ArticleApplied and environmental microbiology2005
Engineering of a novel Saccharomyces cerevisiae wine strain with a respiratory phenotype at high external glucose concentrations.
Article in Applied and environmental microbiology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed, 38 citations in OpenAlex.
- Yeast as a tool for membrane protein production and structure determination.FEMS yeast research · 2022Article
- Metabolic Engineering of Wine Strains ofGenes · 2020Review
- Yeast's balancing act between ethanol and glycerol production in low-alcohol wines.Microbial biotechnology · 2017Review
- Identification of target genes to control acetate yield during aerobic fermentation with Saccharomyces cerevisiae.Microbial cell factories · 2016Article
- Yeast as a cell factory: current state and perspectives.Microbial cell factories · 2015Review
- The impact of oxygen on the final alcohol content of wine fermented by a mixed starter culture.Applied microbiology and biotechnology · 2015Article
- Evaluation of gene modification strategies for the development of low-alcohol-wine yeasts.Applied and environmental microbiology · 2012Article
- Shifting the fermentative/oxidative balance in Saccharomyces cerevisiae by transcriptional deregulation of Snf1 via overexpression of the upstream activating kinase Sak1p.Applied and environmental microbiology · 2011Article
- Increasing cell biomass in Saccharomyces cerevisiae increases recombinant protein yield: the use of a respiratory strain as a microbial cell factory.Microbial cell factories · 2010Article
- Altering the ribosomal subunit ratio in yeast maximizes recombinant protein yield.Microbial cell factories · 2009Article
- Progress in metabolic engineering of Saccharomyces cerevisiae.Microbiology and molecular biology reviews : MMBR · 2008Review
- Article
- Switching the mode of sucrose utilization by Saccharomyces cerevisiae.Microbial cell factories · 2008Article
Corrections and comments
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Authors and funding
9 authors at 4 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The recently described respiratory strain Saccharomyces cerevisiae KOY.TM6*P is, to our knowledge, the only reported strain of S. cerevisiae which completely redirects the flux of glucose from ethanol fermentation to respiration, even at high external glucose concentrations (27). In the KOY.TM6*P strain, portions of the genes encoding the predominant hexose transporter proteins, Hxt1 and Hxt7, were fused within the regions encoding transmembrane (TM) domain 6. The resulting chimeric gene, TM6*, encoded a chimera composed of the amino-terminal half of Hxt1 and the carboxy-terminal half of Hxt7. It was subsequently integrated into the genome of an hxt null strain. In this study, we have demonstrated the transferability of this respiratory phenotype to the V5 hxt1-7Delta strain, a derivative of a strain used in enology. We also show by using this mutant that it is not necessary to transform a complete hxt null strain with the TM6* construct to obtain a non-ethanol-producing phenotype. The resulting V5.TM6*P strain, obtained by transformation of the V5 hxt1-7Delta strain with the TM6* chimeric gene, produced only minor amounts of ethanol when cultured on external glucose concentrations as high as 5%. Despite the fact that glucose flux was reduced to 30% in the V5.TM6*P strain compared with that of its parental strain, the V5.TM6*P strain produced biomass at a specific rate as high as 85% that of the V5 wild-type strain. Even more relevant for the potential use of such a strain for the production of heterologous proteins and also of low-alcohol beverages is the observation that the biomass yield increased 50% with the mutant compared to its parental strain.
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