Dependence of the rate-limiting steps in the dark-to-light transition of photosystem II on the lipidic environment of the reaction center.

In our earlier works, we have identified rate-limiting steps in the dark-to-light transition of PSII. By measuring chlorophyll fluorescence transients elicited by single-turnover saturating flashes (STSFs) we have shown that in diuron-treated samples an STSF generates only F (< F) fluorescence level, and to produce the maximum (F) level, additional excitations are required, which, however, can only be effective if sufficiently long Δ waiting times are allowed between the excitations. Biological variations in the half-rise time (Δ ) of the fluorescence increment suggest that it may be sensitive to the physicochemical environment of PSII. Here, we investigated the influence of the lipidic environment on Δ of PSII core complexes of . We found that while non-native lipids had no noticeable effects, thylakoid membrane lipids considerably shortened the Δ , from ~ 1 ms to ~ 0.2 ms. The importance of the presence of native lipids was confirmed by obtaining similarly short Δ values in the whole cells and isolated pea thylakoid membranes. Minor, lipid-dependent reorganizations were also observed by steady-state and time-resolved spectroscopic measurements. These data show that the processes beyond the dark-to-light transition of PSII depend significantly on the lipid matrix of the reaction center.