Axley M J, Grahame D A
Laboratory of Biochemistry, National Heart, Lung, and Blood Institute, National Insitute of Health, Bethesda, Maryland 20892.
J Biol Chem. 1991 Jul 25;266(21):13731-6.
Kinetic parameters of the selenium-containing, formate dehydrogenase component of the Escherichia coli formate-hydrogenlyase complex have been determined with purified enzyme. A ping-pong Bi Bi kinetic mechanism was observed. The Km for formate is 26 mM, and the Km for the electron-accepting dye, benzyl viologen, is in the range 1-5 mM. The maximal turnover rate for the formate-dependent catalysis of benzyl viologen reduction was calculated to be 1.7 x 10(5) min-1. Isotope exchange analysis showed that the enzyme catalyzes carbon exchange between carbon dioxide and formate in the absence of other electron acceptors, confirming the ping-pong reaction mechanism. Dissociation constants for formate (12.2 mM) and CO2 (8.3 mM) were derived from analysis of the isotope exchange data. The enzyme catalyzes oxidation of the alternative substrate deuterioformate with little change in the Vmax, but the Km for deuterioformate is approximately three times that of protioformate. This implies formate oxidation is not rate-limiting in the overall coupled reaction of formate oxidation and benzyl viologen reduction. The deuterium isotope effect on Vmax/Km was observed to be approximately 4.2-4.5. Sodium nitrate was found to inhibit enzyme activity in a competitive manner with respect to formate, with a Ki of 7.1 mM. Sodium azide is a noncompetitive inhibitor with a Ki of about 80 microM.
利用纯化的酶测定了大肠杆菌甲酸-氢裂解酶复合物中含硒的甲酸脱氢酶组分的动力学参数。观察到一种乒乓双底物双产物动力学机制。甲酸的米氏常数(Km)为26 mM,电子受体染料苄基紫精的Km在1-5 mM范围内。计算得出,依赖甲酸催化苄基紫精还原的最大周转速率为1.7×10⁵ min⁻¹。同位素交换分析表明,该酶在没有其他电子受体的情况下催化二氧化碳和甲酸之间的碳交换,证实了乒乓反应机制。通过对同位素交换数据的分析得出甲酸(12.2 mM)和二氧化碳(8.3 mM)的解离常数。该酶催化替代底物氘代甲酸的氧化,最大反应速率(Vmax)变化不大,但氘代甲酸的Km约为甲酸的三倍。这意味着在甲酸氧化和苄基紫精还原的整体偶联反应中,甲酸氧化不是限速步骤。观察到氘同位素对Vmax/Km的影响约为4.2-4.5。发现硝酸钠以与甲酸竞争的方式抑制酶活性,抑制常数(Ki)为7.1 mM。叠氮化钠是一种非竞争性抑制剂,Ki约为80 μM。