Genome-wide expression analyses: Metabolic adaptation of Saccharomyces cerevisiae to high sugar stress

The transcriptional response of laboratory strains of Saccharomyces cerevisiae to salt or sorbitol stress has been well studied. These studies have yielded valuable data on how the yeast adapts to these stress conditions. However, S. cerevisiae is a saccharophilic fungus and in its natural environme...

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Veröffentlicht in:FEMS yeast research 2003-06, Vol.3 (4), p.375-399
Hauptverfasser: Erasmus, Daniel J, van der Merwe, George K, van Vuuren, Hennie J.J
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van Vuuren, Hennie J.J
description The transcriptional response of laboratory strains of Saccharomyces cerevisiae to salt or sorbitol stress has been well studied. These studies have yielded valuable data on how the yeast adapts to these stress conditions. However, S. cerevisiae is a saccharophilic fungus and in its natural environment this yeast encounters high concentrations of sugars. For the production of dessert wines, the sugar concentration may be as high as 50% (w/v). The metabolic pathways in S. cerevisiae under these fermentation conditions have not been studied and the transcriptional response of this yeast to sugar stress has not been investigated. High-density DNA microarrays showed that the transcription of 589 genes in an industrial strain of S. cerevisiae were affected more than two-fold in grape juice containing 40% (w/v) sugars (equimolar amounts of glucose and fructose). High sugar stress up-regulated the glycolytic and pentose phosphate pathway genes. The PDC6 gene, previously thought to encode a minor isozyme of pyruvate decarboxylase, was highly induced under these conditions. Gene expression profiles indicate that the oxidative and non-oxidative branches of the pentose phosphate pathway were up-regulated and might be used to shunt more glucose-6-phosphate and fructose-6-phosphate, respectively, from the glycolytic pathway into the pentose phosphate pathway. Structural genes involved in the formation of acetic acid from acetaldehyde, and succinic acid from glutamate, were also up-regulated. Genes involved in de novo biosynthesis of purines, pyrimidines, histidine and lysine were down-regulated by sugar stress.
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Gene expression profiles indicate that the oxidative and non-oxidative branches of the pentose phosphate pathway were up-regulated and might be used to shunt more glucose-6-phosphate and fructose-6-phosphate, respectively, from the glycolytic pathway into the pentose phosphate pathway. Structural genes involved in the formation of acetic acid from acetaldehyde, and succinic acid from glutamate, were also up-regulated. 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Gene expression profiles indicate that the oxidative and non-oxidative branches of the pentose phosphate pathway were up-regulated and might be used to shunt more glucose-6-phosphate and fructose-6-phosphate, respectively, from the glycolytic pathway into the pentose phosphate pathway. Structural genes involved in the formation of acetic acid from acetaldehyde, and succinic acid from glutamate, were also up-regulated. 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These studies have yielded valuable data on how the yeast adapts to these stress conditions. However, S. cerevisiae is a saccharophilic fungus and in its natural environment this yeast encounters high concentrations of sugars. For the production of dessert wines, the sugar concentration may be as high as 50% (w/v). The metabolic pathways in S. cerevisiae under these fermentation conditions have not been studied and the transcriptional response of this yeast to sugar stress has not been investigated. High-density DNA microarrays showed that the transcription of 589 genes in an industrial strain of S. cerevisiae were affected more than two-fold in grape juice containing 40% (w/v) sugars (equimolar amounts of glucose and fructose). High sugar stress up-regulated the glycolytic and pentose phosphate pathway genes. The PDC6 gene, previously thought to encode a minor isozyme of pyruvate decarboxylase, was highly induced under these conditions. Gene expression profiles indicate that the oxidative and non-oxidative branches of the pentose phosphate pathway were up-regulated and might be used to shunt more glucose-6-phosphate and fructose-6-phosphate, respectively, from the glycolytic pathway into the pentose phosphate pathway. Structural genes involved in the formation of acetic acid from acetaldehyde, and succinic acid from glutamate, were also up-regulated. Genes involved in de novo biosynthesis of purines, pyrimidines, histidine and lysine were down-regulated by sugar stress.</abstract><cop>Oxford, UK</cop><pub>Elsevier B.V</pub><pmid>12748050</pmid><doi>10.1016/S1567-1356(02)00203-9</doi><tpages>25</tpages></addata></record>
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subjects Acetaldehyde
Acetaldehyde - metabolism
Acetic acid
Acetic Acid - metabolism
Carbohydrate Metabolism
DNA array analysis
DNA microarrays
Fermentation
Fructose
Fructose-6-phosphate
Fungi
Gene expression
Gene Expression Profiling
Gene Expression Regulation, Fungal
Genomes
Glutamic Acid - metabolism
Glycolysis
Glycolysis - genetics
Glycolysis - physiology
Histidine
Lysine
Metabolic pathways
Metabolism
Oligonucleotide Array Sequence Analysis
Osmotic stress
Pentose phosphate pathway
Pentose Phosphate Pathway - genetics
Pentose Phosphate Pathway - physiology
Purines
Pyrimidines
Pyruvate decarboxylase
Pyruvic acid
RNA, Fungal - genetics
RNA, Fungal - metabolism
Saccharomyces cerevisiae
Saccharomyces cerevisiae - genetics
Saccharomyces cerevisiae - metabolism
Sorbitol
Succinic acid
Succinic Acid - metabolism
Sugar
Transcription
Transcription, Genetic - physiology
Wine
Yeast
title Genome-wide expression analyses: Metabolic adaptation of Saccharomyces cerevisiae to high sugar stress
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