The First State in the Catalytic Cycle of the Water-Oxidizing Enzyme: Identification of a Water-Derived μ-Hydroxo Bridge
2017
Lohmiller, Thomas | Krewald, Vera | Sedoud, Arezki | Rutherford, A William | Neese, Frank | Lubitz, Wolfgang | Pantazis, Dimitrios A. | Cox, Nicholas
Nature’s water-splitting catalyst, an oxygen-bridged tetramanganese calcium (Mn₄O₅Ca) complex, sequentially activates two substrate water molecules generating molecular O₂. Its reaction cycle is composed of five intermediate (Sᵢ) states, where the index i indicates the number of oxidizing equivalents stored by the cofactor. After formation of the S₄ state, the product dioxygen is released and the cofactor returns to its lowest oxidation state, S₀. Membrane-inlet mass spectrometry measurements suggest that at least one substrate is bound throughout the catalytic cycle, as the rate of ¹⁸O-labeled water incorporation into the product O₂ is slow, on a millisecond to second time scale depending on the S state. Here, we demonstrate that the Mn₄O₅Ca complex poised in the S₀ state contains an exchangeable hydroxo bridge. On the basis of a combination of magnetic multiresonance (EPR) spectroscopies, comparison to biochemical models and theoretical calculations we assign this bridge to O5, the same bridge identified in the S₂ state as an exchangeable fully deprotonated oxo bridge [Pérez Navarro, M.; et al. Proc. Natl. Acad. Sci. U.S.A. 2013, 110, 15561]. This oxygen species is the most probable candidate for the slowly exchanging substrate water in the S₀ state. Additional measurements provide new information on the Mn ions that constitute the catalyst. A structural model for the S₀ state is proposed that is consistent with available experimental data and explains the observed evolution of water exchange kinetics in the first three states of the catalytic cycle.
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