Maeda-Yorita K, Aki K
J Biochem. 1984 Sep;96(3):683-90. doi: 10.1093/oxfordjournals.jbchem.a134886.
The effect of NAD+ on lipoamide dehydrogenase from pig heart was investigated physicochemically. The observed and theoretical oxidation-reduction mid-point potentials for the oxidized lipoamide dehydrogenase (E)/two-electron-reduced lipoamide dehydrogenase (EH2) couple in the presence on NAD+ were -218 mV and -251 mV, respectively, at pH 6.0. Therefore, unexpectedly the mid-point potential of the enzyme became more positive on NAD+ binding. Decreases in the fluorescence lifetime and intensity and increase in the degree of polarization of enzyme-bound FAD were observed in the presence of NAD+. Fluorescence quenching of bound FAD by NAD+ was released by phenobarbital. The results suggest that NAD+ strengthens the intramolecular dynamic interaction between the isoalloxazine moiety and adenine moiety of bound FAD, and so alters the mid-point potential of the enzyme. These findings indicate that NAD+ acts not only as an acceptor of electrons from EH2, but also as an effector in the flavin-disulfide interaction of EH2.
采用物理化学方法研究了NAD⁺对猪心脂酰胺脱氢酶的影响。在pH 6.0条件下,存在NAD⁺时,氧化型脂酰胺脱氢酶(E)/双电子还原型脂酰胺脱氢酶(EH₂)偶联的实测氧化还原中点电位和理论氧化还原中点电位分别为-218 mV和-251 mV。因此,出乎意料的是,酶的中点电位在结合NAD⁺后变得更正。在存在NAD⁺的情况下,观察到酶结合的FAD的荧光寿命和强度降低,偏振度增加。苯巴比妥可解除NAD⁺对结合FAD的荧光猝灭。结果表明,NAD⁺增强了结合FAD的异咯嗪部分和腺嘌呤部分之间的分子内动态相互作用,从而改变了酶的中点电位。这些发现表明,NAD⁺不仅作为EH₂的电子受体,还作为EH₂黄素二硫键相互作用中的效应物。