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Issue 13, 2019
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Absorption shifts of diastereotopically ligated chlorophyll dimers of photosystem I

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Abstract

The light-harvesting chlorophyll (Chl) molecules of photosynthetic systems form the basis for light-driven energy conversion. In biological environments, the Chl chromophores occur in two distinct diastereotopic configurations, where the α and β configurations have a magnesium-ligating histidine residue and a 17-propionic acid moiety on the opposite side or on the same side of the Chl ring, respectively. Although β-ligated Chl dimers occupy conserved positions around the reaction center of photosystem I (PSI), the functional relevance of the α/β configuration of the ligation is poorly understood. We employ here correlated ab initio calculations using the algebraic-diagrammatic construction through second order (ADC(2)) and the approximate second-order coupled cluster (CC2) methods in combination with the reduced virtual space (RVS) approach in studies of the intrinsic excited-state properties of α-ligated and β-ligated Chl dimers of PSI. Our ab initio calculations suggest that the absorption of the α-ligated reaction-center Chl dimer of PSI is redshifted by 0.13–0.14 eV in comparison to the β-ligated dimers due to combined excitonic coupling and strain effects. We also show that time-dependent density functional theory (TDDFT) calculations using range-separated density functionals underestimate the absorption shift between the α- and β-ligated dimers. Our findings may provide a molecular starting point for understanding the energy flow in natural photosynthetic systems, as well as a blueprint for developing new molecules that convert sunlight into other forms of energy.

Graphical abstract: Absorption shifts of diastereotopically ligated chlorophyll dimers of photosystem I

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Supplementary files

Article information


Submitted
31 Jan 2019
Accepted
08 Mar 2019
First published
11 Mar 2019

This article is Open Access

Phys. Chem. Chem. Phys., 2019,21, 6851-6858
Article type
Paper

Absorption shifts of diastereotopically ligated chlorophyll dimers of photosystem I

C. Suomivuori, H. Fliegl, E. B. Starikov, T. S. Balaban, V. R. I. Kaila and D. Sundholm, Phys. Chem. Chem. Phys., 2019, 21, 6851
DOI: 10.1039/C9CP00616H

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