Rapid Evolution of the Photosystem II Electronic Structure during Water Splitting

Abstract

Photosynthetic water oxidation is a fundamental process that sustains the biosphere. A Mn$_{4}$Ca cluster embedded in the photosystem II protein environment is responsible for the production of atmospheric oxygen. Here, time-resolved x-ray emission spectroscopy (XES) was used to observe the process of oxygen formation in real time. These experiments reveal that the oxygen evolution step, initiated by three sequential laser flashes, is accompanied by rapid (within 50 $\mu$s) changes to the Mn K$\beta$ XES spectrum. However, no oxidation of the Mn$_{4}$Ca core above the all Mn$^{\text{IV}}$ state was detected to precede O-O bond formation. A new mechanism featuring Mn$^{\text{IV}}$=O formation in the S$_{3}$ state is proposed to explain the spectroscopic results. This chemical formulation is consistent with the unique reactivity of the S$_{3}$ state and explains facilitation of the following S$_{3}$ to S$_{0}$ transition, resolving in part the kinetic limitations associated with O-O bond formation. In the proposed mechanism, O-O bond formation precedes transfer of the final (4$^{\text{th}}$) electron from the Mn$_{4}$Ca cluster, in agreement with experiment.