Molecular events accompanying aggregation-induced energy quenching in fucoxanthin-chlorophyll proteins.

Diatoms Light-harvesting NPQ Photoprotection Raman Xanthophyll

Journal

Biochimica et biophysica acta. Bioenergetics
ISSN: 1879-2650
Titre abrégé: Biochim Biophys Acta Bioenerg
Pays: Netherlands
ID NLM: 101731706

Informations de publication

Date de publication:
27 Jul 2024
Historique:
received: 05 04 2024
revised: 21 07 2024
accepted: 26 07 2024
medline: 30 7 2024
pubmed: 30 7 2024
entrez: 29 7 2024
Statut: aheadofprint

Résumé

In high light, the antenna system in oxygenic photosynthetic organisms switches to a photoprotective mode, dissipating excess energy in a process called non-photochemical quenching (NPQ). Diatoms exhibit very efficient NPQ, accompanied by a xanthophyll cycle in which diadinoxanthin is de-epoxidized into diatoxanthin. Diatoms accumulate pigments from this cycle in high light, and exhibit faster and more pronounced NPQ. The mechanisms underlying NPQ in diatoms remain unclear, but it can be mimicked by aggregation of their isolated light-harvesting complexes, FCP (fucoxanthin chlorophyll-a/c protein). We assess this model system by resonance Raman measurements of two peripheral FCPs, trimeric FCPa and nonameric FCPb, isolated from high- and low-light-adapted cells (LL,HL). Quenching is associated with a reorganisation of these proteins, affecting the conformation of their bound carotenoids, and in a manner which is highly dependent on the protein considered. FCPa from LL diatoms exhibits significant changes in diadinoxanthin structure, together with a smaller conformational change of at least one fucoxanthin. For these LL-FCPa, quenching is associated with consecutive events, displaying distinct spectral signatures, and its amplitude correlates with the planarity of the diadinoxanthin structure. HL-FCPa aggregation is associated with a change in planarity of a 515-nm-absorbing fucoxanthin, and, to a lesser extent, of diadinoxanthin. Finally, in FCPb, a blue-absorbing fucoxanthin is primarily affected. FCPs thus possess a plastic structure, undergoing several conformational changes upon aggregation, dependent upon their precise composition and structure. NPQ in diatoms may therefore arise from a combination of structural changes, dependent on the environment the cells are adapted to.

Identifiants

pubmed: 39074571
pii: S0005-2728(24)00470-5
doi: 10.1016/j.bbabio.2024.149500
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

149500

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Maxime T A Alexandre (MTA)

Institute of Integrative Biology of the Cell, CEA, CNRS, Université Paris-Saclay, Avenue de la Terrasse, 91198 Gif sur Yvette, France; Department of Physics and Astronomy, Faculty of Sciences, VU University Amsterdam, De Boelelaan, 1081 HV Amsterdam, the Netherlands.

Tjaart P J Krüger (TPJ)

Department of Physics, Forestry and Agricultural Biotechnology Institute (FABI), Faculty of Natural and Agricultural Sciences, University of Pretoria, Private bag X20, Hatfield 0028, South Africa.

Andrew A Pascal (AA)

Institute of Integrative Biology of the Cell, CEA, CNRS, Université Paris-Saclay, Avenue de la Terrasse, 91198 Gif sur Yvette, France. Electronic address: andrew.pascal@i2bc.paris-saclay.fr.

Vasyl Veremeienko (V)

Institute of Integrative Biology of the Cell, CEA, CNRS, Université Paris-Saclay, Avenue de la Terrasse, 91198 Gif sur Yvette, France.

Manuel Llansola-Portoles (M)

Institute of Integrative Biology of the Cell, CEA, CNRS, Université Paris-Saclay, Avenue de la Terrasse, 91198 Gif sur Yvette, France.

Kathi Gundermann (K)

Institute of Molecular Biosciences, Department of Biosciences, Goethe University Frankfurt, Max von Laue Str. 9, 60438 Frankfurt, Germany.

Rienk van Grondelle (R)

Department of Physics and Astronomy, Faculty of Sciences, VU University Amsterdam, De Boelelaan, 1081 HV Amsterdam, the Netherlands.

Claudia Büchel (C)

Institute of Molecular Biosciences, Department of Biosciences, Goethe University Frankfurt, Max von Laue Str. 9, 60438 Frankfurt, Germany.

Bruno Robert (B)

Institute of Integrative Biology of the Cell, CEA, CNRS, Université Paris-Saclay, Avenue de la Terrasse, 91198 Gif sur Yvette, France.

Classifications MeSH