Haveman J, Lavorel J
Biochim Biophys Acta. 1975 Dec 11;408(3):269-38. doi: 10.1016/0005-2728(75)90129-2.
After a 500 mus laser flash a 120 mus phase in the decay of delayed fluorescence is visible under a variety of circumstances in spinach chloroplasts and subchloroplast particles enriched in Photosystem II prepared by means of digitonin. The level of this phase is high in the case of inhibition of oxygen evolution at the donor side of Photosystem II. Comparison with the results of Babcock and Sauer (1975) Biochim. Bio-phys. Acta 376, 329-344, indicates that their EPR signal IIf which they suppose to be due to Z+, the oxidized first secondary donor of Photosystem II, is well correlated with a large amplitude of our 120 mus phase. We explain our 120 mus phase by the intrinsic back reaction of the excited reaction center in the presence of Z+, as predicted by Van Gorkom and Donze (1973) Photochem. Photobiol. 17, 333-342. The redox state of Z+ is dependent on the internal pH of the thylakoids. The results on the effect of pH in the mus region are compared with those obtained in the ms region.
在500微秒的激光闪光后,在多种情况下,菠菜叶绿体以及通过洋地黄皂苷制备的富含光系统II的亚叶绿体颗粒中,延迟荧光衰减过程中120微秒的相位清晰可见。在光系统II供体侧的氧释放受到抑制的情况下,该相位的水平较高。与巴布科克和绍尔(1975年,《生物化学与生物物理学报》376卷,329 - 344页)的结果相比较表明,他们认为是由于光系统II的第一个次级供体Z +氧化所致的电子顺磁共振信号IIf,与我们120微秒相位的大振幅密切相关。正如范戈尔科姆和唐泽(1973年,《光化学与光生物学》17卷,333 - 342页)所预测的那样,我们用在Z +存在下激发反应中心的固有逆反应来解释我们的120微秒相位。Z +的氧化还原状态取决于类囊体的内部pH值。将微秒区域内pH值影响的结果与毫秒区域内获得的结果进行了比较。