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Picosecond excitation energy transfer of allophycocyanin studied in solution and in crystals

Cyanobacteria perform photosynthesis with the use of large light-harvesting antennae called phycobilisomes (PBSs). These hemispherical PBSs contain hundreds of open-chain tetrapyrrole chromophores bound to different peptides, providing an arrangement in which excitation energy is funnelled towards t...

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Autores principales: Ranjbar Choubeh, Reza, Sonani, Ravi R., Madamwar, Datta, Struik, Paul C., Bader, Arjen N., Robert, Bruno, van Amerongen, Herbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783994/
https://www.ncbi.nlm.nih.gov/pubmed/28755150
http://dx.doi.org/10.1007/s11120-017-0417-4
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author Ranjbar Choubeh, Reza
Sonani, Ravi R.
Madamwar, Datta
Struik, Paul C.
Bader, Arjen N.
Robert, Bruno
van Amerongen, Herbert
author_facet Ranjbar Choubeh, Reza
Sonani, Ravi R.
Madamwar, Datta
Struik, Paul C.
Bader, Arjen N.
Robert, Bruno
van Amerongen, Herbert
author_sort Ranjbar Choubeh, Reza
collection PubMed
description Cyanobacteria perform photosynthesis with the use of large light-harvesting antennae called phycobilisomes (PBSs). These hemispherical PBSs contain hundreds of open-chain tetrapyrrole chromophores bound to different peptides, providing an arrangement in which excitation energy is funnelled towards the PBS core from where it can be transferred to photosystem I and/or photosystem II. In the PBS core, many allophycocyanin (APC) trimers are present, red-light-absorbing phycobiliproteins that covalently bind phycocyanobilin (PCB) chromophores. APC trimers were amongst the first light-harvesting complexes to be crystallized. APC trimers have two spectrally different PCBs per monomer, a high- and a low-energy pigment. The crystal structure of the APC trimer reveals the close distance (~21 Å) between those two chromophores (the distance within one monomer is ~51 Å) and this explains the ultrafast (~1 ps) excitation energy transfer (EET) between them. Both chromophores adopt a somewhat different structure, which is held responsible for their spectral difference. Here we used spectrally resolved picosecond fluorescence to study EET in these APC trimers both in crystallized and in solubilized form. We found that not all closely spaced pigment couples consist of a low- and a high-energy pigment. In ~10% of the cases, a couple consists of two high-energy pigments. EET to a low-energy pigment, which can spectrally be resolved, occurs on a time scale of tens of picoseconds. This transfer turns out to be three times faster in the crystal than in the solution. The spectral characteristics and the time scale of this transfer component are similar to what have been observed in the whole cells of Synechocystis sp. PCC 6803, for which it was ascribed to EET from C-phycocyanin to APC. The present results thus demonstrate that part of this transfer should probably also be ascribed to EET within APC trimers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11120-017-0417-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-57839942018-02-01 Picosecond excitation energy transfer of allophycocyanin studied in solution and in crystals Ranjbar Choubeh, Reza Sonani, Ravi R. Madamwar, Datta Struik, Paul C. Bader, Arjen N. Robert, Bruno van Amerongen, Herbert Photosynth Res Original Article Cyanobacteria perform photosynthesis with the use of large light-harvesting antennae called phycobilisomes (PBSs). These hemispherical PBSs contain hundreds of open-chain tetrapyrrole chromophores bound to different peptides, providing an arrangement in which excitation energy is funnelled towards the PBS core from where it can be transferred to photosystem I and/or photosystem II. In the PBS core, many allophycocyanin (APC) trimers are present, red-light-absorbing phycobiliproteins that covalently bind phycocyanobilin (PCB) chromophores. APC trimers were amongst the first light-harvesting complexes to be crystallized. APC trimers have two spectrally different PCBs per monomer, a high- and a low-energy pigment. The crystal structure of the APC trimer reveals the close distance (~21 Å) between those two chromophores (the distance within one monomer is ~51 Å) and this explains the ultrafast (~1 ps) excitation energy transfer (EET) between them. Both chromophores adopt a somewhat different structure, which is held responsible for their spectral difference. Here we used spectrally resolved picosecond fluorescence to study EET in these APC trimers both in crystallized and in solubilized form. We found that not all closely spaced pigment couples consist of a low- and a high-energy pigment. In ~10% of the cases, a couple consists of two high-energy pigments. EET to a low-energy pigment, which can spectrally be resolved, occurs on a time scale of tens of picoseconds. This transfer turns out to be three times faster in the crystal than in the solution. The spectral characteristics and the time scale of this transfer component are similar to what have been observed in the whole cells of Synechocystis sp. PCC 6803, for which it was ascribed to EET from C-phycocyanin to APC. The present results thus demonstrate that part of this transfer should probably also be ascribed to EET within APC trimers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11120-017-0417-4) contains supplementary material, which is available to authorized users. Springer Netherlands 2017-07-28 2018 /pmc/articles/PMC5783994/ /pubmed/28755150 http://dx.doi.org/10.1007/s11120-017-0417-4 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Ranjbar Choubeh, Reza
Sonani, Ravi R.
Madamwar, Datta
Struik, Paul C.
Bader, Arjen N.
Robert, Bruno
van Amerongen, Herbert
Picosecond excitation energy transfer of allophycocyanin studied in solution and in crystals
title Picosecond excitation energy transfer of allophycocyanin studied in solution and in crystals
title_full Picosecond excitation energy transfer of allophycocyanin studied in solution and in crystals
title_fullStr Picosecond excitation energy transfer of allophycocyanin studied in solution and in crystals
title_full_unstemmed Picosecond excitation energy transfer of allophycocyanin studied in solution and in crystals
title_short Picosecond excitation energy transfer of allophycocyanin studied in solution and in crystals
title_sort picosecond excitation energy transfer of allophycocyanin studied in solution and in crystals
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783994/
https://www.ncbi.nlm.nih.gov/pubmed/28755150
http://dx.doi.org/10.1007/s11120-017-0417-4
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