McCray J A, Kihara T
Biochim Biophys Acta. 1979 Nov 8;548(2):417-26. doi: 10.1016/0005-2728(79)90145-2.
The oxidation of reduced cytochrome c by ferricyanide has been studied over a wide range of ferricyanide concentrations using a continuous-flow apparatus. The formation of a ferrocytochrome c-ferricyanide complex has been demonstrated and the binding and electron transfer processes separated to give both the oxidation electron transfer rate and the binding rate parameters. The electron transfer rate has been found to be 1.86 . 10(3) s-1 in H2O buffer and 1.36 . 10(3) s-1 in 2H2O demonstrating that a deuterium isotope effect of similar magnitude (R = 1.37) to that found in the cytochrome reactions in photosynthetic bacteria [18] is also found in the reaction studied here. The binding association rate parameters also show a similar deuterium isotope effect suggesting that water rotation may be involved in both the binding of ferricyanide to reduced cytochrome c and the subsequent oxidation electron transfer.
使用连续流动装置,在广泛的铁氰化物浓度范围内研究了铁氰化物对还原型细胞色素c的氧化作用。已证明形成了亚铁细胞色素c - 铁氰化物复合物,并将结合和电子转移过程分开,以给出氧化电子转移速率和结合速率参数。已发现电子转移速率在H2O缓冲液中为1.86×10³ s⁻¹,在2H2O中为1.36×10³ s⁻¹,这表明在此研究的反应中也发现了与光合细菌中细胞色素反应中发现的类似大小的氘同位素效应(R = 1.37)。结合缔合速率参数也显示出类似的氘同位素效应,表明水的旋转可能参与铁氰化物与还原型细胞色素c的结合以及随后的氧化电子转移。