Cargando…
CO(2) supply modulates lipid remodelling, photosynthetic and respiratory activities in Chlorella species
Microalgae represent a potential solution to reduce CO(2) emission exploiting their photosynthetic activity. Here, the physiologic and metabolic responses at the base of CO(2) assimilation were investigated in conditions of high or low CO(2) availability in two of the most promising algae species fo...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453743/ https://www.ncbi.nlm.nih.gov/pubmed/33931891 http://dx.doi.org/10.1111/pce.14074 |
_version_ | 1784570335975178240 |
---|---|
author | Cecchin, Michela Paloschi, Matteo Busnardo, Giovanni Cazzaniga, Stefano Cuine, Stephan Li‐Beisson, Yonghua Wobbe, Lutz Ballottari, Matteo |
author_facet | Cecchin, Michela Paloschi, Matteo Busnardo, Giovanni Cazzaniga, Stefano Cuine, Stephan Li‐Beisson, Yonghua Wobbe, Lutz Ballottari, Matteo |
author_sort | Cecchin, Michela |
collection | PubMed |
description | Microalgae represent a potential solution to reduce CO(2) emission exploiting their photosynthetic activity. Here, the physiologic and metabolic responses at the base of CO(2) assimilation were investigated in conditions of high or low CO(2) availability in two of the most promising algae species for industrial cultivation, Chlorella sorokiniana and Chlorella vulgaris. In both species, high CO(2) availability increased biomass accumulation with specific increase of triacylglycerols in C. vulgaris and polar lipids and proteins in C. sorokiniana. Moreover, high CO(2) availability caused only in C. vulgaris a reduced NAD(P)H/NADP(+) ratio and reduced mitochondrial respiration, suggesting a CO(2) dependent increase of reducing power consumption in the chloroplast, which in turn influences the redox state of the mitochondria. Several rearrangements of the photosynthetic machinery were observed in both species, differing from those described for the model organism Chlamydomonas reinhardtii, where adaptation to carbon availability is mainly controlled by the translational repressor NAB1. NAB1 homologous protein could be identified only in C. vulgaris but lacked the regulation mechanisms previously described in C. reinhardtii. Acclimation strategies to cope with a fluctuating inorganic carbon supply are thus diverse among green microalgae, and these results suggest new biotechnological strategies to boost CO(2) fixation. |
format | Online Article Text |
id | pubmed-8453743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84537432021-09-27 CO(2) supply modulates lipid remodelling, photosynthetic and respiratory activities in Chlorella species Cecchin, Michela Paloschi, Matteo Busnardo, Giovanni Cazzaniga, Stefano Cuine, Stephan Li‐Beisson, Yonghua Wobbe, Lutz Ballottari, Matteo Plant Cell Environ Original Articles Microalgae represent a potential solution to reduce CO(2) emission exploiting their photosynthetic activity. Here, the physiologic and metabolic responses at the base of CO(2) assimilation were investigated in conditions of high or low CO(2) availability in two of the most promising algae species for industrial cultivation, Chlorella sorokiniana and Chlorella vulgaris. In both species, high CO(2) availability increased biomass accumulation with specific increase of triacylglycerols in C. vulgaris and polar lipids and proteins in C. sorokiniana. Moreover, high CO(2) availability caused only in C. vulgaris a reduced NAD(P)H/NADP(+) ratio and reduced mitochondrial respiration, suggesting a CO(2) dependent increase of reducing power consumption in the chloroplast, which in turn influences the redox state of the mitochondria. Several rearrangements of the photosynthetic machinery were observed in both species, differing from those described for the model organism Chlamydomonas reinhardtii, where adaptation to carbon availability is mainly controlled by the translational repressor NAB1. NAB1 homologous protein could be identified only in C. vulgaris but lacked the regulation mechanisms previously described in C. reinhardtii. Acclimation strategies to cope with a fluctuating inorganic carbon supply are thus diverse among green microalgae, and these results suggest new biotechnological strategies to boost CO(2) fixation. John Wiley & Sons, Ltd. 2021-05-17 2021-09 /pmc/articles/PMC8453743/ /pubmed/33931891 http://dx.doi.org/10.1111/pce.14074 Text en © 2021 The Authors. Plant, Cell & Environment published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Cecchin, Michela Paloschi, Matteo Busnardo, Giovanni Cazzaniga, Stefano Cuine, Stephan Li‐Beisson, Yonghua Wobbe, Lutz Ballottari, Matteo CO(2) supply modulates lipid remodelling, photosynthetic and respiratory activities in Chlorella species |
title | CO(2)
supply modulates lipid remodelling, photosynthetic and respiratory activities in Chlorella species |
title_full | CO(2)
supply modulates lipid remodelling, photosynthetic and respiratory activities in Chlorella species |
title_fullStr | CO(2)
supply modulates lipid remodelling, photosynthetic and respiratory activities in Chlorella species |
title_full_unstemmed | CO(2)
supply modulates lipid remodelling, photosynthetic and respiratory activities in Chlorella species |
title_short | CO(2)
supply modulates lipid remodelling, photosynthetic and respiratory activities in Chlorella species |
title_sort | co(2)
supply modulates lipid remodelling, photosynthetic and respiratory activities in chlorella species |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453743/ https://www.ncbi.nlm.nih.gov/pubmed/33931891 http://dx.doi.org/10.1111/pce.14074 |
work_keys_str_mv | AT cecchinmichela co2supplymodulateslipidremodellingphotosyntheticandrespiratoryactivitiesinchlorellaspecies AT paloschimatteo co2supplymodulateslipidremodellingphotosyntheticandrespiratoryactivitiesinchlorellaspecies AT busnardogiovanni co2supplymodulateslipidremodellingphotosyntheticandrespiratoryactivitiesinchlorellaspecies AT cazzanigastefano co2supplymodulateslipidremodellingphotosyntheticandrespiratoryactivitiesinchlorellaspecies AT cuinestephan co2supplymodulateslipidremodellingphotosyntheticandrespiratoryactivitiesinchlorellaspecies AT libeissonyonghua co2supplymodulateslipidremodellingphotosyntheticandrespiratoryactivitiesinchlorellaspecies AT wobbelutz co2supplymodulateslipidremodellingphotosyntheticandrespiratoryactivitiesinchlorellaspecies AT ballottarimatteo co2supplymodulateslipidremodellingphotosyntheticandrespiratoryactivitiesinchlorellaspecies |