Cargando…
Exciton Origin of Color-Tuning in Ca(2+)-Binding Photosynthetic Bacteria
Flexible color adaptation to available ecological niches is vital for the photosynthetic organisms to thrive. Hence, most purple bacteria living in the shade of green plants and algae apply bacteriochlorophyll a pigments to harvest near infra-red light around 850–875 nm. Exceptions are some Ca(2+)-c...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8303132/ https://www.ncbi.nlm.nih.gov/pubmed/34298960 http://dx.doi.org/10.3390/ijms22147338 |
_version_ | 1783727013441306624 |
---|---|
author | Timpmann, Kõu Rätsep, Margus Kangur, Liina Lehtmets, Alexandra Wang-Otomo, Zheng-Yu Freiberg, Arvi |
author_facet | Timpmann, Kõu Rätsep, Margus Kangur, Liina Lehtmets, Alexandra Wang-Otomo, Zheng-Yu Freiberg, Arvi |
author_sort | Timpmann, Kõu |
collection | PubMed |
description | Flexible color adaptation to available ecological niches is vital for the photosynthetic organisms to thrive. Hence, most purple bacteria living in the shade of green plants and algae apply bacteriochlorophyll a pigments to harvest near infra-red light around 850–875 nm. Exceptions are some Ca(2+)-containing species fit to utilize much redder quanta. The physical basis of such anomalous absorbance shift equivalent to ~5.5 kT at ambient temperature remains unsettled so far. Here, by applying several sophisticated spectroscopic techniques, we show that the Ca(2+) ions bound to the structure of LH1 core light-harvesting pigment–protein complex significantly increase the couplings between the bacteriochlorophyll pigments. We thus establish the Ca-facilitated enhancement of exciton couplings as the main mechanism of the record spectral red-shift. The changes in specific interactions such as pigment–protein hydrogen bonding, although present, turned out to be secondary in this regard. Apart from solving the two-decade-old conundrum, these results complement the list of physical principles applicable for efficient spectral tuning of photo-sensitive molecular nano-systems, native or synthetic. |
format | Online Article Text |
id | pubmed-8303132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83031322021-07-25 Exciton Origin of Color-Tuning in Ca(2+)-Binding Photosynthetic Bacteria Timpmann, Kõu Rätsep, Margus Kangur, Liina Lehtmets, Alexandra Wang-Otomo, Zheng-Yu Freiberg, Arvi Int J Mol Sci Article Flexible color adaptation to available ecological niches is vital for the photosynthetic organisms to thrive. Hence, most purple bacteria living in the shade of green plants and algae apply bacteriochlorophyll a pigments to harvest near infra-red light around 850–875 nm. Exceptions are some Ca(2+)-containing species fit to utilize much redder quanta. The physical basis of such anomalous absorbance shift equivalent to ~5.5 kT at ambient temperature remains unsettled so far. Here, by applying several sophisticated spectroscopic techniques, we show that the Ca(2+) ions bound to the structure of LH1 core light-harvesting pigment–protein complex significantly increase the couplings between the bacteriochlorophyll pigments. We thus establish the Ca-facilitated enhancement of exciton couplings as the main mechanism of the record spectral red-shift. The changes in specific interactions such as pigment–protein hydrogen bonding, although present, turned out to be secondary in this regard. Apart from solving the two-decade-old conundrum, these results complement the list of physical principles applicable for efficient spectral tuning of photo-sensitive molecular nano-systems, native or synthetic. MDPI 2021-07-08 /pmc/articles/PMC8303132/ /pubmed/34298960 http://dx.doi.org/10.3390/ijms22147338 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Timpmann, Kõu Rätsep, Margus Kangur, Liina Lehtmets, Alexandra Wang-Otomo, Zheng-Yu Freiberg, Arvi Exciton Origin of Color-Tuning in Ca(2+)-Binding Photosynthetic Bacteria |
title | Exciton Origin of Color-Tuning in Ca(2+)-Binding Photosynthetic Bacteria |
title_full | Exciton Origin of Color-Tuning in Ca(2+)-Binding Photosynthetic Bacteria |
title_fullStr | Exciton Origin of Color-Tuning in Ca(2+)-Binding Photosynthetic Bacteria |
title_full_unstemmed | Exciton Origin of Color-Tuning in Ca(2+)-Binding Photosynthetic Bacteria |
title_short | Exciton Origin of Color-Tuning in Ca(2+)-Binding Photosynthetic Bacteria |
title_sort | exciton origin of color-tuning in ca(2+)-binding photosynthetic bacteria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8303132/ https://www.ncbi.nlm.nih.gov/pubmed/34298960 http://dx.doi.org/10.3390/ijms22147338 |
work_keys_str_mv | AT timpmannkou excitonoriginofcolortuninginca2bindingphotosyntheticbacteria AT ratsepmargus excitonoriginofcolortuninginca2bindingphotosyntheticbacteria AT kangurliina excitonoriginofcolortuninginca2bindingphotosyntheticbacteria AT lehtmetsalexandra excitonoriginofcolortuninginca2bindingphotosyntheticbacteria AT wangotomozhengyu excitonoriginofcolortuninginca2bindingphotosyntheticbacteria AT freibergarvi excitonoriginofcolortuninginca2bindingphotosyntheticbacteria |