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Double Mutation in Photosystem II Reaction Centers and Elevated CO(2) Grant Thermotolerance to Mesophilic Cyanobacterium

Photosynthetic biomass production rapidly declines in mesophilic cyanobacteria grown above their physiological temperatures largely due to the imbalance between degradation and repair of the D1 protein subunit of the heat susceptible Photosystem II reaction centers (PSIIRC). Here we show that simult...

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Autores principales: Dinamarca, Jorge, Shlyk-Kerner, Oksana, Kaftan, David, Goldberg, Eran, Dulebo, Alexander, Gidekel, Manuel, Gutierrez, Ana, Scherz, Avigdor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245225/
https://www.ncbi.nlm.nih.gov/pubmed/22216094
http://dx.doi.org/10.1371/journal.pone.0028389
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author Dinamarca, Jorge
Shlyk-Kerner, Oksana
Kaftan, David
Goldberg, Eran
Dulebo, Alexander
Gidekel, Manuel
Gutierrez, Ana
Scherz, Avigdor
author_facet Dinamarca, Jorge
Shlyk-Kerner, Oksana
Kaftan, David
Goldberg, Eran
Dulebo, Alexander
Gidekel, Manuel
Gutierrez, Ana
Scherz, Avigdor
author_sort Dinamarca, Jorge
collection PubMed
description Photosynthetic biomass production rapidly declines in mesophilic cyanobacteria grown above their physiological temperatures largely due to the imbalance between degradation and repair of the D1 protein subunit of the heat susceptible Photosystem II reaction centers (PSIIRC). Here we show that simultaneous replacement of two conserved residues in the D1 protein of the mesophilic Synechocystis sp. PCC 6803, by the analogue residues present in the thermophilic Thermosynechococcus elongatus, enables photosynthetic growth, extensive biomass production and markedly enhanced stability and repair rate of PSIIRC for seven days even at 43°C but only at elevated CO(2) (1%). Under the same conditions, the Synechocystis control strain initially presented very slow growth followed by a decline after 3 days. Change in the thylakoid membrane lipids, namely the saturation of the fatty acids is observed upon incubation for the different strains, but only the double mutant shows a concomitant major change of the enthalpy and entropy for the light activated Q(A) (−)→Q(B) electron transfer, rendering them similar to those of the thermophilic strain. Following these findings, computational chemistry and protein dynamics simulations we propose that the D1 double mutation increases the folding stability of the PSIIRC at elevated temperatures. This, together with the decreased impairment of D1 protein repair under increased CO(2) concentrations result in the observed photothermal tolerance of the photosynthetic machinery in the double mutant
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spelling pubmed-32452252012-01-03 Double Mutation in Photosystem II Reaction Centers and Elevated CO(2) Grant Thermotolerance to Mesophilic Cyanobacterium Dinamarca, Jorge Shlyk-Kerner, Oksana Kaftan, David Goldberg, Eran Dulebo, Alexander Gidekel, Manuel Gutierrez, Ana Scherz, Avigdor PLoS One Research Article Photosynthetic biomass production rapidly declines in mesophilic cyanobacteria grown above their physiological temperatures largely due to the imbalance between degradation and repair of the D1 protein subunit of the heat susceptible Photosystem II reaction centers (PSIIRC). Here we show that simultaneous replacement of two conserved residues in the D1 protein of the mesophilic Synechocystis sp. PCC 6803, by the analogue residues present in the thermophilic Thermosynechococcus elongatus, enables photosynthetic growth, extensive biomass production and markedly enhanced stability and repair rate of PSIIRC for seven days even at 43°C but only at elevated CO(2) (1%). Under the same conditions, the Synechocystis control strain initially presented very slow growth followed by a decline after 3 days. Change in the thylakoid membrane lipids, namely the saturation of the fatty acids is observed upon incubation for the different strains, but only the double mutant shows a concomitant major change of the enthalpy and entropy for the light activated Q(A) (−)→Q(B) electron transfer, rendering them similar to those of the thermophilic strain. Following these findings, computational chemistry and protein dynamics simulations we propose that the D1 double mutation increases the folding stability of the PSIIRC at elevated temperatures. This, together with the decreased impairment of D1 protein repair under increased CO(2) concentrations result in the observed photothermal tolerance of the photosynthetic machinery in the double mutant Public Library of Science 2011-12-22 /pmc/articles/PMC3245225/ /pubmed/22216094 http://dx.doi.org/10.1371/journal.pone.0028389 Text en Dinamarca et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Dinamarca, Jorge
Shlyk-Kerner, Oksana
Kaftan, David
Goldberg, Eran
Dulebo, Alexander
Gidekel, Manuel
Gutierrez, Ana
Scherz, Avigdor
Double Mutation in Photosystem II Reaction Centers and Elevated CO(2) Grant Thermotolerance to Mesophilic Cyanobacterium
title Double Mutation in Photosystem II Reaction Centers and Elevated CO(2) Grant Thermotolerance to Mesophilic Cyanobacterium
title_full Double Mutation in Photosystem II Reaction Centers and Elevated CO(2) Grant Thermotolerance to Mesophilic Cyanobacterium
title_fullStr Double Mutation in Photosystem II Reaction Centers and Elevated CO(2) Grant Thermotolerance to Mesophilic Cyanobacterium
title_full_unstemmed Double Mutation in Photosystem II Reaction Centers and Elevated CO(2) Grant Thermotolerance to Mesophilic Cyanobacterium
title_short Double Mutation in Photosystem II Reaction Centers and Elevated CO(2) Grant Thermotolerance to Mesophilic Cyanobacterium
title_sort double mutation in photosystem ii reaction centers and elevated co(2) grant thermotolerance to mesophilic cyanobacterium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245225/
https://www.ncbi.nlm.nih.gov/pubmed/22216094
http://dx.doi.org/10.1371/journal.pone.0028389
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