Hangarter R P, Grandoni P, Ort D R
Department of Plant Biology, United States Department of Agriculture/ARS, University of Illinois, Urbana 61801.
J Biol Chem. 1987 Oct 5;262(28):13513-9.
There are two separate aspects to the energetic control over the initiation of ATP formation by chloroplast thylakoid membranes: (i) the free energy requirement for the phosphorylation of ADP and (ii) the energy-dependent transformation of the coupling factor into a catalytically active state. Using flash excitation, we have been able to distinguish between limitations imposed on ATP formation by the energetics of coupling factor activation from limitations imposed by the thermodynamics of ADP phosphorylation. We have placed particular emphasis on the effects of coupling factor reduction. ATP hydrolysis, ATP synthesis, and the release of tightly bound [14C]ADP were initiated by fewer flashes in thylakoid membranes in which the coupling factors were prereduced than in membrane samples in which the coupling factor remained oxidized. Only under conditions in which ATP synthesis occurred against a large chemical potential (i.e. delta GATP) did the onset of net ATP synthesis require a larger electrochemical potential than did the activation of the coupling factor. Thus, only at delta GATP values greater than about 51 kJ.mol-1 for thylakoid membranes with oxidized coupling factors and about 45 kJ.mol-1 when the coupling factors are reduced was the onset of ATP synthesis dictated by the thermodynamic equilibrium between ATP and ADP. At lower delta GATP values, the electrochemical potential became energetically adequate to phosphorylate ADP prior to becoming adequate to activate the coupling factor. These data indicate that reduction of the coupling factor lowers the delta pH necessary for activation from approximately 2.9 to approximately 2.6 units. Accompanying the lower energetic requirement for the activation of the reduced coupling factor was an increase in the efficiency of ATP synthesis under conditions of limiting energization.
叶绿体类囊体膜对ATP形成起始的能量控制有两个独立的方面:(i)ADP磷酸化所需的自由能,以及(ii)偶联因子向催化活性状态的能量依赖性转变。利用闪光激发,我们能够区分偶联因子活化的能量学对ATP形成的限制与ADP磷酸化的热力学所施加的限制。我们特别强调了偶联因子还原的影响。与偶联因子保持氧化的膜样品相比,在偶联因子预先还原的类囊体膜中,引发ATP水解、ATP合成以及紧密结合的[14C]ADP释放所需的闪光次数更少。只有在ATP合成是逆着较大化学势(即ΔGATP)进行的条件下,净ATP合成的起始才需要比偶联因子活化更大的电化学势。因此,对于偶联因子氧化的类囊体膜,只有在ΔGATP值大于约51 kJ·mol-1时,以及偶联因子还原时约为45 kJ·mol-1时,ATP合成的起始才由ATP和ADP之间的热力学平衡决定。在较低的ΔGATP值下,电化学势在能量上足以使ADP磷酸化,然后才足以激活偶联因子。这些数据表明,偶联因子的还原将激活所需的ΔpH从约2.9单位降低到约2.6单位。伴随着还原型偶联因子活化所需能量的降低,在能量供应受限的条件下,ATP合成效率有所提高。