Kobayashi Y, Inoue Y, Shibata K
Biochim Biophys Acta. 1976 Sep 13;440(3):600-8. doi: 10.1016/0005-2728(76)90045-1.
The photosystem-II activity of chloroplasts was inhibited by the treatment with p-nitrothiophenol (NphSH) in the light, and the inhibition was accompanied by a change of the fluorescence spectrum. Aromatic mercaptans examined were active in causing this inhibition and fluorescence change. These effects of p-nitrothiophenol were highly accelerated by blocking the electron transport of the oxidation side of photosystem II by carbonyl-cyanide-m-chlorophenylhydrazone (CCCP) or Tris-HC1 or heat pre-treatment, whereas these were suppressed by blocking the transport on the reduction side by 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU). It was deduced that the site of NphSH action in the electron transport chain is closer to the reaction center of photosystem II that the blocking site of CCCP or Tris-HC1 or heat, and that such a site in photosystem II is exposed to be modified with NphSH when electron carriers on the oxidation side of photosystem II are oxidized by illumination.
在光照条件下,用对硝基硫酚(NphSH)处理会抑制叶绿体的光系统II活性,这种抑制伴随着荧光光谱的变化。所检测的芳香族硫醇在引起这种抑制和荧光变化方面具有活性。羰基氰化物间氯苯腙(CCCP)、Tris-HCl或热预处理通过阻断光系统II氧化侧的电子传递,极大地加速了对硝基硫酚的这些效应,而通过3-(3,4-二氯苯基)-1,1-二甲基脲(DCMU)阻断还原侧的电子传递则抑制了这些效应。据推断,NphSH在电子传递链中的作用位点比CCCP、Tris-HCl或热的阻断位点更靠近光系统II的反应中心,并且当光系统II氧化侧的电子载体被光照氧化时,光系统II中的这样一个位点会暴露出来,从而被NphSH修饰。