Grebanier A E, Jagendorf A T
Biochim Biophys Acta. 1977 Jan 6;459(1):1-9. doi: 10.1016/0005-2728(77)90002-0.
The irreversible inhibition of chloroplast phosphorylation by either sulfate anions, or N-ethylmaleimide, is energy dependent. Chloroplasts must first be illuminated in the presence of the inhibitors and a mediator of electron flow, for the subsequent phosphorylation to show any inhibition. Both inhibitors affect the chloroplast coupling factor 1. Electron transport only through Photosystem I can be used to activate either of these inhibitions. The subsequent inhibition in a second light reaction is the same whether ATP synthesis is supported by Photosystem I, or by Photosystem II electron transport. The reverse experiment, activating inhibition by electron transport only through Photosystem II, is possible in the case of sulfate. Again, the inhibition is expressed whether Photosystem II or Photosystem I electron flow supports ATP synthesis. We conclude that the two electron transport regions of probably generate the same high energy state which is able to activate all members of a functionally uniform coupling factor population. These enzyme molecules must catalyze phosphorylation coupled to electron transport through either region of the chain. The results tend to discredit models requiring a separate group of coupling factor molecules unique to each part of the chain.
硫酸根阴离子或N - 乙基马来酰亚胺对叶绿体磷酸化的不可逆抑制是能量依赖性的。叶绿体必须首先在抑制剂和电子流介导物存在的情况下被光照,以便随后的磷酸化表现出任何抑制作用。两种抑制剂都影响叶绿体偶联因子1。仅通过光系统I的电子传递可用于激活这些抑制作用中的任何一种。无论ATP合成是由光系统I还是光系统II电子传递支持,在第二次光反应中的后续抑制作用都是相同的。在硫酸根的情况下,通过仅通过光系统II的电子传递来激活抑制作用的反向实验是可行的。同样,无论光系统II还是光系统I电子流支持ATP合成,抑制作用都会表现出来。我们得出结论,两个电子传递区域可能产生相同的高能状态,该高能状态能够激活功能上统一的偶联因子群体的所有成员。这些酶分子必须催化与通过链的任一区域的电子传递偶联的磷酸化。这些结果倾向于质疑那些需要为链的每个部分配备一组独特的单独偶联因子分子的模型。