Wagner R, Junge W
Biochim Biophys Acta. 1977 Nov 17;462(2):259-72. doi: 10.1016/0005-2728(77)90124-4.
The membrane bound coupling factor of photophosphorylation is studied after pretreatment of broken chloroplasts with the bifunctional N,N-orthophenyldimaleimide under energization of the thylakoid membrane by mild flashing light. The proton conduction of the membrane is monitored both via the electrochromic absorption changes and via selective pH-indicating dyes. It is found that the coupling factor, after interaction with N,N-orthophenyldimaleimide during the preillumination period, shortcircuits one of the two protons pumped inside after excitation of chloroplasts with one short flash of light. In contrast to the low proton conductivity of the unperturbed thylakoid membrane (relaxation time for a proton gradient greater than 5s), this extra proton channel leads to a partial relaxation of a proton gradient within a few ms. Although limited to only one proton per electron, this extra proton conducting pathway is not otherwise specific. It operates with protons resulting from both Photosystem I and Photosystem II activity. In addition it operates with protons already present in the internal phase before firing of the exciting light flash. These effects are prevented by the presence of ATP (but not GTP) during the preillumination period. It is suggested that the modified coupling factor is gated open by the light induced electric field across the thylakoid membrane while self closing after passage of one proton per activated coupling factor.
在用双功能N,N-邻苯基马来酰亚胺预处理破碎的叶绿体后,在类囊体膜通过温和闪光激发的情况下,研究了光磷酸化的膜结合偶联因子。通过电致变色吸收变化和选择性pH指示染料监测膜的质子传导。结果发现,在预照光期间与N,N-邻苯基马来酰亚胺相互作用后,偶联因子使叶绿体经一次短闪光激发后泵入内部的两个质子之一发生短路。与未受干扰的类囊体膜的低质子传导率(质子梯度的弛豫时间大于5秒)相反,这种额外的质子通道导致质子梯度在几毫秒内部分弛豫。尽管每个电子仅限制一个质子,但这种额外的质子传导途径并无其他特异性。它对来自光系统I和光系统II活性产生的质子均起作用。此外,它对激发闪光之前已经存在于内部相中质子也起作用。预照光期间存在ATP(而非GTP)可防止这些效应。有人提出,修饰后的偶联因子在类囊体膜上的光诱导电场作用下门控打开,而每个活化的偶联因子通过一个质子后会自行关闭。