Molecular basis for turnover inefficiencies (misses) during water oxidation in photosystem IIVisa övriga samt affilieringar
2022 (Engelska)Ingår i: Chemical Science, ISSN 2041-6520, E-ISSN 2041-6539, Vol. 13, nr 29, s. 8667-8678Artikel i tidskrift (Refereegranskat) Published
Abstract [en]
Photosynthesis stores solar light as chemical energy and efficiency of this process is highly important. The electrons required for CO2 reduction are extracted from water in a reaction driven by light-induced charge separations in the Photosystem II reaction center and catalyzed by the CaMn4O5-cluster. This cyclic process involves five redox intermediates known as the S0-S4 states. In this study, we quantify the flash-induced turnover efficiency of each S state by electron paramagnetic resonance spectroscopy. Measurements were performed in photosystem II membrane preparations from spinach in the presence of an exogenous electron acceptor at selected temperatures between −10 °C and +20 °C and at flash frequencies of 1.25, 5 and 10 Hz. The results show that at optimal conditions the turnover efficiencies are limited by reactions occurring in the water oxidizing complex, allowing the extraction of their S state dependence and correlating low efficiencies to structural changes and chemical events during the reaction cycle. At temperatures 10 °C and below, the highest efficiency (i.e. lowest miss parameter) was found for the S1 → S2 transition, while the S2 → S3 transition was least efficient (highest miss parameter) over the whole temperature range. These electron paramagnetic resonance results were confirmed by measurements of flash-induced oxygen release patterns in thylakoid membranes and are explained on the basis of S state dependent structural changes at the CaMn4O5-cluster that were determined recently by femtosecond X-ray crystallography. Thereby, possible "molecular errors" connected to the e− transfer, H+ transfer, H2O binding and O2 release are identified.
Ort, förlag, år, upplaga, sidor
Royal Society of Chemistry, 2022. Vol. 13, nr 29, s. 8667-8678
Nationell ämneskategori
Biofysik Fysikalisk kemi
Identifikatorer
URN: urn:nbn:se:umu:diva-199017DOI: 10.1039/d2sc00854hISI: 000823810200001PubMedID: 35974765Scopus ID: 2-s2.0-85136262938OAI: oai:DiVA.org:umu-199017DiVA, id: diva2:1692513
Forskningsfinansiär
Vetenskapsrådet, 2020-03809NordForsk, 828452022-09-022022-09-022025-02-20Bibliografiskt granskad