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Identification of distinct pH- and zeaxanthin-dependent quenching in LHCSR3 from Chlamydomonas reinhardtii

Under high light, oxygenic photosynthetic organisms avoid photodamage by thermally dissipating absorbed energy, which is called nonphotochemical quenching. In green algae, a chlorophyll and carotenoid-binding protein, light-harvesting complex stress-related (LHCSR3), detects excess energy via a pH d...

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Autores principales: Troiano, Julianne M, Perozeni, Federico, Moya, Raymundo, Zuliani, Luca, Baek, Kwangyrul, Jin, EonSeon, Cazzaniga, Stefano, Ballottari, Matteo, Schlau-Cohen, Gabriela S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864637/
https://www.ncbi.nlm.nih.gov/pubmed/33448262
http://dx.doi.org/10.7554/eLife.60383
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author Troiano, Julianne M
Perozeni, Federico
Moya, Raymundo
Zuliani, Luca
Baek, Kwangyrul
Jin, EonSeon
Cazzaniga, Stefano
Ballottari, Matteo
Schlau-Cohen, Gabriela S
author_facet Troiano, Julianne M
Perozeni, Federico
Moya, Raymundo
Zuliani, Luca
Baek, Kwangyrul
Jin, EonSeon
Cazzaniga, Stefano
Ballottari, Matteo
Schlau-Cohen, Gabriela S
author_sort Troiano, Julianne M
collection PubMed
description Under high light, oxygenic photosynthetic organisms avoid photodamage by thermally dissipating absorbed energy, which is called nonphotochemical quenching. In green algae, a chlorophyll and carotenoid-binding protein, light-harvesting complex stress-related (LHCSR3), detects excess energy via a pH drop and serves as a quenching site. Using a combined in vivo and in vitro approach, we investigated quenching within LHCSR3 from Chlamydomonas reinhardtii. In vitro two distinct quenching processes, individually controlled by pH and zeaxanthin, were identified within LHCSR3. The pH-dependent quenching was removed within a mutant LHCSR3 that lacks the residues that are protonated to sense the pH drop. Observation of quenching in zeaxanthin-enriched LHCSR3 even at neutral pH demonstrated zeaxanthin-dependent quenching, which also occurs in other light-harvesting complexes. Either pH- or zeaxanthin-dependent quenching prevented the formation of damaging reactive oxygen species, and thus the two quenching processes may together provide different induction and recovery kinetics for photoprotection in a changing environment.
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spelling pubmed-78646372021-02-08 Identification of distinct pH- and zeaxanthin-dependent quenching in LHCSR3 from Chlamydomonas reinhardtii Troiano, Julianne M Perozeni, Federico Moya, Raymundo Zuliani, Luca Baek, Kwangyrul Jin, EonSeon Cazzaniga, Stefano Ballottari, Matteo Schlau-Cohen, Gabriela S eLife Plant Biology Under high light, oxygenic photosynthetic organisms avoid photodamage by thermally dissipating absorbed energy, which is called nonphotochemical quenching. In green algae, a chlorophyll and carotenoid-binding protein, light-harvesting complex stress-related (LHCSR3), detects excess energy via a pH drop and serves as a quenching site. Using a combined in vivo and in vitro approach, we investigated quenching within LHCSR3 from Chlamydomonas reinhardtii. In vitro two distinct quenching processes, individually controlled by pH and zeaxanthin, were identified within LHCSR3. The pH-dependent quenching was removed within a mutant LHCSR3 that lacks the residues that are protonated to sense the pH drop. Observation of quenching in zeaxanthin-enriched LHCSR3 even at neutral pH demonstrated zeaxanthin-dependent quenching, which also occurs in other light-harvesting complexes. Either pH- or zeaxanthin-dependent quenching prevented the formation of damaging reactive oxygen species, and thus the two quenching processes may together provide different induction and recovery kinetics for photoprotection in a changing environment. eLife Sciences Publications, Ltd 2021-01-15 /pmc/articles/PMC7864637/ /pubmed/33448262 http://dx.doi.org/10.7554/eLife.60383 Text en © 2021, Troiano et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Plant Biology
Troiano, Julianne M
Perozeni, Federico
Moya, Raymundo
Zuliani, Luca
Baek, Kwangyrul
Jin, EonSeon
Cazzaniga, Stefano
Ballottari, Matteo
Schlau-Cohen, Gabriela S
Identification of distinct pH- and zeaxanthin-dependent quenching in LHCSR3 from Chlamydomonas reinhardtii
title Identification of distinct pH- and zeaxanthin-dependent quenching in LHCSR3 from Chlamydomonas reinhardtii
title_full Identification of distinct pH- and zeaxanthin-dependent quenching in LHCSR3 from Chlamydomonas reinhardtii
title_fullStr Identification of distinct pH- and zeaxanthin-dependent quenching in LHCSR3 from Chlamydomonas reinhardtii
title_full_unstemmed Identification of distinct pH- and zeaxanthin-dependent quenching in LHCSR3 from Chlamydomonas reinhardtii
title_short Identification of distinct pH- and zeaxanthin-dependent quenching in LHCSR3 from Chlamydomonas reinhardtii
title_sort identification of distinct ph- and zeaxanthin-dependent quenching in lhcsr3 from chlamydomonas reinhardtii
topic Plant Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864637/
https://www.ncbi.nlm.nih.gov/pubmed/33448262
http://dx.doi.org/10.7554/eLife.60383
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