Sevostyanova Irina A, Yurshev Vladimir A, Solovjeva Olga N, Zabrodskaya Svetlana V, Kochetov German A
A.N. Belozersky Institute of Physico-Chemical Biology, Moscow State University, Moscow 119992, Russia.
Proteins. 2008 May 1;71(2):541-5. doi: 10.1002/prot.21880.
The effect of the type of the cation cofactor of transketolase (i.e., Ca2+ or Mg2+) on its interaction with xylulose 5-phosphate (donor substrate) has been studied. In the presence of magnesium, the active centers of the enzyme were functionally equivalent with respect to xylulose 5-phosphate binding and exhibited identical affinities for the donor substrate. Substitution of Ca2+ for Mg2+ results in the loss of the equivalence. In particular, this becomes apparent on binding of xylulose 5-phosphates to one of the two active centers of the enzyme, which caused the second center to undergo a several fold decrease in the affinity for the donor substrate.
已对转酮醇酶的阳离子辅因子类型(即Ca2+或Mg2+)对其与5-磷酸木酮糖(供体底物)相互作用的影响进行了研究。在镁存在的情况下,就5-磷酸木酮糖结合而言,该酶的活性中心在功能上是等效的,并且对供体底物表现出相同的亲和力。用Ca2+替代Mg2+会导致等效性丧失。特别是,当5-磷酸木酮糖与该酶的两个活性中心之一结合时,这一点变得很明显,这会导致第二个中心对供体底物的亲和力下降几倍。