Schmid G H, Menke W, Koenig F, Radunz A
Z Naturforsch C Biosci. 1976 May-Jun;31(5-6):304-11. doi: 10.1515/znc-1976-5-616.
A polypeptide fraction with the apparent molecular weight 11 000 was isolated from stroma-freed chloroplasts from Anthirrhinum majus. An antiserum to this polypeptide fraction inhibits photosynthetic electron transport in chloroplasts from Nicotiana tabacum. The relative degree of inhibition is pH dependent and has its maximum at pH 7.4. The maximal inhibition observed was 93%. The dependence of the inhibition on the amount of antiserum yields a sigmoidal curve which hints at a cooperative effect. A calculation of the Hill interaction coefficient gave the value of 10. The inhibition occurs on the water splitting side of photosystem II between the sites of electron donation of tetramethyl benzidine and diphenylcarbazide. Tetramethyl benzidine donates its electrons before the site where diphenylcarbazide feeds in its electrons. Analysis of the steady state level of the variable fluorescence also indicates that the inhibition site is on the water splitting side of photosystem II. Tris-washed chloroplasts are equally inhibited by the antiserum and the inhibition is also observed in the presence of an inhibitor of photophosphorylation like dicyclohexyl carbodiimide and in the presence of the uncoupler carbonylcyanide m-chlorophenyl hydrazone (CCCP) which means that the inhibitory action is directed towards the electron transport chain. Valinomycin which is supposed to affect the cation permeability of the thylakoid membrane has no influence on the inhibitory action of the antiserum. The same is valid for gramicidin. Methylamine on the other hand can induce a state in the thylakoids in which the antiserum is not effective. If the antibodies are already adsorbed prior to the methylamine addition then the high inhibitory effect by the antiserum remains unchanged upon addition of methylamine. From the experiments it follows that a component from the vicinity of photosystem II is accessible to antibodies that is, the component is located in the outer surface of the thylakoid membrane. It appears that the inhibitory effect is produced in the course of the light reaction.
从金鱼草无基质的叶绿体中分离出一种表观分子量为11000的多肽组分。针对该多肽组分的抗血清可抑制烟草叶绿体中的光合电子传递。抑制的相对程度依赖于pH,在pH 7.4时达到最大值。观察到的最大抑制率为93%。抑制作用对抗血清量的依赖性产生一条S形曲线,这暗示存在协同效应。希尔相互作用系数的计算值为10。抑制作用发生在光系统II的水裂解侧,位于四甲基联苯胺和二苯卡巴肼电子供体位点之间。四甲基联苯胺在二苯卡巴肼供入电子的位点之前供出其电子。对可变荧光稳态水平的分析也表明抑制位点在光系统II的水裂解侧。经Tris洗涤的叶绿体同样受到抗血清的抑制,并且在存在光磷酸化抑制剂如二环己基碳二亚胺以及解偶联剂羰基氰化物间氯苯腙(CCCP)的情况下也观察到抑制作用,这意味着抑制作用针对的是电子传递链。据认为会影响类囊体膜阳离子通透性的缬氨霉素对抗血清的抑制作用没有影响。短杆菌肽也是如此。另一方面,甲胺可诱导类囊体进入一种抗血清无效的状态。如果在添加甲胺之前抗体就已被吸附,那么添加甲胺后抗血清的高抑制效果保持不变。从这些实验可以得出,光系统II附近的一个组分可被抗体识别,也就是说,该组分位于类囊体膜的外表面。抑制作用似乎是在光反应过程中产生的。