Niehaus W G, Richardson S B, Wolz R L
Department of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg 24061-0308, USA.
Arch Biochem Biophys. 1996 Sep 15;333(2):333-7. doi: 10.1006/abbi.1996.0399.
6-Phosphogluconate dehydrogenase (EC 1.1.1.44) has been purified from Cryptococcus neoformans, an encapsulated yeast that is an opportunistic pathogen of AIDS patients. The dimeric enzyme had a subunit molecular weight of 50,000, a specific activity of 50 units mg-1, and Km values of 13 microM for 6-phosphogluconate and 0.89 microM for NADP. This enzyme, like many fungal dehydrogenases, was inhibited by Zn2+, with the inhibition pattern being competitive versus the nonnucleotide substrate. In the presence of micromolar Zn2+, the reaction was biphasic, with the reduction of NADP proceeding initially at the control rate, but, over the time course of 20-300 s, this initial nonlinear phase reached a final, linear steady state with a slower velocity. This pattern is indicative of a slow binding inhibition process, for which we have calculated the following kinetic constants: k6, the limiting rate constant for the transition from initial to final steady state was 0.0024 s-1, corresponding to a half-time of 300 s; Ki*, the overall equilibrium constant for the dissociation of E*Zn2+ to E + Zn2+ was 0.021 microM.
已从新型隐球菌中纯化出6-磷酸葡萄糖酸脱氢酶(EC 1.1.1.44),新型隐球菌是一种有荚膜的酵母,是艾滋病患者的机会性病原体。该二聚体酶的亚基分子量为50,000,比活性为50单位mg-1,对6-磷酸葡萄糖酸的Km值为13 microM,对NADP的Km值为0.89 microM。与许多真菌脱氢酶一样,该酶受Zn2+抑制,抑制模式为与非核苷酸底物竞争。在微摩尔浓度的Zn2+存在下,反应呈双相,NADP的还原最初以对照速率进行,但在20-300 s的时间进程中,这个初始的非线性阶段达到最终的线性稳态,速度较慢。这种模式表明是一个慢结合抑制过程,我们已计算出以下动力学常数:k6,从初始稳态转变为最终稳态的极限速率常数为0.0024 s-1,对应半衰期为300 s;Ki*,E*Zn2+解离为E + Zn2+的总平衡常数为0.021 microM。