de Jonge P C, Westerhoff H V
Biochem J. 1982 May 15;204(2):515-23. doi: 10.1042/bj2040515.
The maximum redox potential difference between the NAD+/NADH couple and the succinate/fumarate couple generated during ATP-energized reduction of NAD+ by succinate in submitochondrial particles was measured, together with the electrochemical potential difference for protons (delta mu approximately H+). The presence of cyanide, the time-independence of the redox potential difference and the irrelevance of the initial redox state of the NAD+/NADH couple ensured that the experimental situation corresponded to a 'static-head condition' with delta mu approximately H+ as the input force and the redox potential difference as the output force, the flow of electrons having reached dynamic equilibrium. Consequently, the observed value of 1.6 for the ratio delta Ge/delta mu approximately H+ is interpreted as indicating that the leads to H+/e- stoicheiometry at 'site 1' is 1.5 and that therefore the mechanism of the proton pump at 'site 1' is not of the group-translocation type (no direct leads to e - leads to H+ coupling).
测量了在亚线粒体颗粒中琥珀酸使NAD⁺发生ATP驱动还原过程中,NAD⁺/NADH电对与琥珀酸/延胡索酸电对之间的最大氧化还原电位差,以及质子的电化学电位差(Δμₕ⁺)。氰化物的存在、氧化还原电位差与时间的无关性以及NAD⁺/NADH电对初始氧化还原状态的无关性,确保了实验情况对应于一种“静态水头条件”,其中Δμₕ⁺作为输入力,氧化还原电位差作为输出力,电子流已达到动态平衡。因此,观察到的ΔGₑ/Δμₕ⁺比值为1.6,这被解释为表明在“位点1”处H⁺/e⁻化学计量比为1.5,因此“位点1”处质子泵的机制不是基团转位类型(没有直接的e⁻→H⁺偶联)。