Jensen B D, Gunter K K, Gunter T E
Arch Biochem Biophys. 1986 Jul;248(1):305-23. doi: 10.1016/0003-9861(86)90427-3.
In the accompanying article (T.E. Gunter and B.D. Jensen, 1986 Arch. Biochem. Biophys. 248, 289-304), a method is described for measuring the efficiencies of individual steps of the process of oxidative phosphorylation. The results of applying this method to the case of state 3 phosphorylation in rat liver mitochondria are reported here. The rate of energy use (or power use) at the gradient generation, leakage, and phosphorylation steps are reported as efficiencies and energy use factors in tabular form. The limits of the degrees of coupling of the gradient generation and phosphorylation steps are also determined and under the current conditions of measurement these degrees of coupling are found to be quite close to unity. The data can be used to show that the only sets of the stoichiometric parameters noH (the charge/2e- ratio in this case from succinate to oxygen), nPH (the H+/ATP ratio), and nTH (number of protons translocated during substrate-product transport) which are simultaneously consistent with both the laws of thermodynamics and with the current data are 8, 3, 1, and 6, 3, 0. The The efficiency of the phosphorylation step which is independent of noH and nTH averages 80% for the control data analyzed. If noH is 8 (succinate to oxygen), the average value of the efficiency of generation of the electrochemical proton gradient is approximately 91 percent. Since very little power (energy) would then be left over to be coupled in parallel to phosphorylation through some other means of coupling, this would place the electrochemical proton gradient in the direct path of power flow and identify it as "an" intermediate in the process. This would suggest that any other intermediate should be considered as being "in series" with the electrochemical proton gradient. The agents butyrate and propionate have been employed to permit investigation over a range of pH gradient and membrane potential. Both butyrate and propionate decrease the efficiency of generation of the electrochemical proton gradient and increase proton leakage. In addition, butyrate activates electron transport whereas propionate inhibits it. By using butyrate to modify the values of pH gradient and membrane potential, it can be shown that the ratio of the efficiency with which the pH gradient is used in phosphorylation to that with which the membrane potential is used is 1.08 +/- 0.38.
在随附的文章中(T.E. 冈特和B.D. 詹森,1986年,《生物化学与生物物理学报》248卷,289 - 304页),描述了一种测量氧化磷酸化过程中各个步骤效率的方法。本文报告了将该方法应用于大鼠肝线粒体状态3磷酸化情况的结果。梯度生成、泄漏和磷酸化步骤的能量使用速率(或功率使用速率)以表格形式报告为效率和能量使用因子。还确定了梯度生成和磷酸化步骤的耦合程度极限,发现在当前测量条件下,这些耦合程度非常接近1。这些数据可用于表明,唯一同时符合热力学定律和当前数据的化学计量参数组noH(在这种情况下,从琥珀酸到氧气的电荷/2e - 比率)、nPH(H⁺/ATP比率)和nTH(底物 - 产物转运过程中转运的质子数)分别为8、3、1和6、3、0。对于所分析的对照数据,与noH和nTH无关的磷酸化步骤效率平均为80%。如果noH为8(琥珀酸到氧气),电化学质子梯度生成效率的平均值约为91%。由于那时几乎没有剩余能量通过其他耦合方式与磷酸化并行耦合,这将使电化学质子梯度处于能量流动的直接路径,并将其确定为该过程中的“一种”中间体。这表明任何其他中间体都应被视为与电化学质子梯度“串联”。已使用丁酸盐和丙酸盐来研究在一系列pH梯度和膜电位范围内的情况。丁酸盐和丙酸盐都降低了电化学质子梯度的生成效率并增加了质子泄漏。此外,丁酸盐激活电子传递,而丙酸盐抑制电子传递。通过使用丁酸盐改变pH梯度和膜电位的值,可以表明pH梯度用于磷酸化的效率与膜电位用于磷酸化的效率之比为1.08±0.38。