Klinkert Birgit, Ossenbühl Friedrich, Sikorski Martha, Berry Stefan, Eichacker Lutz, Nickelsen Jörg
Allgemeine und Molekulare Botanik, Ruhr-Universität Bochum, Germany.
J Biol Chem. 2004 Oct 22;279(43):44639-44. doi: 10.1074/jbc.M405393200. Epub 2004 Aug 24.
The light reactions of oxygenic photosynthesis are mediated by multisubunit pigment-protein complexes situated within the specialized thylakoid membrane system. The biogenesis of these complexes is regulated by transacting factors that affect the expression of the respective subunit genes and/or the assembly of their products. Here we report on the analysis of the PratA gene from the cyanobacterium Synechocystis sp. PCC 6803 that encodes a periplasmic tetratricopeptide repeat protein of formerly unknown function. Targeted inactivation of PratA resulted in drastically reduced photosystem II (PSII) content. Protein pulse labeling experiments of PSII subunits indicated that the C-terminal processing of the precursor of the reaction center protein D1 is compromised in the pratA mutant. Moreover, a direct interaction of PratA and precursor D1 was demonstrated by applying yeast two-hybrid analyses. This suggests that PratA represents a factor facilitating D1 maturation via the endoprotease CtpA. The periplasmic localization of PratA supports a model that predicts the initial steps of PSII biogenesis to occur at the plasma membrane of cyanobacterial cells.
产氧光合作用的光反应由位于特殊类囊体膜系统内的多亚基色素蛋白复合物介导。这些复合物的生物合成受反式作用因子调控,这些因子影响各自亚基基因的表达和/或其产物的组装。在此,我们报告对来自集胞藻属PCC 6803蓝细菌的PratA基因的分析,该基因编码一种功能未知的周质四肽重复蛋白。PratA的靶向失活导致光系统II(PSII)含量大幅降低。PSII亚基的蛋白质脉冲标记实验表明,反应中心蛋白D1前体的C端加工在pratA突变体中受到损害。此外,通过酵母双杂交分析证明了PratA与前体D1之间存在直接相互作用。这表明PratA代表一种通过内肽酶CtpA促进D1成熟的因子。PratA的周质定位支持了一个预测PSII生物合成初始步骤发生在蓝细菌细胞质膜上的模型。