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本文引用的文献

1
Subunit and chlorophyll organization of the plant photosystem II supercomplex.植物光系统 II 超复合体的亚基和叶绿素组织。
Nat Plants. 2017 Jun 12;3:17080. doi: 10.1038/nplants.2017.80.
2
'Photosystem II: the water splitting enzyme of photosynthesis and the origin of oxygen in our atmosphere'.光系统II:光合作用中的水裂解酶与地球大气中氧气的起源
Q Rev Biophys. 2016 Jan;49:e14. doi: 10.1017/S0033583516000093. Epub 2016 Aug 1.
3
Association of Psb28 and Psb27 Proteins with PSII-PSI Supercomplexes upon Exposure of Synechocystis sp. PCC 6803 to High Light.高光胁迫下集胞藻 PCC 6803 中 Psb28 和 Psb27 蛋白与 PSII-PSI 超复合物的关联。
Mol Plant. 2017 Jan 9;10(1):62-72. doi: 10.1016/j.molp.2016.08.001. Epub 2016 Aug 12.
4
Mutation of Gly195 of the ChlH Subunit of Mg-chelatase Reduces Chlorophyll and Further Disrupts PS II Assembly in a Ycf48-Deficient Strain of Synechocystis sp. PCC 6803.集胞藻PCC 6803中Ycf48缺陷菌株里镁螯合酶ChlH亚基的Gly195突变会减少叶绿素含量并进一步破坏PS II组装
Front Plant Sci. 2016 Jul 20;7:1060. doi: 10.3389/fpls.2016.01060. eCollection 2016.
5
CyanoP is Involved in the Early Steps of Photosystem II Assembly in the Cyanobacterium Synechocystis sp. PCC 6803.氰基蛋白参与集胞藻6803中光系统II组装的早期步骤。
Plant Cell Physiol. 2016 Sep;57(9):1921-31. doi: 10.1093/pcp/pcw115. Epub 2016 Jul 7.
6
Structure of spinach photosystem II-LHCII supercomplex at 3.2 Å resolution.菠菜光系统 II-LHCII 超级复合物的 3.2Å 分辨率结构。
Nature. 2016 Jun 2;534(7605):69-74. doi: 10.1038/nature18020. Epub 2016 May 18.
7
Photoactivation: The Light-Driven Assembly of the Water Oxidation Complex of Photosystem II.光激活:光系统II水氧化复合物的光驱动组装
Front Plant Sci. 2016 May 3;7:578. doi: 10.3389/fpls.2016.00578. eCollection 2016.
8
ConSurf 2016: an improved methodology to estimate and visualize evolutionary conservation in macromolecules.ConSurf 2016:一种用于估计和可视化大分子进化保守性的改进方法。
Nucleic Acids Res. 2016 Jul 8;44(W1):W344-50. doi: 10.1093/nar/gkw408. Epub 2016 May 10.
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Analysis of photosystem II biogenesis in cyanobacteria.蓝细菌中光系统II生物合成的分析。
Biochim Biophys Acta. 2016 Mar;1857(3):274-87. doi: 10.1016/j.bbabio.2015.11.007. Epub 2015 Dec 1.
10
The Structure of Photosystem II and the Mechanism of Water Oxidation in Photosynthesis.光合作用中光系统 II 的结构和水氧化的机制。
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Ycf48 参与了放氧光合作用光系统 II 复合物的生物发生,是一种七叶β-螺旋桨蛋白。

Ycf48 involved in the biogenesis of the oxygen-evolving photosystem II complex is a seven-bladed beta-propeller protein.

机构信息

Wolfson Laboratories, Department of Life Sciences, Imperial College London, SW7 2AZ London, United Kingdom;

Centre Algatech, Institute of Microbiology, Czech Academy of Sciences, 37981 Třeboň, Czech Republic.

出版信息

Proc Natl Acad Sci U S A. 2018 Aug 14;115(33):E7824-E7833. doi: 10.1073/pnas.1800609115. Epub 2018 Jul 30.

DOI:10.1073/pnas.1800609115
PMID:30061392
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6099905/
Abstract

Robust photosynthesis in chloroplasts and cyanobacteria requires the participation of accessory proteins to facilitate the assembly and maintenance of the photosynthetic apparatus located within the thylakoid membranes. The highly conserved Ycf48 protein acts early in the biogenesis of the oxygen-evolving photosystem II (PSII) complex by binding to newly synthesized precursor D1 subunit and by promoting efficient association with the D2 protein to form a PSII reaction center (PSII RC) assembly intermediate. Ycf48 is also required for efficient replacement of damaged D1 during the repair of PSII. However, the structural features underpinning Ycf48 function remain unclear. Here we show that Ycf48 proteins encoded by the thermophilic cyanobacterium and the red alga form seven-bladed beta-propellers with the 19-aa insertion characteristic of eukaryotic Ycf48 located at the junction of blades 3 and 4. Knowledge of these structures has allowed us to identify a conserved "Arg patch" on the surface of Ycf48 that is important for binding of Ycf48 to PSII RCs but also to larger complexes, including trimeric photosystem I (PSI). Reduced accumulation of chlorophyll in the absence of Ycf48 and the association of Ycf48 with PSI provide evidence of a more wide-ranging role for Ycf48 in the biogenesis of the photosynthetic apparatus than previously thought. Copurification of Ycf48 with the cyanobacterial YidC protein insertase supports the involvement of Ycf48 during the cotranslational insertion of chlorophyll-binding apopolypeptides into the membrane.

摘要

叶绿体和蓝藻中的光合作用需要辅助蛋白的参与,以促进位于类囊体膜内的光合作用装置的组装和维持。高度保守的 Ycf48 蛋白通过与新合成的前体 D1 亚基结合,并促进与 D2 蛋白的有效结合,形成 PSII 反应中心(PSII RC)组装中间体,从而在氧产生光系统 II(PSII)复合物的生物发生早期发挥作用。Ycf48 对于 PSII 修复过程中受损 D1 的有效替换也是必需的。然而,支撑 Ycf48 功能的结构特征尚不清楚。在这里,我们展示了嗜热蓝藻 和红藻编码的 Ycf48 蛋白形成具有 19 个氨基酸插入特征的七叶β-螺旋桨,该插入特征存在于真核 Ycf48 的叶 3 和叶 4 的交界处。这些结构的知识使我们能够识别 Ycf48 表面上保守的“Arg 补丁”,该补丁对于 Ycf48 与 PSII RC 的结合很重要,但对于更大的复合物,包括三聚体光系统 I(PSI)也是如此。在没有 Ycf48 的情况下叶绿素的积累减少,以及 Ycf48 与 PSI 的关联,为 Ycf48 在光合作用装置的生物发生中比以前认为的更广泛的作用提供了证据。Ycf48 与蓝藻 YidC 蛋白插入酶的共纯化支持了 Ycf48 在叶绿体外多肽的共翻译插入到膜中的参与。