Cargando…

Cytochrome c Deficiency Differentially Affects the In Vivo Mitochondrial Electron Partitioning and Primary Metabolism Depending on the Photoperiod

Plant respiration provides metabolic flexibility under changing environmental conditions by modulating the activity of the nonphosphorylating alternative pathways from the mitochondrial electron transport chain, which bypass the main energy-producing components of the cytochrome oxidase pathway (COP...

Descripción completa

Detalles Bibliográficos
Autores principales: Florez-Sarasa, Igor, Welchen, Elina, Racca, Sofia, Gonzalez, Daniel H., Vallarino, José G., Fernie, Alisdair R., Ribas-Carbo, Miquel, Del-Saz, Nestor Fernandez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7996904/
https://www.ncbi.nlm.nih.gov/pubmed/33652808
http://dx.doi.org/10.3390/plants10030444
_version_ 1783670207052513280
author Florez-Sarasa, Igor
Welchen, Elina
Racca, Sofia
Gonzalez, Daniel H.
Vallarino, José G.
Fernie, Alisdair R.
Ribas-Carbo, Miquel
Del-Saz, Nestor Fernandez
author_facet Florez-Sarasa, Igor
Welchen, Elina
Racca, Sofia
Gonzalez, Daniel H.
Vallarino, José G.
Fernie, Alisdair R.
Ribas-Carbo, Miquel
Del-Saz, Nestor Fernandez
author_sort Florez-Sarasa, Igor
collection PubMed
description Plant respiration provides metabolic flexibility under changing environmental conditions by modulating the activity of the nonphosphorylating alternative pathways from the mitochondrial electron transport chain, which bypass the main energy-producing components of the cytochrome oxidase pathway (COP). While adjustments in leaf primary metabolism induced by changes in day length are well studied, possible differences in the in vivo contribution of the COP and the alternative oxidase pathway (AOP) between different photoperiods remain unknown. In our study, in vivo electron partitioning between AOP and COP and expression analysis of respiratory components, photosynthesis, and the levels of primary metabolites were studied in leaves of wild-type (WT) plants and cytochrome c (CYTc) mutants, with reduced levels of COP components, under short- and long-day photoperiods. Our results clearly show that differences in AOP and COP in vivo activities between WT and cytc mutants depend on the photoperiod likely due to energy and stress signaling constraints. Parallel responses observed between in vivo respiratory activities, TCA cycle intermediates, amino acids, and stress signaling metabolites indicate the coordination of different pathways of primary metabolism to support growth adaptation under different photoperiods.
format Online
Article
Text
id pubmed-7996904
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-79969042021-03-27 Cytochrome c Deficiency Differentially Affects the In Vivo Mitochondrial Electron Partitioning and Primary Metabolism Depending on the Photoperiod Florez-Sarasa, Igor Welchen, Elina Racca, Sofia Gonzalez, Daniel H. Vallarino, José G. Fernie, Alisdair R. Ribas-Carbo, Miquel Del-Saz, Nestor Fernandez Plants (Basel) Article Plant respiration provides metabolic flexibility under changing environmental conditions by modulating the activity of the nonphosphorylating alternative pathways from the mitochondrial electron transport chain, which bypass the main energy-producing components of the cytochrome oxidase pathway (COP). While adjustments in leaf primary metabolism induced by changes in day length are well studied, possible differences in the in vivo contribution of the COP and the alternative oxidase pathway (AOP) between different photoperiods remain unknown. In our study, in vivo electron partitioning between AOP and COP and expression analysis of respiratory components, photosynthesis, and the levels of primary metabolites were studied in leaves of wild-type (WT) plants and cytochrome c (CYTc) mutants, with reduced levels of COP components, under short- and long-day photoperiods. Our results clearly show that differences in AOP and COP in vivo activities between WT and cytc mutants depend on the photoperiod likely due to energy and stress signaling constraints. Parallel responses observed between in vivo respiratory activities, TCA cycle intermediates, amino acids, and stress signaling metabolites indicate the coordination of different pathways of primary metabolism to support growth adaptation under different photoperiods. MDPI 2021-02-26 /pmc/articles/PMC7996904/ /pubmed/33652808 http://dx.doi.org/10.3390/plants10030444 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Florez-Sarasa, Igor
Welchen, Elina
Racca, Sofia
Gonzalez, Daniel H.
Vallarino, José G.
Fernie, Alisdair R.
Ribas-Carbo, Miquel
Del-Saz, Nestor Fernandez
Cytochrome c Deficiency Differentially Affects the In Vivo Mitochondrial Electron Partitioning and Primary Metabolism Depending on the Photoperiod
title Cytochrome c Deficiency Differentially Affects the In Vivo Mitochondrial Electron Partitioning and Primary Metabolism Depending on the Photoperiod
title_full Cytochrome c Deficiency Differentially Affects the In Vivo Mitochondrial Electron Partitioning and Primary Metabolism Depending on the Photoperiod
title_fullStr Cytochrome c Deficiency Differentially Affects the In Vivo Mitochondrial Electron Partitioning and Primary Metabolism Depending on the Photoperiod
title_full_unstemmed Cytochrome c Deficiency Differentially Affects the In Vivo Mitochondrial Electron Partitioning and Primary Metabolism Depending on the Photoperiod
title_short Cytochrome c Deficiency Differentially Affects the In Vivo Mitochondrial Electron Partitioning and Primary Metabolism Depending on the Photoperiod
title_sort cytochrome c deficiency differentially affects the in vivo mitochondrial electron partitioning and primary metabolism depending on the photoperiod
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7996904/
https://www.ncbi.nlm.nih.gov/pubmed/33652808
http://dx.doi.org/10.3390/plants10030444
work_keys_str_mv AT florezsarasaigor cytochromecdeficiencydifferentiallyaffectstheinvivomitochondrialelectronpartitioningandprimarymetabolismdependingonthephotoperiod
AT welchenelina cytochromecdeficiencydifferentiallyaffectstheinvivomitochondrialelectronpartitioningandprimarymetabolismdependingonthephotoperiod
AT raccasofia cytochromecdeficiencydifferentiallyaffectstheinvivomitochondrialelectronpartitioningandprimarymetabolismdependingonthephotoperiod
AT gonzalezdanielh cytochromecdeficiencydifferentiallyaffectstheinvivomitochondrialelectronpartitioningandprimarymetabolismdependingonthephotoperiod
AT vallarinojoseg cytochromecdeficiencydifferentiallyaffectstheinvivomitochondrialelectronpartitioningandprimarymetabolismdependingonthephotoperiod
AT ferniealisdairr cytochromecdeficiencydifferentiallyaffectstheinvivomitochondrialelectronpartitioningandprimarymetabolismdependingonthephotoperiod
AT ribascarbomiquel cytochromecdeficiencydifferentiallyaffectstheinvivomitochondrialelectronpartitioningandprimarymetabolismdependingonthephotoperiod
AT delsaznestorfernandez cytochromecdeficiencydifferentiallyaffectstheinvivomitochondrialelectronpartitioningandprimarymetabolismdependingonthephotoperiod