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Evidence for reversible light-dependent transitions in the photosynthetic pigments of diatoms

Marine diatoms contribute to oxygenic photosynthesis and carbon fixation and handle large changes under variable light intensity on a regular basis. The unique light-harvesting apparatus of diatoms are the fucoxanthin–chlorophyll a/c-binding proteins (FCPs). Here, we show the enhancement of chloroph...

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Autores principales: Tselios, Charalampos, Varotsis, Constantinos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631684/
https://www.ncbi.nlm.nih.gov/pubmed/36380945
http://dx.doi.org/10.1039/d2ra05284a
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author Tselios, Charalampos
Varotsis, Constantinos
author_facet Tselios, Charalampos
Varotsis, Constantinos
author_sort Tselios, Charalampos
collection PubMed
description Marine diatoms contribute to oxygenic photosynthesis and carbon fixation and handle large changes under variable light intensity on a regular basis. The unique light-harvesting apparatus of diatoms are the fucoxanthin–chlorophyll a/c-binding proteins (FCPs). Here, we show the enhancement of chlorophyll a/c (Chl a/c), fucoxanthin (Fx), and diadinoxanthin (Dd) marker bands in the Raman spectra of the centric diatom T. pseudonana, which allows distinction of the pigment content in the cells grown under low- (LL) and high-light (HL) intensity at room temperature. Reversible LL–HL dependent conformations of Chl c, characteristic of two conformations of the porphyrin macrocycle, and the presence of five- and six-coordinated Chl a/c with weak axial ligands are observed in the Raman data. Under HL the energy transfer from Chl c to Chl a is reduced and that from the red-shifted Fxs is minimal. Therefore, Chl c and the blue-shifted Fxs are the only contributors to the energy transfer pathways under HL and the blue- to red-shifted Fxs energy transfer pathway characteristic of the LL is inactive. The results indicate that T. pseudonana can redirect its function from light harvesting to energy-quenching state, and reversibly to light-harvesting upon subsequent illumination to LL by reproducing the red-shifted Fxs and decrease the number of Dds. The LL to HL reversible transitions are accompanied by structural modifications of Chl a/c and the lack of the red-shifted Fxs.
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spelling pubmed-96316842022-11-14 Evidence for reversible light-dependent transitions in the photosynthetic pigments of diatoms Tselios, Charalampos Varotsis, Constantinos RSC Adv Chemistry Marine diatoms contribute to oxygenic photosynthesis and carbon fixation and handle large changes under variable light intensity on a regular basis. The unique light-harvesting apparatus of diatoms are the fucoxanthin–chlorophyll a/c-binding proteins (FCPs). Here, we show the enhancement of chlorophyll a/c (Chl a/c), fucoxanthin (Fx), and diadinoxanthin (Dd) marker bands in the Raman spectra of the centric diatom T. pseudonana, which allows distinction of the pigment content in the cells grown under low- (LL) and high-light (HL) intensity at room temperature. Reversible LL–HL dependent conformations of Chl c, characteristic of two conformations of the porphyrin macrocycle, and the presence of five- and six-coordinated Chl a/c with weak axial ligands are observed in the Raman data. Under HL the energy transfer from Chl c to Chl a is reduced and that from the red-shifted Fxs is minimal. Therefore, Chl c and the blue-shifted Fxs are the only contributors to the energy transfer pathways under HL and the blue- to red-shifted Fxs energy transfer pathway characteristic of the LL is inactive. The results indicate that T. pseudonana can redirect its function from light harvesting to energy-quenching state, and reversibly to light-harvesting upon subsequent illumination to LL by reproducing the red-shifted Fxs and decrease the number of Dds. The LL to HL reversible transitions are accompanied by structural modifications of Chl a/c and the lack of the red-shifted Fxs. The Royal Society of Chemistry 2022-11-03 /pmc/articles/PMC9631684/ /pubmed/36380945 http://dx.doi.org/10.1039/d2ra05284a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Tselios, Charalampos
Varotsis, Constantinos
Evidence for reversible light-dependent transitions in the photosynthetic pigments of diatoms
title Evidence for reversible light-dependent transitions in the photosynthetic pigments of diatoms
title_full Evidence for reversible light-dependent transitions in the photosynthetic pigments of diatoms
title_fullStr Evidence for reversible light-dependent transitions in the photosynthetic pigments of diatoms
title_full_unstemmed Evidence for reversible light-dependent transitions in the photosynthetic pigments of diatoms
title_short Evidence for reversible light-dependent transitions in the photosynthetic pigments of diatoms
title_sort evidence for reversible light-dependent transitions in the photosynthetic pigments of diatoms
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631684/
https://www.ncbi.nlm.nih.gov/pubmed/36380945
http://dx.doi.org/10.1039/d2ra05284a
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