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Fatal attraction in glycolysis: how Saccharomyces cerevisiae manages sudden transitions to high glucose
In the model eukaryote Saccharomyces cerevisiae, it has long been known that a functional trehalose pathway is indispensable for transitions to high glucose conditions. Upon addition of glucose, cells with a defect in trehalose 6-phosphate synthase (Tps1), the first committed step in the trehalose p...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shared Science Publishers OG
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349229/ https://www.ncbi.nlm.nih.gov/pubmed/28357229 http://dx.doi.org/10.15698/mic2014.01.133 |
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author | Heerden, Johan H. v. Wortel, Meike T. Bruggeman, Frank J. Heijnen, Joseph J. Bollen, Yves J. Planqué, Robert Hulshof, Josephus O’Toole, Tom G. Wahl, S. A. Teusink, Bas |
author_facet | Heerden, Johan H. v. Wortel, Meike T. Bruggeman, Frank J. Heijnen, Joseph J. Bollen, Yves J. Planqué, Robert Hulshof, Josephus O’Toole, Tom G. Wahl, S. A. Teusink, Bas |
author_sort | Heerden, Johan H. v. |
collection | PubMed |
description | In the model eukaryote Saccharomyces cerevisiae, it has long been known that a functional trehalose pathway is indispensable for transitions to high glucose conditions. Upon addition of glucose, cells with a defect in trehalose 6-phosphate synthase (Tps1), the first committed step in the trehalose pathway, display what we have termed an imbalanced glycolytic state; in this state the flux through the upper part of glycolysis outpaces that through the lower part of glycolysis. As a consequence, the intermediate fructose 1,6-bisphosphate (FBP) accumulates at low concentrations of ATP and inorganic phosphate (P(i)). Despite significant research efforts, a satisfactory understanding of the regulatory role that trehalose metabolism plays during such transitions has remained infamously unresolved. In a recent study, we demonstrate that the startup of glycolysis exhibits two dynamic fates: a proper, functional, steady state or the imbalanced state described above. Both states are stable, attracting states, and the probability distribution of initial states determines the fate of a yeast cell exposed to glucose. Trehalose metabolism steers the dynamics of glycolysis towards the proper functional state through its ATP hydrolysis activity; a mechanism that ensures that the demand and supply of ATP is balanced with P(i) availability under dynamic conditions. [van Heerden et al. Science (2014), DOI: 10.1126/science.1245114.] |
format | Online Article Text |
id | pubmed-5349229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Shared Science Publishers OG |
record_format | MEDLINE/PubMed |
spelling | pubmed-53492292017-03-29 Fatal attraction in glycolysis: how Saccharomyces cerevisiae manages sudden transitions to high glucose Heerden, Johan H. v. Wortel, Meike T. Bruggeman, Frank J. Heijnen, Joseph J. Bollen, Yves J. Planqué, Robert Hulshof, Josephus O’Toole, Tom G. Wahl, S. A. Teusink, Bas Microb Cell Microbiology In the model eukaryote Saccharomyces cerevisiae, it has long been known that a functional trehalose pathway is indispensable for transitions to high glucose conditions. Upon addition of glucose, cells with a defect in trehalose 6-phosphate synthase (Tps1), the first committed step in the trehalose pathway, display what we have termed an imbalanced glycolytic state; in this state the flux through the upper part of glycolysis outpaces that through the lower part of glycolysis. As a consequence, the intermediate fructose 1,6-bisphosphate (FBP) accumulates at low concentrations of ATP and inorganic phosphate (P(i)). Despite significant research efforts, a satisfactory understanding of the regulatory role that trehalose metabolism plays during such transitions has remained infamously unresolved. In a recent study, we demonstrate that the startup of glycolysis exhibits two dynamic fates: a proper, functional, steady state or the imbalanced state described above. Both states are stable, attracting states, and the probability distribution of initial states determines the fate of a yeast cell exposed to glucose. Trehalose metabolism steers the dynamics of glycolysis towards the proper functional state through its ATP hydrolysis activity; a mechanism that ensures that the demand and supply of ATP is balanced with P(i) availability under dynamic conditions. [van Heerden et al. Science (2014), DOI: 10.1126/science.1245114.] Shared Science Publishers OG 2014-02-20 /pmc/articles/PMC5349229/ /pubmed/28357229 http://dx.doi.org/10.15698/mic2014.01.133 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged. |
spellingShingle | Microbiology Heerden, Johan H. v. Wortel, Meike T. Bruggeman, Frank J. Heijnen, Joseph J. Bollen, Yves J. Planqué, Robert Hulshof, Josephus O’Toole, Tom G. Wahl, S. A. Teusink, Bas Fatal attraction in glycolysis: how Saccharomyces cerevisiae manages sudden transitions to high glucose |
title | Fatal attraction in glycolysis: how Saccharomyces cerevisiae manages sudden transitions to high glucose |
title_full | Fatal attraction in glycolysis: how Saccharomyces cerevisiae manages sudden transitions to high glucose |
title_fullStr | Fatal attraction in glycolysis: how Saccharomyces cerevisiae manages sudden transitions to high glucose |
title_full_unstemmed | Fatal attraction in glycolysis: how Saccharomyces cerevisiae manages sudden transitions to high glucose |
title_short | Fatal attraction in glycolysis: how Saccharomyces cerevisiae manages sudden transitions to high glucose |
title_sort | fatal attraction in glycolysis: how saccharomyces cerevisiae manages sudden transitions to high glucose |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349229/ https://www.ncbi.nlm.nih.gov/pubmed/28357229 http://dx.doi.org/10.15698/mic2014.01.133 |
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