| Circular Dichroism of Carotenoids in Bacterial Light-Harvesting Complexes: Experiments and Modeling Biophysical Journal, Volume 87, Issue 5, 1 November 2004, Pages 3010-3022 S. Georgakopoulou, R. van Grondelle and G. van der Zwan Abstract In this work we investigate the origin and characteristics of the circular dichroism (CD) spectrum of rhodopin glucoside and lycopene in the light-harvesting 2 complex of and , respectively. We successfully model their absorption and CD spectra based on the high-resolution structures. We assume that these spectra originate from seven interacting transition dipole moments: the first corresponds to the 0-0 transition of the carotenoid, whereas the remaining six represent higher vibronic components of the S state. From the absorption spectra we get an estimate of the Franck-Condon factors of these transitions. Furthermore, we investigate the broadening mechanisms that lead to the final shape of the spectra and get an insight into the interaction energy between carotenoids. Finally, we examine the consequences of rotations of the carotenoid transition dipole moment and of deformations in the light-harvesting 2 complex rings. Comparison of the modeled carotenoid spectra with modeled spectra of the bacteriochlorophyll Q region leads to a refinement of the modeling procedure and an improvement of all calculated results. We therefore propose that the combined carotenoid and bacteriochlorophyll CD can be used as an accurate reflection of the overall structure of the light-harvesting complexes. Abstract | Full Text | PDF (263 kb) |
| Pigment–pigment interactions and energy transfer in the antenna complex of the photosynthetic bacterium Rhodopseudomonasacidophila Structure, Volume 4, Issue 4, 1 April 1996, Pages 449-462 Andy Freer, Steve Prince, Ken Sauer, Miroslav Papiz, Anna Hawthornthwaite Lawless, Gerry McDermott, Richard Cogdell and Neil W Isaacs Summary The structure of the antenna complex not only shows Nature at its most aesthetic but also illustrates how clever and efficient the energy transfer mechanism has become, with singlet–singlet excitation being passed smoothly down the spectral gradient to the reaction centre. Summary | Full Text | PDF (983 kb) |
| Energy Transfer in the Peridinin Chlorophyll-a Protein of Amphidinium carterae Studied by Polarized Transient Absorption and Target Analysis Biophysical Journal, Volume 80, Issue 6, 1 June 2001, Pages 2843-2855 Brent P. Krueger, Stefania S. Lampoura, Ivo H.M. van Stokkum, Emmanouil Papagiannakis, Jante M. Salverda, Claudiu C. Gradinaru, Danielis Rutkauskas, Roger G. Hiller and Rienk van Grondelle Abstract The peridinin chlorophyll- protein (PCP) of dinoflagellates differs from the well-studied light-harvesting complexes of purple bacteria and green plants in its large (4:1) carotenoid to chlorophyll ratio and the unusual properties of its primary pigment, the carotenoid peridinin. We utilized ultrafast polarized transient absorption spectroscopy to examine the flow of energy in PCP after initial excitation into the strongly allowed peridinin S state. Global and target analysis of the isotropic and anisotropic decays reveals that significant excitation (25–50%) is transferred to chlorophyll- directly from the peridinin S state. Because of overlapping positive and negative features, this pathway was unseen in earlier single-wavelength experiments. In addition, the anisotropy remains constant and high in the peridinin population, indicating that energy transfer from peridinin to peridinin represents a minor or negligible pathway. The carotenoids are also coupled directly to chlorophyll- via a low-lying singlet state S or the recently identified S. We model this energy transfer time scale as 2.3±0.2ps, driven by a coupling of ∼47cm. This coupling strength allows us to estimate that the peridinin S/S donor state transition moment is ∼3 D. Abstract | Full Text | PDF (249 kb) |
Copyright © 1982 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 39, Issue 1, 57-63, 1 July 1982
doi:10.1016/S0006-3495(82)84490-1
Research Article
T. Kakitani, B. Honig and A.R. Crofts
Molecular orbital calculations are carried out on a number of carotenoids in the presence of an external charge and a constant electric field. The external charge is used to represent the strong permanent field that is believed to polarize carotenoids in photosynthetic membranes and thus to account for their linear response to the transmembrane potential. Our calculations show that the in vitro leads to in vivo spectral shifts of carotenoids (approximately 25 nm) can be produced by a charge in close proximity to the molecule. The interaction of the induced dipole moment with a constant field accounts for the observed magnitude of the electrochromic response in photosynthetic bacteria. The existence of a second pool of carotenoids that shows a significant (approximately 20 nm) wavelength shift but no electrochromic response can be explained by an external charge positioned near the center of the molecule that affects its absorption maximum while inducing essentially no dipole moment. The spectral shift for this pool is due to the induction of higher multipoles. These also account for discrepancies that arise when one attempts to account quantitatively for available experimental results on carotenoid band shifts in terms of classical electrochromic theory.