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Going around the Kok cycle of the water oxidation reaction with femtosecond X-ray crystallography
Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, CA, Berkeley, United States.
Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, CA, Berkeley, United States.
Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, CA, Berkeley, United States.
Department of Biology, Humboldt-Universität zu Berlin, Berlin, Germany.
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2023 (English)In: IUCrJ, E-ISSN 2052-2525, Vol. 10, no 6, p. 642-655Article, review/survey (Refereed) Published
Abstract [en]

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.

Place, publisher, year, edition, pages
International Union Of Crystallography, 2023. Vol. 10, no 6, p. 642-655
Keywords [en]
manganese metalloenzymes, oxygen evolving complex, photosystem II, water-splitting, wateroxidation, X-ray free-electron lasers, X-ray spectroscopy
National Category
Structural Biology Organic Chemistry
Identifiers
URN: urn:nbn:se:umu:diva-217019DOI: 10.1107/S2052252523008928ISI: 001098137800003Scopus ID: 2-s2.0-85176617926OAI: oai:DiVA.org:umu-217019DiVA, id: diva2:1814467
Conference
The IUCr 2023 Congress, 22-29 August 2023, Melbourne, Australia,
Available from: 2023-11-24 Created: 2023-11-24 Last updated: 2025-04-24Bibliographically approved

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Messinger, Johannes

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