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连续缺失光系统 II 组装因子 Ycf48、Ycf39 和 Pam68 导致蓝藻集胞藻 PCC 6803 的自主光合作用逐渐丧失。

Sequential deletions of photosystem II assembly factors Ycf48, Ycf39 and Pam68 result in progressive loss of autotrophy in the cyanobacterium Synechocystis PCC 6803.

机构信息

Centre Algatech, Institute of Microbiology, Czech Academy of Sciences, 379 81, Třeboň, Czech Republic.

出版信息

Folia Microbiol (Praha). 2019 Sep;64(5):683-689. doi: 10.1007/s12223-019-00736-w. Epub 2019 Jul 29.

Abstract

The biogenesis of the cyanobacterial photosystem II (PSII) complex requires a number of auxiliary assembly factors that improve efficiency of the process but their precise function is not well understood. To assess a possible synergic action of the Ycf48 and Ycf39 factors acting in early steps of the biogenesis via interaction with the nascent D1 subunit of PSII, we constructed and characterised a double mutant of the cyanobacterium Synechocystis PCC 6803 lacking both these proteins. In addition, we also deleted the ycf39 gene in the double mutant lacking Ycf48 and Pam68, the latter being a ribosomal factor promoting insertion of chlorophyll (Chl) into the CP47 subunit of PSII. The resulting double ΔYcf48/ΔYcf39 and triple ΔYcf48/ΔPam68/ΔYcf39 mutants were deficient in PSII and total Chl, and in contrast to the source mutants, they lost the capacity for autotrophy. Interestingly, autotrophic growth was restored in both of the new multiple mutants by enhancing Chl biosynthesis using a specific ferrochelatase inhibitor. Taking together with the weak radioactive labelling of the D1 protein, these findings can be explained by inhibition of the D1 synthesis caused by the lack and/or incorrect binding of Chl molecules. The results emphasise the key importance of the sufficient Chl supply for the PSII biogenesis and also support the existence of a so far enigmatic regulatory mechanism leading to the reduced overall Chl biosynthesis/accumulation when the PSII assembly is impaired.

摘要

蓝藻光合系统 II(PSII)复合物的生物发生需要多种辅助组装因子,这些因子可以提高该过程的效率,但它们的确切功能尚不清楚。为了评估在生物发生的早期步骤中通过与 PSII 新生 D1 亚基相互作用而作用的 Ycf48 和 Ycf39 因子的协同作用,我们构建并表征了一种缺乏这两种蛋白质的集胞藻 PCC 6803 的双突变体。此外,我们还在缺乏 Ycf48 和 Pam68 的双突变体中缺失了 ycf39 基因,Pam68 是一种促进 Chl(叶绿素)插入 PSII 的 CP47 亚基的核糖体因子。由此产生的双ΔYcf48/ΔYcf39 和三ΔYcf48/ΔPam68/ΔYcf39 突变体缺乏 PSII 和总 Chl,与原始突变体不同,它们失去了自养能力。有趣的是,通过使用特定的亚铁螯合酶抑制剂增强 Chl 生物合成,两种新的多突变体都恢复了自养生长。与放射性标记 D1 蛋白的弱标记相结合,这些发现可以通过缺乏和/或 Chl 分子的不正确结合引起的 D1 合成的抑制来解释。这些结果强调了充足的 Chl 供应对 PSII 生物发生的关键重要性,并且还支持存在一种迄今为止神秘的调节机制,当 PSII 组装受损时,该机制会导致整体 Chl 生物合成/积累减少。

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