Going around the Kok cycle of the water oxidation reaction with femtosecond X-ray crystallography
| Autor: | Asmit Bhowmick, Philipp S. Simon, Isabel Bogacz, Rana Hussein, Miao Zhang, Hiroki Makita, Mohamed Ibrahim, Ruchira Chatterjee, Margaret D. Doyle, Mun Hon Cheah, Petko Chernev, Franklin D. Fuller, Thomas Fransson, Roberto Alonso-Mori, Aaron S. Brewster, Nicolas K. Sauter, Uwe Bergmann, Holger Dobbek, Athina Zouni, Johannes Messinger, Jan Kern, Vittal K. Yachandra, Junko Yano |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2023 |
| Předmět: | |
| Zdroj: | IUCrJ, Vol 10, Iss 6, Pp 642-655 (2023) |
| Druh dokumentu: | article |
| ISSN: | 2052-2525 20522525 |
| DOI: | 10.1107/S2052252523008928 |
| Popis: | The water oxidation reaction in photosystem II (PS II) produces most of the molecular oxygen in the atmosphere, which sustains life on Earth, and in this process releases four electrons and four protons that drive the downstream process of CO2 fixation in the photosynthetic apparatus. The catalytic center of PS II is an oxygen-bridged Mn4Ca complex (Mn4CaO5) which is progressively oxidized upon the absorption of light by the chlorophyll of the PS II reaction center, and the accumulation of four oxidative equivalents in the catalytic center results in the oxidation of two waters to dioxygen in the last step. The recent emergence of X-ray free-electron lasers (XFELs) with intense femtosecond X-ray pulses has opened up opportunities to visualize this reaction in PS II as it proceeds through the catalytic cycle. In this review, we summarize our recent studies of the catalytic reaction in PS II by following the structural changes along the reaction pathway via room-temperature X-ray crystallography using XFELs. The evolution of the electron density changes at the Mn complex reveals notable structural changes, including the insertion of OX from a new water molecule, which disappears on completion of the reaction, implicating it in the O—O bond formation reaction. We were also able to follow the structural dynamics of the protein coordinating with the catalytic complex and of channels within the protein that are important for substrate and product transport, revealing well orchestrated conformational changes in response to the electronic changes at the Mn4Ca cluster. |
| Databáze: | Directory of Open Access Journals |
| Externí odkaz: |
|