FEBS Letters | |
Bicarbonate binding to the water‐oxidizing complex in the photosystem II. A Fourier transform infrared spectroscopy study | |
Ibarra, J.V3  Yruela, I1  Klimov, V.V2  Allakhverdiev, S.I1  | |
[1] Estación Experimental Aula Dei, Consejo Superior de Investigaciones Cientı́ficas (C.S.I.C.), Apdo. 202, 50080 Zaragoza, Spain;Institute of Soil Science and Photosynthesis, Russian Academy of Sciences, Pushchino, Moscow Region 142292, Russia;Instituto de Carboquı́mica, Consejo Superior de Investigaciones Cientı́ficas (C.S.I.C.), Poeta Luciano Gracia, 5, 50015 Zaragoza, Spain | |
关键词: Photosystem II; Bicarbonate; Donor side; Fourier transform; Infrared spectroscopy; Chl; chlorophyll; D1; polypeptide of PSII reaction center; DCBQ; 2; 6-dichlorobenzoquinone; FT-IR; Fourier transform infrared spectroscopy; MES; 2-(N-morpholino)ethanesulfonic acid; OEC; oxygen-evolving complex; Pheo; pheophytin; the primary electron acceptor; P680; the primary electron donor; PSII; photosystem II; QA and QB; primary and secondary plastoquinone electron acceptors of PSII; RC; reaction center; WOC; water-oxidizing complex; | |
DOI : 10.1016/S0014-5793(98)00271-3 | |
学科分类:生物化学/生物物理 | |
来源: John Wiley & Sons Ltd. | |
【 摘 要 】
The light-induced Fourier transform infrared difference (FT-IR) spectrum originating from the donor side of O2-evolving photosystem (PS) II was obtained in non-depleted and CO2-depleted PSII membrane preparations. The observed spectrum free of contributions from the acceptor side signals was achieved by employing 2 mM/18 mM ferri-/ferrocyanide as a redox couple. This spectrum showed main positive bands at 1589 and 1365 cm−1 and negative bands at 1560, 1541, 1522 and 1507 cm−1. CO-depleted PSII preparations showed a quite different spectrum. The main positive and negative bands disappeared after depletion of bicarbonate. The addition of bicarbonate partially restored those bands again. Comparison between difference FT-IR spectra of untreated and bicarbonate-depleted PSII membranes indicated that the positive bands at 1589 and 1365 cm−1 can be assigned to COO− stretching modes from bicarbonate. The higher frequency corresponds to uas (COO−) and the lower frequency to us (COO−). 13C-Labeling FT-IR measurements confirmed these findings and also suggested that the negative band at 1560 cm−1 can be ascribed to uas (COO−). The data are discussed in the framework of the suggestion that bicarbonate can be a ligand to the Mn-containing water-oxidizing complex of PSII.
【 授权许可】
Unknown
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