One prominent difference between the photosystem II (PSII) reaction center
protein D1 ' in Synechocystis 6803 and normal D1 is the replacement of Phe-
186 in D1 with leucine in D1 '. Mutants of Synechocystis 6803 producing onl
y D1 ', or containing engineered D1 proteins with Phe-186 substitutions, we
re analyzed by 77 K fluorescence emission spectra, chlorophyll a fluorescen
ce induction yield and decay kinetics, and flash-induced oxygen evolution.
Compared to D1-containing PSII centers, D1 ' centers exhibited a 50% reduct
ion in variable chlorophyll a fluorescence yield, while the flash-induced O
-2 evolution pattern was unaffected. In the F186 mutants, both the P680(+)/
Q(A)(-) recombination and O-2 oscillation pattern were noticeably perturbed
. (C) 2001 Published by Elsevier Science B.V. on behalf of the Federation o
f European Biochemical Societies.