Suppr超能文献

光合作用。氧释放复合体在 O-O 键形成之前的电子结构在光系统 II 中。

Photosynthesis. Electronic structure of the oxygen-evolving complex in photosystem II prior to O-O bond formation.

机构信息

Max Planck Institute for Chemical Energy Conversion, Stiftstrasse 34-36, D-45470 Mülheim an der Ruhr, Germany.

Institut de Biologie et de Technologies de Saclay, CNRS UMR 8221, Commissariat à l'Énergie Atomique (CEA) Saclay, 91191 Gif-sur-Yvette, France.

出版信息

Science. 2014 Aug 15;345(6198):804-8. doi: 10.1126/science.1254910. Epub 2014 Aug 14.

Abstract

The photosynthetic protein complex photosystem II oxidizes water to molecular oxygen at an embedded tetramanganese-calcium cluster. Resolving the geometric and electronic structure of this cluster in its highest metastable catalytic state (designated S3) is a prerequisite for understanding the mechanism of O-O bond formation. Here, multifrequency, multidimensional magnetic resonance spectroscopy reveals that all four manganese ions of the catalyst are structurally and electronically similar immediately before the final oxygen evolution step; they all exhibit a 4+ formal oxidation state and octahedral local geometry. Only one structural model derived from quantum chemical modeling is consistent with all magnetic resonance data; its formation requires the binding of an additional water molecule. O-O bond formation would then proceed by the coupling of two proximal manganese-bound oxygens in the transition state of the cofactor.

摘要

光合作用蛋白复合物光系统 II 在嵌入式四锰-钙簇中将水氧化为氧气。解析该簇在其最高亚稳催化态(指定为 S3)中的几何和电子结构是理解 O-O 键形成机制的前提。在这里,多频、多维磁共振波谱揭示,在最终的氧气释放步骤之前,催化剂的所有四个锰离子在结构和电子上都是相似的;它们都表现出 4+ 的形式氧化态和八面体的局部几何形状。只有一个源自量子化学建模的结构模型与所有磁共振数据一致;其形成需要结合一个额外的水分子。然后,O-O 键的形成将通过辅因子过渡态中两个邻近锰结合氧的耦合来进行。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验