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De novo production of the flavonoid naringenin in engineered Saccharomyces cerevisiae

Microbial cell factories, 2012-12, Vol.11 (1), p.155-155, Article 155

2012

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Vitamin requirements and biosynthesis in Saccharomyces cerevisiae

Yeast (Chichester, England), 2020-04, Vol.37 (4), p.283-304

2020

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CRISPR/Cas9: a molecular Swiss army knife for simultaneous introduction of multiple genetic modifications in Saccharomyces cerevisiae

FEMS yeast research, 2015-03, Vol.15 (2)

2015

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Engineering cytosolic acetyl-coenzyme A supply in Saccharomyces cerevisiae: Pathway stoichiometry, free-energy conservation and redox-cofactor balancing

Metabolic engineering, 2016-07, Vol.36, p.99-115

2016

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Industrial Relevance of Chromosomal Copy Number Variation in Saccharomyces Yeasts

Applied and environmental microbiology, 2017-06, Vol.83 (11), p.E03206

2017

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Pichia pastoris Exhibits High Viability and a Low Maintenance Energy Requirement at Near-Zero Specific Growth Rates

Applied and environmental microbiology, 2016-08, Vol.82 (15), p.4570-4583

2016

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Auxotrophic yeast strains in fundamental and applied research

Applied and environmental microbiology, 2002-05, Vol.68 (5), p.2095-2100

PRONK, Jack T

2002

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Genome duplication and mutations in ACE2 cause multicellular, fast-sedimenting phenotypes in evolved Saccharomyces cerevisiae

Proceedings of the National Academy of Sciences - PNAS, 2013-11, Vol.110 (45), p.E4223-E4231

2013

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Novel Evolutionary Engineering Approach for Accelerated Utilization of Glucose, Xylose, and Arabinose Mixtures by Engineered Saccharomyces cerevisiae Strains

Applied and Environmental Microbiology, 2009-02, Vol.75 (4), p.907-914

2009

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De novo sequencing, assembly and analysis of the genome of the laboratory strain Saccharomyces cerevisiae CEN.PK113-7D, a model for modern industrial biotechnology

Microbial cell factories, 2012-03, Vol.11 (1), p.36-36, Article 36

2012

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In vivo recombination of Saccharomyces eubayanus maltose-transporter genes yields a chimeric transporter that enables maltotriose fermentation

PLoS genetics, 2019-04, Vol.15 (4), p.e1007853

2019

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A versatile, efficient strategy for assembly of multi-fragment expression vectors in Saccharomyces cerevisiae using 60 bp synthetic recombination sequences

Microbial cell factories, 2013-05, Vol.12 (1), p.47-47, Article 47

2013

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Substrate Specificity of Thiamine Pyrophosphate-Dependent 2-Oxo-Acid Decarboxylases in Saccharomyces cerevisiae

Applied and Environmental Microbiology, 2012-11, Vol.78 (21), p.7538-7548

2012

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Malic Acid Production by Saccharomyces cerevisiae: Engineering of Pyruvate Carboxylation, Oxaloacetate Reduction, and Malate Export

Applied and Environmental Microbiology, 2008-05, Vol.74 (9), p.2766-2777

2008

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Laboratory Evolution of a Biotin-Requiring Saccharomyces cerevisiae Strain for Full Biotin Prototrophy and Identification of Causal Mutations

Applied and environmental microbiology, 2017-08, Vol.83 (16)

2017

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Replacement of the Saccharomyces cerevisiae acetyl-CoA synthetases by alternative pathways for cytosolic acetyl-CoA synthesis

Metabolic engineering, 2014-01, Vol.21, p.46-59

2014

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Transcriptome-Based Characterization of Interactions between Saccharomyces cerevisiae and Lactobacillus delbrueckii subsp. bulgaricus in Lactose-Grown Chemostat Cocultures

Applied and Environmental Microbiology, 2013-10, Vol.79 (19), p.5949-5961

2013

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Improving ethanol yield in acetate-reducing Saccharomyces cerevisiae by cofactor engineering of 6-phosphogluconate dehydrogenase and deletion of ALD6

Microbial cell factories, 2016-04, Vol.15 (1), p.67, Article 67

2016

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Elimination of Glycerol Production in Anaerobic Cultures of a Saccharomyces cerevisiae Strain Engineered To Use Acetic Acid as an Electron Acceptor

Applied and Environmental Microbiology, 2010-01, Vol.76 (1), p.190-195

2010

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An internal deletion in MTH1 enables growth on glucose of pyruvate-decarboxylase negative, non-fermentative Saccharomyces cerevisiae

