Contributions of PD1 and PD2 to the [PD1PD2]+-minus-[PD1PD2] difference spectrum in the Soret region in Photosystem II

Flash-induced absorption changes in the Soret region, which originate from the [PD1PD2]+ state, the chlorophyll cation radical formed upon Photosystem II (PSII) excitation, were investigated in Mn-depleted Photosystem II. In wild-type PSII from Thermosynechococcus elongatus , the [PD1PD2]+- minus -[PD1PD2] difference spectrum shows a main negative feature at 434 nm and a smaller negative feature at 446 nm [Boussac et al. Photosynth Res (2023), ]. While the main feature at 434 nm is associated with PD1+ formation, the origin of the dip at 446 nm remains to be identified. For that, we have compared the [PD1PD2]+- minus -[PD1PD2] difference spectra from the PsbA3/H198Q PSII mutant in T. elongatus and D2/H197A PSII mutant in Synechocystis sp. PCC 6803 with their respective wild type strains. By modifying the PD1 axial ligand with the H198Q mutation in the D1 protein in T. elongatus , the contribution at 434 nm was shifted to 431 nm, while the contribution at 446 nm was hardly affected. In Synechocystis sp. PCC 6803, by modifying the PD2 axial ligand with the H197A mutation in the D2 protein, the contribution at 446 nm was downshifted by ∼ 3 nm to ∼ 443 nm, while the main contribution at 432 nm was only slightly shifted upwards to 433 nm. This result suggests that the bleaching seen at 446 nm involves PD2. This could reflects a change in the [PD1+PD2]⟷[PD1PD2+] equilibrium or a more complex mechanism. ### Competing Interest Statement The authors have declared no competing interest. * Chl : chlorophyll ChlD1/ChlD2 : monomeric Chl on the D1 or D2 side, respectively PD1 and PD2 : individual Chl on the D1 or D2 side, respectively, which constitute a pair of Chl with partially overlapping aromatic rings (P680) PheD1 and PheD2 : pheophytin on the D1 or D2 side, respectively PPBQ : phenyl p –benzoquinone PSII : Photosystem II QA : primary quinone acceptor QB : secondary quinone acceptor TyrD : the tyrosine 160 of D2 acting as a side-path electron donor of PSII TyrZ : the tyrosine 161 of D1 acting as the electron donor to P680