Early Binding of Substrate Oxygen Is Responsible for a Spectroscopically Distinct S₂ State in Photosystem II

The biological generation of oxygen by the oxygen-evolving complex (OEC) in photosystem II (PS II) is one of nature’s most important reactions. The OEC is a Mn 4 Ca cluster that has multiple Mn–O–Mn and Mn–O–Ca bridges and binds four water molecules. Previously, binding of an additional oxygen was detected in the S 2 to S 3 transition. Here we demonstrate that early binding of the substrate oxygen to the five-coordinate Mn 1 center in the S 2 state is likely responsible for the S 2 high-spin EPR signal. Substrate binding in the Mn 1 –OH form explains the prevalence of the high-spin S 2 state at higher pH and its low-temperature conversion into the S 3 state. The given interpretation was confirmed by X-ray absorption spectroscopic measurements, DFT, and broken symmetry DFT calculations of structures and magnetic properties. Structural, electronic, and spectroscopic properties of the high-spin S 2 state model are provided and compared with the available S 3 state models. New interpretation of the high-spin S 2 state opens opportunity for analysis of factors controlling the oxygen substrate binding in PS II.