Abstract

The O2-producing Mn4CaO5 catalyst in photosystem II oxidizes two water molecules (substrate) to produce one O2 molecule. Considerable evidence supports the identification of one of the two substrate waters as the Mn4CaO5 cluster's oxo bridge known as O5. The identity of the second substrate water molecule is less clear. In one set of models, the second substrate is the Mn-bound water molecule known as W2. In another set of models, the second substrate is the Ca2+-bound water molecule known as W3. In all of these models, a deprotonated form of the second substrate moves to a position next to O5 during the catalytic step immediately prior to O-O bond formation. In this study, FTIR difference spectroscopy was employed to identify the vibrational modes of hydrogen-bonded water molecules that are altered by the substitution of Sr2+ for Ca2+. Our data show that the substitution substantially altered the vibrational modes of only a single water molecule: the water molecule whose D-O-D bending mode is eliminated during the catalytic step immediately prior to O-O bond formation. These data are most consistent with the identification of the Ca2+-bound W3 as the second substrate involved in O-O bond formation.

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