Centro di Studio CNR sulla Biologia Cellulare e Molecolare delle Piante, Dipartimento di Biologia, Università di Milano, Via Celoria, 26, 20133, Milano, Italy.
Photosynth Res. 1995 Jan;46(3):379-92. doi: 10.1007/BF00032292.
Photosystem 2 photochemical efficiency, measured as the rate of Qa reduction, was observed to be inhibited by preillumination with single turnover flashes, whilst Fo and Fm were not affected. Such inhibition was reversed by the uncoupler nigericin or by incubating the thylakoids in the dark for ca. 2 min after the preillumination. The presence of ATP in micromolar concentrations increased the time of dark recovery from the inhibition. The inhibition of fluorescence rise was not changed when 70% of the excitation energy available in the antenna was quenched by dinitrobenzene. Quantitative analysis of the observed fluorescence induction indicates that this phenomenon is due to the inhibition of the photochemical reaction itself. Uncouplers such NH4Cl were unable to reverse the inhibition and only a few flashes of saturating intensity (10 or less) were required for the onset of it. This suggests that protons localised in domains rather than a pH gradient between the thylakoid lumen bulk solution and the external one are involved in this regulation of PS 2 efficiency.
光系统 2 光化学效率,以 Qa 还原的速率来衡量,被观察到会受到单 turnover 闪光预照射的抑制,而 Fo 和 Fm 不受影响。这种抑制可以通过解偶联剂 Nigericin 或在预照射后将类囊体在黑暗中孵育约 2 分钟来逆转。在微摩尔浓度存在 ATP 时,从抑制中恢复的黑暗时间增加。当通过二硝基苯醌猝灭天线中可用的激发能量的 70%时,荧光上升的抑制没有改变。对观察到的荧光诱导的定量分析表明,这种现象是由于光化学反应本身的抑制所致。解偶联剂如氯化铵无法逆转抑制作用,并且仅需要 10 个或更少的饱和强度闪光(10 个或更少)即可开始抑制作用。这表明质子定位于域中,而不是类囊体腔的质体醌和外部之间的 pH 梯度,参与了 PS 2 效率的这种调节。