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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2014
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
Descripción
Sumario: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.]