Microbial cell factories, 2012-09, Vol.11 (1), p.131-131, Article 131

2012

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Engineering acetyl coenzyme A supply: functional expression of a bacterial pyruvate dehydrogenase complex in the cytosol of Saccharomyces cerevisiae

mBio, 2014-10, Vol.5 (5), p.e01696-e01614

2014

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Alcoholic fermentation of carbon sources in biomass hydrolysates by Saccharomyces cerevisiae: current status

Antonie van Leeuwenhoek, 2006-11, Vol.90 (4), p.391-418

2006

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Engineering of Saccharomyces cerevisiae for Efficient Anaerobic Alcoholic Fermentation of L-Arabinose

Applied and Environmental Microbiology, 2007-08, Vol.73 (15), p.4881-4891

2007

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The Genome-wide Transcriptional Responses of Saccharomyces cerevisiae Grown on Glucose in Aerobic Chemostat Cultures Limited for Carbon, Nitrogen, Phosphorus, or Sulfur

The Journal of biological chemistry, 2003-01, Vol.278 (5), p.3265-3274

2003

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fluxes through glycolytic enzymes in Saccharomyces cerevisiae are predominantly regulated at posttranscriptional levels

Proceedings of the National Academy of Sciences - PNAS, 2007-10, Vol.104 (40), p.15753-15758

2007

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De novo production of the flavonoid naringenin in engineered Saccharomyces cerevisiae

Vitamin requirements and biosynthesis in Saccharomyces cerevisiae

CRISPR/Cas9: a molecular Swiss army knife for simultaneous introduction of multiple genetic modifications in Saccharomyces cerevisiae

Engineering cytosolic acetyl-coenzyme A supply in Saccharomyces cerevisiae: Pathway stoichiometry, free-energy conservation and redox-cofactor balancing

Industrial Relevance of Chromosomal Copy Number Variation in Saccharomyces Yeasts

Pichia pastoris Exhibits High Viability and a Low Maintenance Energy Requirement at Near-Zero Specific Growth Rates

Auxotrophic yeast strains in fundamental and applied research

Genome duplication and mutations in ACE2 cause multicellular, fast-sedimenting phenotypes in evolved Saccharomyces cerevisiae

Novel Evolutionary Engineering Approach for Accelerated Utilization of Glucose, Xylose, and Arabinose Mixtures by Engineered Saccharomyces cerevisiae Strains

De novo sequencing, assembly and analysis of the genome of the laboratory strain Saccharomyces cerevisiae CEN.PK113-7D, a model for modern industrial biotechnology

In vivo recombination of Saccharomyces eubayanus maltose-transporter genes yields a chimeric transporter that enables maltotriose fermentation

A versatile, efficient strategy for assembly of multi-fragment expression vectors in Saccharomyces cerevisiae using 60 bp synthetic recombination sequences

Substrate Specificity of Thiamine Pyrophosphate-Dependent 2-Oxo-Acid Decarboxylases in Saccharomyces cerevisiae

Malic Acid Production by Saccharomyces cerevisiae: Engineering of Pyruvate Carboxylation, Oxaloacetate Reduction, and Malate Export

Laboratory Evolution of a Biotin-Requiring Saccharomyces cerevisiae Strain for Full Biotin Prototrophy and Identification of Causal Mutations

Replacement of the Saccharomyces cerevisiae acetyl-CoA synthetases by alternative pathways for cytosolic acetyl-CoA synthesis

Transcriptome-Based Characterization of Interactions between Saccharomyces cerevisiae and Lactobacillus delbrueckii subsp. bulgaricus in Lactose-Grown Chemostat Cocultures

Improving ethanol yield in acetate-reducing Saccharomyces cerevisiae by cofactor engineering of 6-phosphogluconate dehydrogenase and deletion of ALD6

Elimination of Glycerol Production in Anaerobic Cultures of a Saccharomyces cerevisiae Strain Engineered To Use Acetic Acid as an Electron Acceptor

An internal deletion in MTH1 enables growth on glucose of pyruvate-decarboxylase negative, non-fermentative Saccharomyces cerevisiae

Engineering acetyl coenzyme A supply: functional expression of a bacterial pyruvate dehydrogenase complex in the cytosol of Saccharomyces cerevisiae

Alcoholic fermentation of carbon sources in biomass hydrolysates by Saccharomyces cerevisiae: current status

Engineering of Saccharomyces cerevisiae for Efficient Anaerobic Alcoholic Fermentation of L-Arabinose

The Genome-wide Transcriptional Responses of Saccharomyces cerevisiae Grown on Glucose in Aerobic Chemostat Cultures Limited for Carbon, Nitrogen, Phosphorus, or Sulfur

fluxes through glycolytic enzymes in Saccharomyces cerevisiae are predominantly regulated at posttranscriptional levels

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