van Dijk C, Veeger C
Eur J Biochem. 1981 Feb;114(2):209-19. doi: 10.1111/j.1432-1033.1981.tb05138.x.
The effects of temperature on the ionization constant (pK') and apparent midpoint potential (EB) of the unprotonated species of Megasphaera elsdenii flavodoxin hydroquinone shows that, above 15 degrees C, delta pK' . K-1 = -9.7 X 10(-3) and delta EB . K-1 = -0.6 mV. The effects of pH and redox potential on the hydrogen production activity with fixed concentrations of methyl viologen semiquinone (0.3 mM; artificial donor) and M. elsdenii flavodoxin hydroquinone (50 microM; natural donor) show that with decreasing pH the activity increases. Irrespective of the pH and electron donor, at increasing redox potential, a redox-potential-independent production activity is followed by a redox-potential-dependent production activity. This redox-potential-dependent behaviour of the hydrogen production activity represents an n = 2-type of redox titration curve with an 'apparent midpoint potential' which corresponds with the potential of the hydrogen electrode at that pH. The effect of pH on the manometrically determined hydrogen production activity (direct) is in good agreement with that determined spectrophotometrically (indirect; see preceding paper), with both electron donors tested. In contrast to predictions from the models for hydrogenase activity [van Dijk et al. (1980) Eur. J. Biochem.102, 317--330], a double-reciprocal plot of the kinetic data for M. elsdenii flavodoxin hydroquinone at pH 5.5 is non-linear. A slightly adapted kinetic model based on a similar mathematical formulation of its rate equation, to explain the effects of redox potential, proton and electron (donor) concentration on the hydrogenase activity is proposed. This model also explains, on a theoretical basis, the effects of pH and redox potential on the hydrogen production activity. The effect of pH on the hydrogen oxidation activity with methyl viologen and benzyl viologen as electron acceptors shows for both dyes an optimum at pH 9.7. The ratio of the activities with both viologens is constant over the ph range tested.
温度对埃氏巨球型菌黄素氧还蛋白对苯二酚未质子化物种的电离常数(pK')和表观中点电位(EB)的影响表明,在15摄氏度以上,ΔpK'.K-1 = -9.7×10(-3) 且ΔEB.K-1 = -0.6毫伏。在固定浓度的甲基紫精半醌(0.3毫摩尔;人工供体)和埃氏巨球型菌黄素氧还蛋白对苯二酚(50微摩尔;天然供体)条件下,pH值和氧化还原电位对产氢活性的影响表明,随着pH值降低,活性增加。无论pH值和电子供体如何,随着氧化还原电位升高,产氢活性先是与氧化还原电位无关,随后变为与氧化还原电位有关。产氢活性的这种与氧化还原电位有关的行为代表了一种n = 2型的氧化还原滴定曲线,其“表观中点电位”与该pH值下氢电极的电位相对应。pH值对测压法测定的产氢活性(直接)的影响与分光光度法测定的结果(间接;见前文)非常吻合,两种电子供体均如此。与氢化酶活性模型的预测结果[范·迪克等人(1980年)《欧洲生物化学杂志》102, 317 - 330]相反,pH值为5.5时埃氏巨球型菌黄素氧还蛋白对苯二酚动力学数据的双倒数图是非线性的。提出了一个基于其速率方程类似数学公式的略微调整的动力学模型,以解释氧化还原电位、质子和电子(供体)浓度对氢化酶活性的影响。该模型还从理论上解释了pH值和氧化还原电位对产氢活性的影响。以甲基紫精和苄基紫精作为电子受体时,pH值对氢氧化活性的影响表明,两种染料在pH值为9.7时均出现最佳值。在所测试的pH范围内,两种紫精的活性比值是恒定的。