Williams N H, Yandell J K
Biochim Biophys Acta. 1985 Nov 27;810(2):274-7. doi: 10.1016/0005-2728(85)90142-2.
The kinetics and mechanism of the reduction of oxidized cytochrome c by ascorbate has been investigated in potassium nitrate, potassium 4-morpholineethanesulfonate (KMes), potassium sulfate and potassium ascorbate media. The results are consistent with simple second order electron transfer from ascorbate dianion to cytochrome c and do not support electron transfer from an ascorbate dianion bound to the protein of the cytochrome as recently proposed by Myer and Kumar. A rate constant of 8 X 10(5) M-1 X s-1 (25 degrees C, ionic strength, 0.1) was found for the electron-transfer step. This rate constant is essentially independent of the specific ions used in controlling ionic strength.
已在硝酸钾、4-吗啉乙磺酸钾(KMes)、硫酸钾和抗坏血酸钾介质中研究了抗坏血酸还原氧化型细胞色素c的动力学和机理。结果与抗坏血酸二价阴离子向细胞色素c的简单二级电子转移一致,并不支持迈尔和库马尔最近提出的从与细胞色素蛋白质结合的抗坏血酸二价阴离子进行电子转移的观点。发现电子转移步骤的速率常数为8×10⁵ M⁻¹·s⁻¹(25℃,离子强度0.1)。该速率常数基本上与用于控制离子强度的特定离子无关。