| Literature DB >> 25124437 |
Nicholas Cox1, Marius Retegan2, Frank Neese2, Dimitrios A Pantazis2, Alain Boussac3, Wolfgang Lubitz1.
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.Entities:
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Year: 2014 PMID: 25124437 DOI: 10.1126/science.1254910
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728