Iushchishina A N, Genkin M V, Koroteev S V, Malievskiĭ A D, Davydov R M
Mol Biol (Mosk). 1988 Nov-Dec;22(6):1650-7.
To model the effect of membrane environment on the electron transfer reactions we studied the thermodynamics and kinetics of the reactions of cytochrome c and 2,6-dichlorophenolindophenol with ferri- and ferrocyanide in the reversed micelles cetyltrimethylammonium bromide in chloroform/octan mixture. Incorporation of the protein in micelles leads to increasing the equilibrium constant (K1) up to 300 times. This effect is mainly due to a decrease in the ferrocytochrome c oxidation rate constant in the reaction with ferricyanide. Micellar solubilization of the dye also leads to a marked increase in the equilibrium constant K2. The estimations of the values K1 and K2 in water-alcohol mixtures and in aqueous micellar solutions of surfactant together with kinetical and spectral data show that the increase of K1 and K2 in reversed micelles is caused generally by redox potential changes of low-molecular reagents. The latter change their environment after adsorption on the micellar surface.
为了模拟膜环境对电子转移反应的影响,我们研究了细胞色素c和2,6 - 二氯酚靛酚与铁氰化物和亚铁氰化物在氯仿/辛烷混合物中的十六烷基三甲基溴化铵反胶束中的反应热力学和动力学。蛋白质掺入胶束导致平衡常数(K1)增加高达300倍。这种效应主要是由于亚铁细胞色素c与铁氰化物反应的氧化速率常数降低。染料的胶束增溶作用也导致平衡常数K2显著增加。在水 - 醇混合物和表面活性剂的水性胶束溶液中对K1和K2值的估计以及动力学和光谱数据表明,反胶束中K1和K2的增加通常是由低分子试剂的氧化还原电位变化引起的。后者在吸附到胶束表面后改变了它们的环境。