FTIR spectroscopy of primary donor photooxidation in Photosystem I, Heliobacillus mobilis, and Chlorobium limicola. Comparison with purple bacteria
- 1 May 1996
- journal article
- Published by Springer Nature in Photosynthesis Research
- Vol. 48 (1-2) , 301-308
- https://doi.org/10.1007/bf00041021
Abstract
The photooxidation of the primary electron donor in several Photosystem I-related organisms (Synechocystis sp. PCC 6803, Heliobacillus mobilis, and Chlorobium limicola f. sp. thiosulphatophilum) has been studied by light-induced FTIR difference spectroscopy at 100 K in the 4000 to 1200 cm−1 spectral range. The data are compared to the well-characterized FTIR difference spectra of the photooxidation of the primary donor P in Rhodobacter sphaeroides (both wild type and the heterodimer mutant HL M202) in order to get information on the charge localization and the extent of coupling within the (bacterio)chlorophylls constituting the oxidized primary donors. In Rb. sphaeroides RC, four marker bands mostly related to the dimeric nature of the oxidized primary donor have been previously observed at ≈2600, 1550, 1480, and 1295 cm−1. The high-frequency band has been shown to correspond to an electronic transition (Breton et al. (1992) Biochemistry 31: 7503–7510) while the three other marker bands have been described as phase-phonon bands (Reimers and Hush (1995) Chem Phys 197: 323–332). The absence of these bands in PS I as well as in the heterodimer HL M202 demonstrates that in P700+ the charge is essentially localized on a single chlorophyll molecule. For both H. mobilis and C. limicola, the presence of a high-frequency band at ≈ 2050 and 2450 cm−1, respectively, and of phase-phonon bands (at ≈ 1535 and 1300 cm−1 in H. mobilis, at ≈ 1465 and 1280 cm-1 in C. limicola) indicate that the positive charge in the photooxidized primary donor is shared between two coupled BChls. The structure of P840+ in C. limicola, in terms of the resonance interactions between the two BChl a molecules constituting the oxidized primary donor, is close to that of P+ in purple bacteria reaction centers while for H. mobilis the FTIR data are interpreted in terms of a weaker coupling of the two bacteriochlorophylls.Keywords
This publication has 37 references indexed in Scilit:
- The electronic structure of P840+• The primary donor of the Chlorobium limicola f. sp. thiosulphatophilum photosynthetic reaction centreFEBS Letters, 1994
- The Binding Sites of Quinones in Photosynthetic Bacterial Reaction Centers Investigated by Light-Induced FTIR Difference Spectroscopy: Assignment of the QA Vibrations in Rhodobacter sphaeroides Using 18O- or 13C-Labeled Ubiquinones and Vitamin K1Biochemistry, 1994
- Fourier transform infrared study of the primary electron donor in chromatophores of Rhodobacter sphaeroides with reaction centers genetically modified at residues M160 and L131Biochemistry, 1993
- The origin of infrared marker bands of porphyrin .pi.-cation radicals: infrared assignments for cations of copper(II) complexes of octaethylporphine and tetraphenylporphineJournal of the American Chemical Society, 1993
- Hole localization and spin coupling in .pi.-mono- and .pi.-dications of .mu.-oxoporphyrin dimers. Relevance to structure of oxidized special pair in photosynthetic reaction centersThe Journal of Physical Chemistry, 1993
- The electronic structure of the primary donor cation radical in Rhodobacter sphaeroides R-26: ENDOR and TRIPLE resonance studies in single crystals of reaction centersBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1993
- Modulation analysis of the electron spin echo signals of in vivo oxidised primary donor 14N chlorophyll centres in bacterial, P870 and P960, and plant Photosystem I, P700, reaction centresBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1993
- Three-dimensional structure of system I of photosynthesis at 6 Å resolutionNature, 1993
- A protein conformational change associated with the photoreduction of the primary and secondary quinones in the bacterial reaction centerFEBS Letters, 1990
- Light‐induced Fourier transform infrared (FTIR) spectroscopic investigations of primary reactions in photosystem I and photosystem IIFEBS Letters, 1986