Malkin S, Armond P A, Mooney H A, Fork D C
Department of Plant Biology, Carnegie Institution of Washington, Stanford University, Stanford, California 94305.
Plant Physiol. 1981 Mar;67(3):570-9. doi: 10.1104/pp.67.3.570.
The use of fluorescence induction measurements in leaves infiltrated with 3-(3,4-dichlorophenyl)-1,1-dimethylurea has been evaluated as a routine method for estimation of the concentration of the reaction centers of photosystem II relative to total chlorophyll in a wide variety of plant species. The procedure is based on a simple theory that takes into account the attenuation of light in passing through the leaf and the linear dependence of the fluorescence induction time from different parts of the leaf on the inverse of the local light intensity. A formula to calculate the reaction center concentration of photosystem II was obtained. The effect of the light attenuation is accounted for by a correction factor which could become practically insignificant by an optimal choice of the excitation and emission wavelengths and the geometry of the photodetector with respect to the sample. Estimation of quantum yields for primary photochemistry and influence of light scattering were considered. The results demonstrate the effect of the above factors under various circumstances and are in agreement, to a first approximation, with the theory.THE UTILITY OF THE METHOD IS DEMONSTRATED BY A DETAILED STUDY OF FOUR DESERT PLANT SPECIES: estimation of reaction center concentrations of both photosystem I (by estimation of P700) and photosystem II (by the fluorescence induction method) were made and were compared to the rates of CO(2) fixation. There was a good quantitative correlation between the photosynthetic rates and the concentration of photosystem II reaction centers (expressed as per chlorophyll or per unit area of the leaf), but no such correlation was found with photosystem I reaction centers.The ratio of total chlorophyll per reaction centers II varied in the range of about 200 to 800 in different species, but there was no variation of this parameter in any single species.
用3-(3,4-二氯苯基)-1,1-二甲基脲浸润叶片后进行荧光诱导测量,已被评估为一种常规方法,用于估算多种植物物种中光系统II反应中心浓度相对于总叶绿素的浓度。该程序基于一个简单的理论,该理论考虑了光穿过叶片时的衰减以及叶片不同部位的荧光诱导时间与局部光强倒数的线性关系。得到了一个计算光系统II反应中心浓度的公式。光衰减的影响由一个校正因子来考虑,通过对激发和发射波长以及光探测器相对于样品的几何形状进行优化选择,该校正因子实际上可能变得微不足道。考虑了初级光化学量子产率的估算以及光散射的影响。结果表明了上述因素在各种情况下的作用,并且在一阶近似下与理论相符。通过对四种沙漠植物物种的详细研究证明了该方法的实用性:对光系统I(通过估算P700)和光系统II(通过荧光诱导法)的反应中心浓度进行了估算,并与CO₂固定速率进行了比较。光合速率与光系统II反应中心浓度(以每叶绿素或每单位叶面积表示)之间存在良好的定量相关性,但与光系统I反应中心没有这种相关性。不同物种中每个反应中心II的总叶绿素比率在约200至800的范围内变化,但在任何单个物种中该参数没有变化。