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Palmelloid formation in the Antarctic psychrophile, Chlamydomonas priscuii, is photoprotective

Cultures of the obligate, Antarctic psychrophile, Chlamydomonas priscuii grown at permissive low temperature (8°C) are composed of flagellated, single cells, as well as non-motile, multicellular palmelloids. The relative proportions of the two cell types are temperature dependent. However, the tempe...

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Autores principales: Szyszka-Mroz, Beth, Ivanov, Alexander G., Trick, Charles G., Hüner, Norman P. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9470844/
https://www.ncbi.nlm.nih.gov/pubmed/36119589
http://dx.doi.org/10.3389/fpls.2022.911035
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author Szyszka-Mroz, Beth
Ivanov, Alexander G.
Trick, Charles G.
Hüner, Norman P. A.
author_facet Szyszka-Mroz, Beth
Ivanov, Alexander G.
Trick, Charles G.
Hüner, Norman P. A.
author_sort Szyszka-Mroz, Beth
collection PubMed
description Cultures of the obligate, Antarctic psychrophile, Chlamydomonas priscuii grown at permissive low temperature (8°C) are composed of flagellated, single cells, as well as non-motile, multicellular palmelloids. The relative proportions of the two cell types are temperature dependent. However, the temperature dependence for palmelloid formation is not restricted to psychrophilic C. priscuii but appears to be a general response of mesophilic Chlamydomonas species (C. reinhardtii and C. raudensis) to non-permissive growth temperatures. To examine potential differences in photosynthetic performance between single cells versus palmelloids of the psychrophile, a cell filtration technique was developed to separate single cells from palmelloids of C. priscuii grown at 8°C. Flow cytometry was used to estimate the diameter of isolated single cells (≤5 μm) versus isolated palmelloids of varying size (≥8 μm). Compared to single cells, palmelloids of C. priscuii showed a decrease in the abundance of light-harvesting complex II (LHCII) proteins with a 2-fold higher Chl a/b ratio. A decrease in both lutein and β-carotene in palmelloids resulted in carotenoid pools which were 27% lower in palmelloids compared to single cells of the psychrophile. Chlorophyll fluorescence analyses of the isolated fractions revealed that maximum photochemical efficiency of PSII (F(v)/F(m)) was comparable for both single cells and palmelloids of C. priscuii. However, isolated palmelloids exhibited lower excitation pressure, measured as 1 - qL, but higher yield of PSII (Φ(PSII)) and 50% higher rates of electron transport (ETR) than single cells exposed to high light at 8°C. This decreased sensitivity to high light in isolated palmelloids compared to single cells was associated with greater non-regulated dissipation of excess absorbed energy (Φ(NO)) with minimal differences in Φ(NPQ) in C. priscuii in response to increasing irradiance at low temperature. The ratio Φ(NO)/Φ(NPQ) observed for isolated palmelloids of C. priscuii developed at 8°C (1.414 ± 0.036) was 1.38-fold higher than Φ(NO)/Φ(NPQ) of isolated single cells (1.021 ± 0.018) exposed to low temperature combined with high light (1,000 μmol m(−2) s(−1)). The differences in the energy quenching capacities between palmelloids and single cells are discussed in terms of enhanced photoprotection of C. priscuii palmelloids against low-temperature photoinhibition.
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spelling pubmed-94708442022-09-15 Palmelloid formation in the Antarctic psychrophile, Chlamydomonas priscuii, is photoprotective Szyszka-Mroz, Beth Ivanov, Alexander G. Trick, Charles G. Hüner, Norman P. A. Front Plant Sci Plant Science Cultures of the obligate, Antarctic psychrophile, Chlamydomonas priscuii grown at permissive low temperature (8°C) are composed of flagellated, single cells, as well as non-motile, multicellular palmelloids. The relative proportions of the two cell types are temperature dependent. However, the temperature dependence for palmelloid formation is not restricted to psychrophilic C. priscuii but appears to be a general response of mesophilic Chlamydomonas species (C. reinhardtii and C. raudensis) to non-permissive growth temperatures. To examine potential differences in photosynthetic performance between single cells versus palmelloids of the psychrophile, a cell filtration technique was developed to separate single cells from palmelloids of C. priscuii grown at 8°C. Flow cytometry was used to estimate the diameter of isolated single cells (≤5 μm) versus isolated palmelloids of varying size (≥8 μm). Compared to single cells, palmelloids of C. priscuii showed a decrease in the abundance of light-harvesting complex II (LHCII) proteins with a 2-fold higher Chl a/b ratio. A decrease in both lutein and β-carotene in palmelloids resulted in carotenoid pools which were 27% lower in palmelloids compared to single cells of the psychrophile. Chlorophyll fluorescence analyses of the isolated fractions revealed that maximum photochemical efficiency of PSII (F(v)/F(m)) was comparable for both single cells and palmelloids of C. priscuii. However, isolated palmelloids exhibited lower excitation pressure, measured as 1 - qL, but higher yield of PSII (Φ(PSII)) and 50% higher rates of electron transport (ETR) than single cells exposed to high light at 8°C. This decreased sensitivity to high light in isolated palmelloids compared to single cells was associated with greater non-regulated dissipation of excess absorbed energy (Φ(NO)) with minimal differences in Φ(NPQ) in C. priscuii in response to increasing irradiance at low temperature. The ratio Φ(NO)/Φ(NPQ) observed for isolated palmelloids of C. priscuii developed at 8°C (1.414 ± 0.036) was 1.38-fold higher than Φ(NO)/Φ(NPQ) of isolated single cells (1.021 ± 0.018) exposed to low temperature combined with high light (1,000 μmol m(−2) s(−1)). The differences in the energy quenching capacities between palmelloids and single cells are discussed in terms of enhanced photoprotection of C. priscuii palmelloids against low-temperature photoinhibition. Frontiers Media S.A. 2022-08-31 /pmc/articles/PMC9470844/ /pubmed/36119589 http://dx.doi.org/10.3389/fpls.2022.911035 Text en Copyright © 2022 Szyszka-Mroz, Ivanov, Trick and Hüner. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Szyszka-Mroz, Beth
Ivanov, Alexander G.
Trick, Charles G.
Hüner, Norman P. A.
Palmelloid formation in the Antarctic psychrophile, Chlamydomonas priscuii, is photoprotective
title Palmelloid formation in the Antarctic psychrophile, Chlamydomonas priscuii, is photoprotective
title_full Palmelloid formation in the Antarctic psychrophile, Chlamydomonas priscuii, is photoprotective
title_fullStr Palmelloid formation in the Antarctic psychrophile, Chlamydomonas priscuii, is photoprotective
title_full_unstemmed Palmelloid formation in the Antarctic psychrophile, Chlamydomonas priscuii, is photoprotective
title_short Palmelloid formation in the Antarctic psychrophile, Chlamydomonas priscuii, is photoprotective
title_sort palmelloid formation in the antarctic psychrophile, chlamydomonas priscuii, is photoprotective
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9470844/
https://www.ncbi.nlm.nih.gov/pubmed/36119589
http://dx.doi.org/10.3389/fpls.2022.911035
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