Etiemble J, Picat C, Boivin P
Biochimie. 1977;59(8-9):673-8. doi: 10.1016/s0300-9084(77)80245-9.
The reaction mechanism of erythrocyte phosphofructokinase (PFK) was investigated by the initial velocity and the product inhibition. Intersecting lines obtained with initial velocity studies are consistent with a sequential mechanism and the formation of ternary complex as an intermediate. The product inhibition studies support an ordered Bi Bi mechanism in which fructose 6 phosphate (F6P) is the first substrate binding and adenosine diphosphate (ADP) is dissociated from the enzyme before fructose-1,6-P2 (FDP).
通过初速度法和产物抑制法研究了红细胞磷酸果糖激酶(PFK)的反应机制。初速度研究得到的相交直线与序列机制以及三元复合物作为中间体的形成相一致。产物抑制研究支持有序的双双机制,其中6-磷酸果糖(F6P)是第一个结合的底物,并且在1,6-二磷酸果糖(FDP)之前二磷酸腺苷(ADP)从酶上解离。