Barbato R, Friso G, Rigoni F, Dalla Vecchia F, Giacometti G M
Dipartimento di Biologia, Universita di Padova, Italy.
J Cell Biol. 1992 Oct;119(2):325-35. doi: 10.1083/jcb.119.2.325.
The structural and topological stability of thylakoid components under photoinhibitory conditions (4,500 microE.m-2.s-1 white light) was studied on Mn depleted thylakoids isolated from spinach leaves. After various exposures to photoinhibitory light, the chlorophyll-protein complexes of both photosystems I and II were separated by sucrose gradient centrifugation and analysed by Western blotting, using a set of polyclonals raised against various apoproteins of the photosynthetic apparatus. A series of events occurring during donor side photoinhibition are described for photosystem II, including: (a) lowering of the oligomerization state of the photosystem II core; (b) cleavage of 32-kD protein D1 at specific sites; (c) dissociation of chlorophyll-protein CP43 from the photosystem II core; and (d) migration of damaged photosystem II components from the grana to the stroma lamellae. A tentative scheme for the succession of these events is illustrated. Some effects of photoinhibition on photosystem I are also reported involving dissociation of antenna chlorophyll-proteins LHCI from the photosystem I reaction center.
在从菠菜叶片中分离出的缺锰类囊体上,研究了光抑制条件(4500微爱因斯坦·米⁻²·秒⁻¹白光)下类囊体成分的结构和拓扑稳定性。在各种光抑制光照处理后,通过蔗糖梯度离心分离光系统I和II的叶绿素-蛋白复合物,并使用针对光合机构各种脱辅基蛋白产生的一组多克隆抗体进行蛋白质免疫印迹分析。描述了光系统II供体侧光抑制过程中发生的一系列事件,包括:(a)光系统II核心寡聚化状态降低;(b)32-kD蛋白D1在特定位点的切割;(c)叶绿素-蛋白CP43从光系统II核心解离;(d)受损的光系统II成分从基粒迁移到基质类囊体。展示了这些事件相继发生的初步示意图。还报道了光抑制对光系统I的一些影响,包括天线叶绿素-蛋白LHCI从光系统I反应中心的解离。