Cargando…

Temporal system-level organization of the switch from glycolytic to gluconeogenic operation in yeast

The diauxic shift in Saccharomyces cerevisiae is an ideal model to study how eukaryotic cells readjust their metabolism from glycolytic to gluconeogenic operation. In this work, we generated time-resolved physiological data, quantitative metabolome (69 intracellular metabolites) and proteome (72 enz...

Descripción completa

Detalles Bibliográficos
Autores principales: Zampar, Guillermo G, Kümmel, Anne, Ewald, Jennifer, Jol, Stefan, Niebel, Bastian, Picotti, Paola, Aebersold, Ruedi, Sauer, Uwe, Zamboni, Nicola, Heinemann, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Molecular Biology Organization 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693829/
https://www.ncbi.nlm.nih.gov/pubmed/23549479
http://dx.doi.org/10.1038/msb.2013.11
_version_ 1782274756377051136
author Zampar, Guillermo G
Kümmel, Anne
Ewald, Jennifer
Jol, Stefan
Niebel, Bastian
Picotti, Paola
Aebersold, Ruedi
Sauer, Uwe
Zamboni, Nicola
Heinemann, Matthias
author_facet Zampar, Guillermo G
Kümmel, Anne
Ewald, Jennifer
Jol, Stefan
Niebel, Bastian
Picotti, Paola
Aebersold, Ruedi
Sauer, Uwe
Zamboni, Nicola
Heinemann, Matthias
author_sort Zampar, Guillermo G
collection PubMed
description The diauxic shift in Saccharomyces cerevisiae is an ideal model to study how eukaryotic cells readjust their metabolism from glycolytic to gluconeogenic operation. In this work, we generated time-resolved physiological data, quantitative metabolome (69 intracellular metabolites) and proteome (72 enzymes) profiles. We found that the diauxic shift is accomplished by three key events that are temporally organized: (i) a reduction in the glycolytic flux and the production of storage compounds before glucose depletion, mediated by downregulation of phosphofructokinase and pyruvate kinase reactions; (ii) upon glucose exhaustion, the reversion of carbon flow through glycolysis and onset of the glyoxylate cycle operation triggered by an increased expression of the enzymes that catalyze the malate synthase and cytosolic citrate synthase reactions; and (iii) in the later stages of the adaptation, the shutting down of the pentose phosphate pathway with a change in NADPH regeneration. Moreover, we identified the transcription factors associated with the observed changes in protein abundances. Taken together, our results represent an important contribution toward a systems-level understanding of how this adaptation is realized.
format Online
Article
Text
id pubmed-3693829
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher European Molecular Biology Organization
record_format MEDLINE/PubMed
spelling pubmed-36938292013-06-27 Temporal system-level organization of the switch from glycolytic to gluconeogenic operation in yeast Zampar, Guillermo G Kümmel, Anne Ewald, Jennifer Jol, Stefan Niebel, Bastian Picotti, Paola Aebersold, Ruedi Sauer, Uwe Zamboni, Nicola Heinemann, Matthias Mol Syst Biol Article The diauxic shift in Saccharomyces cerevisiae is an ideal model to study how eukaryotic cells readjust their metabolism from glycolytic to gluconeogenic operation. In this work, we generated time-resolved physiological data, quantitative metabolome (69 intracellular metabolites) and proteome (72 enzymes) profiles. We found that the diauxic shift is accomplished by three key events that are temporally organized: (i) a reduction in the glycolytic flux and the production of storage compounds before glucose depletion, mediated by downregulation of phosphofructokinase and pyruvate kinase reactions; (ii) upon glucose exhaustion, the reversion of carbon flow through glycolysis and onset of the glyoxylate cycle operation triggered by an increased expression of the enzymes that catalyze the malate synthase and cytosolic citrate synthase reactions; and (iii) in the later stages of the adaptation, the shutting down of the pentose phosphate pathway with a change in NADPH regeneration. Moreover, we identified the transcription factors associated with the observed changes in protein abundances. Taken together, our results represent an important contribution toward a systems-level understanding of how this adaptation is realized. European Molecular Biology Organization 2013-04-02 /pmc/articles/PMC3693829/ /pubmed/23549479 http://dx.doi.org/10.1038/msb.2013.11 Text en Copyright © 2013, EMBO and Macmillan Publishers Limited https://creativecommons.org/licenses/by/3.0/This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Article
Zampar, Guillermo G
Kümmel, Anne
Ewald, Jennifer
Jol, Stefan
Niebel, Bastian
Picotti, Paola
Aebersold, Ruedi
Sauer, Uwe
Zamboni, Nicola
Heinemann, Matthias
Temporal system-level organization of the switch from glycolytic to gluconeogenic operation in yeast
title Temporal system-level organization of the switch from glycolytic to gluconeogenic operation in yeast
title_full Temporal system-level organization of the switch from glycolytic to gluconeogenic operation in yeast
title_fullStr Temporal system-level organization of the switch from glycolytic to gluconeogenic operation in yeast
title_full_unstemmed Temporal system-level organization of the switch from glycolytic to gluconeogenic operation in yeast
title_short Temporal system-level organization of the switch from glycolytic to gluconeogenic operation in yeast
title_sort temporal system-level organization of the switch from glycolytic to gluconeogenic operation in yeast
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693829/
https://www.ncbi.nlm.nih.gov/pubmed/23549479
http://dx.doi.org/10.1038/msb.2013.11
work_keys_str_mv AT zamparguillermog temporalsystemlevelorganizationoftheswitchfromglycolytictogluconeogenicoperationinyeast
AT kummelanne temporalsystemlevelorganizationoftheswitchfromglycolytictogluconeogenicoperationinyeast
AT ewaldjennifer temporalsystemlevelorganizationoftheswitchfromglycolytictogluconeogenicoperationinyeast
AT jolstefan temporalsystemlevelorganizationoftheswitchfromglycolytictogluconeogenicoperationinyeast
AT niebelbastian temporalsystemlevelorganizationoftheswitchfromglycolytictogluconeogenicoperationinyeast
AT picottipaola temporalsystemlevelorganizationoftheswitchfromglycolytictogluconeogenicoperationinyeast
AT aebersoldruedi temporalsystemlevelorganizationoftheswitchfromglycolytictogluconeogenicoperationinyeast
AT saueruwe temporalsystemlevelorganizationoftheswitchfromglycolytictogluconeogenicoperationinyeast
AT zamboninicola temporalsystemlevelorganizationoftheswitchfromglycolytictogluconeogenicoperationinyeast
AT heinemannmatthias temporalsystemlevelorganizationoftheswitchfromglycolytictogluconeogenicoperationinyeast