Shimazaki K, Zeiger E
Department of Biological Sciences, Stanford University, Stanford, California 94305.
Plant Physiol. 1985 Jun;78(2):211-4. doi: 10.1104/pp.78.2.211.
High rates of both cyclic and noncyclic photophosphorylation were measured in chloroplast lamellae isolated from purified guard cell protoplasts from Vicia faba L. Typical rates of light-dependent incorporation of (32)P into ATP were 100 and 190 micromoles ATP per milligram chlorophyll per hour for noncyclic (water to ferricyanide) and cyclic (phenazine methosulfate) photophosphorylation, respectively. These rates were 50 to 80% of those observed with mesophyll chloroplasts. Noncyclic photophosphorylation in guard cell chloroplasts was completely inhibited by 3-(3,4-dichlorophenyl)-1,1-dimethylurea supporting the notion that photophosphorylation is coupled to linear electron flow from photosystem II to photosystem I. Several lines of evidence indicated that contamination by mesophyll chloroplasts cannot account for the observed photophosphorylation rates.A comparison of the photon fluence dependence of noncyclic photophosphorylation in mesophyll and guard cell chloroplasts showed significant differences between the two preparations, with half saturation at 0.04 and 0.08 millimole per square meter per second, respectively.
从蚕豆纯化保卫细胞原生质体分离得到的叶绿体片层中,检测到了较高的循环和非循环光合磷酸化速率。非循环(水到铁氰化物)和循环(吩嗪硫酸甲酯)光合磷酸化过程中,光依赖的(32)P掺入ATP的典型速率分别为每毫克叶绿素每小时100和190微摩尔ATP。这些速率是叶肉叶绿体中观察到的速率的50%至80%。保卫细胞叶绿体中的非循环光合磷酸化被3-(3,4-二氯苯基)-1,1-二甲基脲完全抑制,这支持了光合磷酸化与从光系统II到光系统I的线性电子流偶联的观点。几条证据表明,叶肉叶绿体的污染不能解释观察到的光合磷酸化速率。叶肉和保卫细胞叶绿体中非循环光合磷酸化的光子通量依赖性比较显示,两种制剂之间存在显著差异,半饱和状态分别为每秒每平方米0.04和0.08毫摩尔。