Department of Structural Chemistry and Biochemistry, The Weizmann Institute of Science, Rehovot, Israel.
Plant Physiol. 1978 Jul;62(1):1-5. doi: 10.1104/pp.62.1.1.
Photosystem II activity, development, and organization were studied in membranes from dark-adapted Euglena gracilis Klebs var. Z Pringsheim cells during a modulated greening process of light-dark-light cycles. The results obtained from measurements of overlapping partial photosystem II (PSII) reactions (fluorescence induction parameters, quantum yield, flash yield, and maximal rate of H(2)O --> 2,6-dichlorophenolindophenol [DCIP] and 1,5-diphenylcarbazide [DPC] --> DCIP reactions) during these cycles indicate the formation of active PSII units in the dark. The necessity for proteins from the chloroplast translational machinery for this formation is evidenced by the inhibition of synthesis of the PSII units in chloramphenicol-treated cells. The effect of this drug, both during the dark and second light periods, can be summarized as follows: (a) disruption of the electron transfer connection to the plastoquinone pool, or decrease in the pool size; (b) loss of excitation energy transfer efficiency in the second light period; (c) impairment of the O(2) evolution appratus, as shown by comparison of the efficiency of DCP and H(2)O as electron donors.These conclusions are based on the use of a previously developed method of measurement and analysis of data (Cahen et al. 1976 Plant Physiol 58: 257-267).
在光暗-光循环的调制绿化过程中,研究了暗适应的 Euglena gracilis Klebs var. Z Pringsheim 细胞的膜中的光系统 II 活性、发育和组织。通过测量重叠的部分光系统 II (PSII)反应(荧光诱导参数、量子产率、闪光产率以及 H2O 到 2,6-二氯苯酚吲哚酚 [DCIP] 和 1,5-二苯基卡巴肼 [DPC] 到 DCIP 反应的最大速率)得到的结果表明,在黑暗中形成了活性 PSII 单位。这一形成需要来自叶绿体翻译机制的蛋白质,这一点可以通过氯苯丙氨酸处理的细胞中 PSII 单位合成的抑制来证明。这种药物在暗期和第二期光照期的影响可以概括如下:(a) 破坏电子传递到质体醌库的连接,或库大小减小;(b) 在第二期光照期内,激发能量转移效率丧失;(c) O2 释放装置受损,这可以通过比较 DCP 和 H2O 作为电子供体的效率来证明。这些结论是基于以前开发的测量和数据分析方法(Cahen 等人,1976 年《植物生理学》58:257-267)得出的。