The oxygen-evolving complex (OEC), also known as the water-splitting complex, is a water-oxidizing enzyme involved in the photo-oxidation of water during the light reactions of photosynthesis.[3] OEC is surrounded by 4 core proteins of photosystem II at the membrane-lumen interface. The mechanism for splitting water involves absorption of three photons before the fourth provides sufficient energy for water oxidation.[4] Based on a widely accepted theory from 1970 by Kok, the complex can exist in 5 states, denoted S0 to S4, with S0 the most reduced and S4 the most oxidized. Photons trapped by photosystem II move the system from state S0 to S1 to S2 to S3 and finally to S4. S4 reacts with water producing free oxygen:

2 H2O → O2 + 4 H+ + 4 e
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The Kok cycle. The oxidation state of the manganese centres is subject to debate.[1]
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X-ray crystal structure of the Mn4O5Ca core of the oxygen evolving complex of Photosystem II at a resolution of 1.9 Å.[2]

This conversion resets the catalyst to the S0 state.

The active site of the OEC consists of a cluster of manganese and calcium with the formula Mn4Ca1OxCl1–2(HCO3)y. This cluster is bound to D1 and CP43 subunits and stabilized by peripheral membrane proteins. Many characteristics of it have been examined by flash photolysis experiments, electron paramagnetic resonance (EPR), and X-ray spectroscopy.[5]

The mechanism of the complex is proposed to involve an Mn-oxide which couples by O-O bond formation to a calcium oxide/hydroxide.[6][7] [8]

References

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