The role of vibronic modes in formation of red antenna states of cyanobacterial PSI

Cyanobacterial photosystem I (PSI) constitutes monomeric and trimeric pigment–protein complexes whose optical properties are marked by the presence of long-wavelength absorption bands. In spite of numerous experimental studies, the nature of these bands is still under debate and requires intensive t...

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Veröffentlicht in:Photosynthesis research 2020-12, Vol.146 (1-3), p.75-86
Hauptverfasser: Pishchalnikov, Roman Y., Shubin, Vladimir. V., Razjivin, Andrei. P.
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Sprache:eng
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Zusammenfassung:Cyanobacterial photosystem I (PSI) constitutes monomeric and trimeric pigment–protein complexes whose optical properties are marked by the presence of long-wavelength absorption bands. In spite of numerous experimental studies, the nature of these bands is still under debate and requires intensive theoretical analysis. Collecting together the data of linear spectroscopy and single-molecule spectroscopy (SMS) of PSI from Arthrospira platensis , we performed quantum modeling of the optical response based on molecular exciton theory (ET) and the multimode Brownian oscillator model (MBOM). Applying MBOM, the spectra of the red antenna state were calculated considering a particular for each red state adjustment of the low-frequency vibronic modes. Within the framework of our PSI exciton model it was shown that the coupling energy between antenna chlorophylls cannot be a factor of the red states formation, thus the long-wavelength bands are calculated without attribution to so-called antenna red chlorophylls. By the fitting of Huang–Rhys factors and frequencies for the lowest vibronic modes, we were able to reproduce the effects of strong and weak electron–phonon coupling experimentally observed in SMS spectra of red antenna states. Based on our theoretical calculations and also analysis of existing crystal structures of cyanobacterial PSI, we assumed that long-wavelength Chls can be localized in the peripheral protein subunits containing one or two pigment molecules.
ISSN:0166-8595
1573-5079
DOI:10.1007/s11120-020-00779-y