Cargando…

The Transition Toward Nitrogen Deprivation in Diatoms Requires Chloroplast Stand-By and Deep Metabolic Reshuffling

Microalgae have adapted to face abiotic stresses by accumulating energy storage molecules such as lipids, which are also of interest to industries. Unfortunately, the impairment in cell division during the accumulation of these molecules constitutes a major bottleneck for the development of efficien...

Descripción completa

Detalles Bibliográficos
Autores principales: Scarsini, Matteo, Thiriet-Rupert, Stanislas, Veidl, Brigitte, Mondeguer, Florence, Hu, Hanhua, Marchand, Justine, Schoefs, Benoît
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8811913/
https://www.ncbi.nlm.nih.gov/pubmed/35126407
http://dx.doi.org/10.3389/fpls.2021.760516
_version_ 1784644533739323392
author Scarsini, Matteo
Thiriet-Rupert, Stanislas
Veidl, Brigitte
Mondeguer, Florence
Hu, Hanhua
Marchand, Justine
Schoefs, Benoît
author_facet Scarsini, Matteo
Thiriet-Rupert, Stanislas
Veidl, Brigitte
Mondeguer, Florence
Hu, Hanhua
Marchand, Justine
Schoefs, Benoît
author_sort Scarsini, Matteo
collection PubMed
description Microalgae have adapted to face abiotic stresses by accumulating energy storage molecules such as lipids, which are also of interest to industries. Unfortunately, the impairment in cell division during the accumulation of these molecules constitutes a major bottleneck for the development of efficient microalgae-based biotechnology processes. To address the bottleneck, a multidisciplinary approach was used to study the mechanisms involved in the transition from nitrogen repletion to nitrogen starvation conditions in the marine diatom Phaeodactylum tricornutum that was cultured in a turbidostat. Combining data demonstrate that the different steps of nitrogen deficiency clustered together in a single state in which cells are in equilibrium with their environment. The switch between the nitrogen-replete and the nitrogen-deficient equilibrium is driven by intracellular nitrogen availability. The switch induces a major gene expression change, which is reflected in the reorientation of the carbon metabolism toward an energy storage mode while still operating as a metabolic flywheel. Although the photosynthetic activity is reduced, the chloroplast is kept in a stand-by mode allowing a fast resuming upon nitrogen repletion. Altogether, these results contribute to the understanding of the intricate response of diatoms under stress.
format Online
Article
Text
id pubmed-8811913
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-88119132022-02-04 The Transition Toward Nitrogen Deprivation in Diatoms Requires Chloroplast Stand-By and Deep Metabolic Reshuffling Scarsini, Matteo Thiriet-Rupert, Stanislas Veidl, Brigitte Mondeguer, Florence Hu, Hanhua Marchand, Justine Schoefs, Benoît Front Plant Sci Plant Science Microalgae have adapted to face abiotic stresses by accumulating energy storage molecules such as lipids, which are also of interest to industries. Unfortunately, the impairment in cell division during the accumulation of these molecules constitutes a major bottleneck for the development of efficient microalgae-based biotechnology processes. To address the bottleneck, a multidisciplinary approach was used to study the mechanisms involved in the transition from nitrogen repletion to nitrogen starvation conditions in the marine diatom Phaeodactylum tricornutum that was cultured in a turbidostat. Combining data demonstrate that the different steps of nitrogen deficiency clustered together in a single state in which cells are in equilibrium with their environment. The switch between the nitrogen-replete and the nitrogen-deficient equilibrium is driven by intracellular nitrogen availability. The switch induces a major gene expression change, which is reflected in the reorientation of the carbon metabolism toward an energy storage mode while still operating as a metabolic flywheel. Although the photosynthetic activity is reduced, the chloroplast is kept in a stand-by mode allowing a fast resuming upon nitrogen repletion. Altogether, these results contribute to the understanding of the intricate response of diatoms under stress. Frontiers Media S.A. 2022-01-18 /pmc/articles/PMC8811913/ /pubmed/35126407 http://dx.doi.org/10.3389/fpls.2021.760516 Text en Copyright © 2022 Scarsini, Thiriet-Rupert, Veidl, Mondeguer, Hu, Marchand and Schoefs. 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
Scarsini, Matteo
Thiriet-Rupert, Stanislas
Veidl, Brigitte
Mondeguer, Florence
Hu, Hanhua
Marchand, Justine
Schoefs, Benoît
The Transition Toward Nitrogen Deprivation in Diatoms Requires Chloroplast Stand-By and Deep Metabolic Reshuffling
title The Transition Toward Nitrogen Deprivation in Diatoms Requires Chloroplast Stand-By and Deep Metabolic Reshuffling
title_full The Transition Toward Nitrogen Deprivation in Diatoms Requires Chloroplast Stand-By and Deep Metabolic Reshuffling
title_fullStr The Transition Toward Nitrogen Deprivation in Diatoms Requires Chloroplast Stand-By and Deep Metabolic Reshuffling
title_full_unstemmed The Transition Toward Nitrogen Deprivation in Diatoms Requires Chloroplast Stand-By and Deep Metabolic Reshuffling
title_short The Transition Toward Nitrogen Deprivation in Diatoms Requires Chloroplast Stand-By and Deep Metabolic Reshuffling
title_sort transition toward nitrogen deprivation in diatoms requires chloroplast stand-by and deep metabolic reshuffling
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8811913/
https://www.ncbi.nlm.nih.gov/pubmed/35126407
http://dx.doi.org/10.3389/fpls.2021.760516
work_keys_str_mv AT scarsinimatteo thetransitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT thirietrupertstanislas thetransitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT veidlbrigitte thetransitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT mondeguerflorence thetransitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT huhanhua thetransitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT marchandjustine thetransitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT schoefsbenoit thetransitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT scarsinimatteo transitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT thirietrupertstanislas transitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT veidlbrigitte transitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT mondeguerflorence transitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT huhanhua transitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT marchandjustine transitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling
AT schoefsbenoit transitiontowardnitrogendeprivationindiatomsrequireschloroplaststandbyanddeepmetabolicreshuffling