Oxygen evolution by photosystem II (PSII) is activated by chloride and other monovalent anions. In this study, the effects of iodide on oxygen evolution activity were investigated using PSII-enriched membrane fragments from spinach. In the absence of Cl-, the dependence of oxygen evolution activity on I- concentration showed activation followed by inhibition in both intact PSII and NaCl-washed PSII, which lacked the PsbP and PsbQ subunits. Using a substrate inhibition model, the range of values of the Michaelis constant KM in intact PSII (0.5-1.5 mM) was smaller than that in NaCl-washed PSII (1.5-5 mM), whereas values of the inhibition constant K-I in intact PSII (9-17 mM) were larger than those in NaCl-washed PSII (1-4 mM). Studies of I- inhibition of Cl--activated oxygen evolution in intact PSII revealed that I- was primarily an uncompetitive inhibitor, with uncompetitive constant K-i' = 37 mM and Cl--competitive constant Ki > 200 mM. This result indicated that the activating Cl- must be bound for inhibition to take place, which is consistent with the substrate inhibition model for I- activation. The S-2 state multiline and g = 4.1 EPR signals in NaCl-washed PSII were examined in the presence of 3 and 25 mM NaI, corresponding to I--activated and I--inhibited conditions, respectively. The two S2 state signals were observed at both I- concentrations, indicating that I- substitutes for Cl- in formation of the signals and that advancement to the S-2 state was not prevented by high I- concentrations. A model is presented that incorporates the results of this study, including the action of both chloride and iodide.