Fork D C, Herbert S K, Malkin S
Department of Plant Biology, Carnegie Institution of Washington, Stanford, California 94305.
Plant Physiol. 1991 Mar;95(3):731-9. doi: 10.1104/pp.95.3.731.
The brown alga Macrocystis pyrifera (giant kelp) was studied by a combination of fluorescence spectroscopy at 77 kelvin, room temperature modulated fluorimetry, and photoacoustic techniques to determine how light energy is partitioned between photosystems I and II in states 1 and 2. Preillumination with farred light induced the high fluorescence state (state 1) as determined by fluorescence emission spectra measured at 77K and preillumination with green light produced a low fluorescence state (state 2). Upon transition from state 1 to state 2, there was an almost parallel decrease of all of the fluorescence bands at 693, 705, and 750 nanometers and not the expected decrease of fluorescence of photosystem II and increase of fluorescence in photosystem I. The momentary level of room temperature fluorescence (fluorescence in the steady state, F(s)), as well as the fluorescence levels corresponding to all closed (F(m)) or all open (F(o)) reaction-center states were measured following the kinetics of the transition between states 1 and 2. Calculation of the distribution of light 2 (540 nanometers) between the two photosystems was done assuming both the ;separate package' and ;spill-over' models. Unlike green plants, red algae, and cyanobacteria, the changes here of the light distribution were rather small in Macrocystis so that there was approximately an even distribution of the photosystem II light at 540 nanometers to photosystem I and photosystem II in both states 1 and 2. Photoacoustic measurements confirmed the conclusions reached as a result of fluorescence measurements, i.e. an almost equal distribution of light-2 quanta to both photosystems in each state. This conclusion was reached by analyzing the enhancement phenomenon by light 2 of the energy storage measured in far red light. The effect of light 1 in decreasing the energy storage measured in light 2 is also consistent with this conclusion. The photoacoustic experiments showed that there was a significant energy storage in light 1 which could be explained by cyclic electron transport around photosystem I. From a quantitative analysis of the enhancement effect of background light 2 (maximum enhancement of 1.4-1.5) it was shown that around 70% of light 1 was distributed to this cyclic photosystem I transport.
采用77K荧光光谱、室温调制荧光法和光声技术相结合的方法,对褐藻巨藻进行了研究,以确定在状态1和状态2下光能是如何在光系统I和光系统II之间分配的。用远红光预照射诱导产生高荧光状态(状态1),这是通过在77K下测量的荧光发射光谱确定的,而用绿光预照射则产生低荧光状态(状态2)。从状态1转变为状态2时,693、705和750纳米处所有荧光带几乎同时下降,而不是光系统II荧光预期的下降和光系统I荧光的增加。在状态1和状态2之间转变的动力学过程之后,测量了室温荧光的瞬时水平(稳态荧光,F(s)),以及对应于所有关闭(F(m))或所有开放(F(o))反应中心状态的荧光水平。假设“独立包”和“溢出”模型,计算了两个光系统之间光2(540纳米)的分布。与绿色植物、红藻和蓝细菌不同,巨藻中光分布的变化相当小,因此在状态1和状态2下,540纳米处光系统II的光大致均匀地分布在光系统I和光系统II之间。光声测量证实了荧光测量得出的结论,即在每个状态下光2量子几乎均匀地分布在两个光系统中。通过分析光2对远红光下测量的能量储存的增强现象得出了这一结论。光1对光2下测量的能量储存的降低作用也与此结论一致。光声实验表明,光1中有显著的能量储存,这可以用光系统I周围的循环电子传递来解释。通过对背景光2增强效应(最大增强为1.4 - 1.5)的定量分析表明,约70%的光1分布到这种光系统I的循环传递中。