Grant: Discovery Grants Program - Individual
University of Guelph
$21,500.00
Adaptive response of saccharomyces cerevisiae to fermentation-related stresses
EF 2007-08
Résumé
The yeast Saccharomyces cerevisiae have two very important functions: it serves as an eukaryotic model organism in which fundamental processes of eukaryotic cell biology, molecular biology and metabolism can be studied, and it has enormous industrial relevance as it serves to produce bread, wine, beer and bio-ethanol. During beverage and bio-ethanol production the yeast is used to ferment high concentrations of fermentable sugars into ethanol and carbon dioxide. These production processes present the yeast with a variety of stresses that ultimately influences its ability to perform fermentations efficiently. Fermentation stresses include an initial high sugar content (osmotic stress), and increasing ethanol production and nutrietn (carbon and nitrogen) depletion as the fermentation proceeds. Understanding the mechanisms that enable yeast to cope with these stresses will allow us to develop yeast strains that are more efficient during the fermentation process. Effective fermentations are largely determined by the yeast's ability to take up and ferment glucose and fructose. A family of hexose transporters (Hxt1-17) that range in their affinities for glucose or fructose are used by the yeast to take up fermentable carbon sources and its tolerance to ethanol. The most important transporters during wine (batch) fermentations have are Hxt1, Hxt3, Hxt5, Hxt6 and Hxt7.We have shown that a family of yeast genes, the GID/VID genes, are needed by the yeast to respond effectively to nutrient depletion, osmotic stress and, surprisingly, influence the yeast's ability to take up glucose and to produce ethanol. The Gid/Vid proteins form a complex, the Gid Protein Complex (GPC), which are responsible for the regulated proteolysis of FBPase when carbon-starved cells are replenished with glucose. We have shown that components of the GPC are needed for the regulated degradation of Hxt7 in response to changing nutrient conditions. However, the mechanism(s) of function of the GPC or its individual components, are poorly understood. This proposal is aimed at increasing our understanding of the GPC and, specifically, four of its components.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
262276-2007
Name nom
VanDerMerwe, George
Department département
Molecular and Cellular Biology
Organization id
24
Institution établissement
University of Guelph
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2007
Competition year année de concours
2007
Award amount
21500
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
33
Committee name en
Molec. & Develop. Genetics
Committee name fr
Gén. moléculaire et dévelop.
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
5200
Research subject group en
Microbiology
Research subject group fr
Microbiologie
Research subject en
Microbiology
Research subject fr
Microbiologie
Partie
1
Nb partie
1
Application title
Adaptive response of saccharomyces cerevisiae to fermentation-related stresses
Keyword
NA
Application summary
The yeast Saccharomyces cerevisiae have two very important functions: it serves as an eukaryotic model organism in which fundamental processes of eukaryotic cell biology, molecular biology and metabolism can be studied, and it has enormous industrial relevance as it serves to produce bread, wine, beer and bio-ethanol. During beverage and bio-ethanol production the yeast is used to ferment high concentrations of fermentable sugars into ethanol and carbon dioxide. These production processes present the yeast with a variety of stresses that ultimately influences its ability to perform fermentations efficiently. Fermentation stresses include an initial high sugar content (osmotic stress), and increasing ethanol production and nutrietn (carbon and nitrogen) depletion as the fermentation proceeds. Understanding the mechanisms that enable yeast to cope with these stresses will allow us to develop yeast strains that are more efficient during the fermentation process. Effective fermentations are largely determined by the yeast's ability to take up and ferment glucose and fructose. A family of hexose transporters (Hxt1-17) that range in their affinities for glucose or fructose are used by the yeast to take up fermentable carbon sources and its tolerance to ethanol. The most important transporters during wine (batch) fermentations have are Hxt1, Hxt3, Hxt5, Hxt6 and Hxt7.We have shown that a family of yeast genes, the GID/VID genes, are needed by the yeast to respond effectively to nutrient depletion, osmotic stress and, surprisingly, influence the yeast's ability to take up glucose and to produce ethanol. The Gid/Vid proteins form a complex, the Gid Protein Complex (GPC), which are responsible for the regulated proteolysis of FBPase when carbon-starved cells are replenished with glucose. We have shown that components of the GPC are needed for the regulated degradation of Hxt7 in response to changing nutrient conditions. However, the mechanism(s) of function of the GPC or its individual components, are poorly understood. This proposal is aimed at increasing our understanding of the GPC and, specifically, four of its components.