Dynamics of Proton Transfer to Internal Water during
the Photosynthetic Oxygen-Evolving Cycle
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Abstract
In
photosynthesis, the light-driven oxidation of water is a sustainable
process, which converts solar to chemical energy and produces protons
and oxygen. To enable biomimetic strategies, the mechanism of photosynthetic
oxygen evolution must be elucidated. Here, we provide information
concerning a critical step in the oxygen-evolving, or S-state, cycle.
During this S<sub>3</sub>-to-S<sub>0</sub> transition, oxygen is produced,
and substrate water binds to the manganese–calcium catalytic
site. Our spectroscopic and H<sub>2</sub><sup>18</sup>O labeling experiments
show that this S<sub>3</sub>-to-S<sub>0</sub> step is associated with
the protonation of an internal water cluster in a hydrogen-bonding
network, which contains calcium. When compared to the protonated water
cluster, formed during a preceding step, the S<sub>1</sub>-to-S<sub>2</sub> transition, the S<sub>3</sub>-to-S<sub>0</sub> hydronium
ion is likely to be coordinated by additional water molecules. This
evidence shows that internal water and the hydrogen bonding network
act as a transient proton acceptor at multiple points in the oxygen-evolving
cycle