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Low-temperature electron transfer suggests two types of QA in intact photosystem II
Authors:Han Bao  Yanan Ren  Jingquan Zhao
Institution:Laboratory of Photochemistry, Beijing National Laboratory of Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China
Abstract:The correlation between the reduction of QA and the oxidation of TyrZ or Car/ChlZ/Cytb559 in spinach PSII enriched membranes induced by visible light at 10 K is studied by using electron paramagnetic resonance spectroscopy. Similar g = 1.95-1.86 QA-•EPR signals are observed in both Mn-depleted and intact samples, and both signals are long lived at low temperatures. The presence of PPBQ significantly diminished the light induced EPR signals from QA-•, Car+•/Chl+• and oxidized Cytb559, while enhancing the amplitude of the S1TyrZ• EPR signal in the intact PSII sample. The quantification and stability of the g = 1.95-1.86 EPR signal and signals arising from the oxidized TyrZ and the side-path electron donors, respectively, indicate that the EPR-detectable g = 1.95-1.86 QA-• signal is only correlated to reaction centers undergoing oxidation of the side-path electron donors (Car/ChlZ/Cytb559), but not of TyrZ. These results imply that two types of QA-• probably exist in the intact PSII sample. The structural difference and possible function of the two types of QA are discussed.
Keywords:Chl  chlorophyll  ChlZ  side-path redox active Chl  Car  redox active β-carotene  Cytb559  cytochrome b559  D1  D2  reaction center core proteins  DMSO  dimethyl sulfoxide  EDTA  ethylenediaminetetraacetic acid  EPR  electron paramagnetic resonance  MES  4-morpholine ethanesulfonic acid  P680  primary electron donor of PSII  PD1  PD2  two monomeric Chls of P680 associated with D1 and D2  respectively  Pheo  pheophytin  PPBQ  phenyl-p-benzoquinone  PSII  photosystem II  PQ  plastoquinone  PQH2  plastoquinol  QA and QB  primary and secondary quinone electron acceptors  respectively  TyrD  tyrosine 161 of the D1 protein  TyrZ  tyrosine 160 of the D2 protein
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