究支持随机双双型的动力学机制。利用D-[3H]核糖进行的同位素分配表明该机制为稳态随机双双机制。