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Temperature sensitivity of carbon concentrating mechanisms in the diatom Phaeodactylum tricornutum

Marine diatoms are key primary producers across diverse habitats in the global ocean. Diatoms rely on a biophysical carbon concentrating mechanism (CCM) to supply high concentrations of CO(2) around their carboxylating enzyme, RuBisCO. The necessity and energetic cost of the CCM are likely to be hig...

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Autores principales: Li, Meng, Young, Jodi N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154264/
https://www.ncbi.nlm.nih.gov/pubmed/36881356
http://dx.doi.org/10.1007/s11120-023-01004-2
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author Li, Meng
Young, Jodi N.
author_facet Li, Meng
Young, Jodi N.
author_sort Li, Meng
collection PubMed
description Marine diatoms are key primary producers across diverse habitats in the global ocean. Diatoms rely on a biophysical carbon concentrating mechanism (CCM) to supply high concentrations of CO(2) around their carboxylating enzyme, RuBisCO. The necessity and energetic cost of the CCM are likely to be highly sensitive to temperature, as temperature impacts CO(2) concentration, diffusivity, and the kinetics of CCM components. Here, we used membrane inlet mass spectrometry (MIMS) and modeling to capture temperature regulation of the CCM in the diatom Phaeodactylum tricornutum (Pt). We found that enhanced carbon fixation rates by Pt at elevated temperatures were accompanied by increased CCM activity capable of maintaining RuBisCO close to CO(2) saturation but that the mechanism varied. At 10 and 18 °C, diffusion of CO(2) into the cell, driven by Pt’s ‘chloroplast pump’ was the major inorganic carbon source. However, at 18 °C, upregulation of the chloroplast pump enhanced (while retaining the proportion of) both diffusive CO(2) and active HCO(3)(−) uptake into the cytosol, and significantly increased chloroplast HCO(3)(−) concentrations. In contrast, at 25 °C, compared to 18 °C, the chloroplast pump had only a slight increase in activity. While diffusive uptake of CO(2) into the cell remained constant, active HCO(3)(−) uptake across the cell membrane increased resulting in Pt depending equally on both CO(2) and HCO(3)(−) as inorganic carbon sources. Despite changes in the CCM, the overall rate of active carbon transport remained double that of carbon fixation across all temperatures tested. The implication of the energetic cost of the Pt CCM in response to increasing temperatures was discussed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11120-023-01004-2.
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spelling pubmed-101542642023-05-04 Temperature sensitivity of carbon concentrating mechanisms in the diatom Phaeodactylum tricornutum Li, Meng Young, Jodi N. Photosynth Res Research Marine diatoms are key primary producers across diverse habitats in the global ocean. Diatoms rely on a biophysical carbon concentrating mechanism (CCM) to supply high concentrations of CO(2) around their carboxylating enzyme, RuBisCO. The necessity and energetic cost of the CCM are likely to be highly sensitive to temperature, as temperature impacts CO(2) concentration, diffusivity, and the kinetics of CCM components. Here, we used membrane inlet mass spectrometry (MIMS) and modeling to capture temperature regulation of the CCM in the diatom Phaeodactylum tricornutum (Pt). We found that enhanced carbon fixation rates by Pt at elevated temperatures were accompanied by increased CCM activity capable of maintaining RuBisCO close to CO(2) saturation but that the mechanism varied. At 10 and 18 °C, diffusion of CO(2) into the cell, driven by Pt’s ‘chloroplast pump’ was the major inorganic carbon source. However, at 18 °C, upregulation of the chloroplast pump enhanced (while retaining the proportion of) both diffusive CO(2) and active HCO(3)(−) uptake into the cytosol, and significantly increased chloroplast HCO(3)(−) concentrations. In contrast, at 25 °C, compared to 18 °C, the chloroplast pump had only a slight increase in activity. While diffusive uptake of CO(2) into the cell remained constant, active HCO(3)(−) uptake across the cell membrane increased resulting in Pt depending equally on both CO(2) and HCO(3)(−) as inorganic carbon sources. Despite changes in the CCM, the overall rate of active carbon transport remained double that of carbon fixation across all temperatures tested. The implication of the energetic cost of the Pt CCM in response to increasing temperatures was discussed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11120-023-01004-2. Springer Netherlands 2023-03-07 2023 /pmc/articles/PMC10154264/ /pubmed/36881356 http://dx.doi.org/10.1007/s11120-023-01004-2 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Li, Meng
Young, Jodi N.
Temperature sensitivity of carbon concentrating mechanisms in the diatom Phaeodactylum tricornutum
title Temperature sensitivity of carbon concentrating mechanisms in the diatom Phaeodactylum tricornutum
title_full Temperature sensitivity of carbon concentrating mechanisms in the diatom Phaeodactylum tricornutum
title_fullStr Temperature sensitivity of carbon concentrating mechanisms in the diatom Phaeodactylum tricornutum
title_full_unstemmed Temperature sensitivity of carbon concentrating mechanisms in the diatom Phaeodactylum tricornutum
title_short Temperature sensitivity of carbon concentrating mechanisms in the diatom Phaeodactylum tricornutum
title_sort temperature sensitivity of carbon concentrating mechanisms in the diatom phaeodactylum tricornutum
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154264/
https://www.ncbi.nlm.nih.gov/pubmed/36881356
http://dx.doi.org/10.1007/s11120-023-01004-2
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