Redirection of the respiro-fermentative flux distribution in Saccharomyces cerevisiae by overexpression of the transcription factor Hap4p - Wikidata - wikimedia - TriplyDB

Redirection of the respiro-fermentative flux distribution in Saccharomyces cerevisiae by overexpression of the transcription factor Hap4p

Redirection of the respiro-fermentative flux distribution in Saccharomyces cerevisiae by overexpression of the transcription factor Hap4p

http://www.wikidata.org/entity/Q39536241

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Hap4p overexpression in glucose-grown Saccharomyces cerevisiae induces cells to enter a novel metabolic state Validation and refinement of gene-regulatory pathways on a network of physical interactions Physiological adaptations of Saccharomyces cerevisiae evolved for improved butanol tolerance Increased glycolytic flux as an outcome of whole-genome duplication in yeast Fluxomics - connecting ‘omics analysis and phenotypes Osmotic stress signaling and osmoadaptation in yeasts.Integrative investigation of metabolic and transcriptomic data Integration of metabolic modeling and phenotypic data in evaluation and improvement of ethanol production using respiration-deficient mutants of Saccharomyces cerevisiae.Gene transcription analysis of Saccharomyces cerevisiae exposed to neocarzinostatin protein-chromophore complex reveals evidence of DNA damage, a potential mechanism of resistance, and consequences of prolonged exposure Calorie restriction extends yeast life span by lowering the level of NADH.Minimization of glycerol production during the high-performance fed-batch ethanolic fermentation process in Saccharomyces cerevisiae, using a metabolic model as a prediction tool Functional study of the Hap4-like genes suggests that the key regulators of carbon metabolism HAP4 and oxidative stress response YAP1 in yeast diverged from a common ancestor.Mechanistic study on the nuclear modifier gene MSS1 mutation suppressing neomycin sensitivity of the mitochondrial 15S rRNA C1477G mutation in Saccharomyces cerevisiae Modular pathway rewiring of Saccharomyces cerevisiae enables high-level production of L-ornithine.Reduced Histone Expression or a Defect in Chromatin Assembly Induces Respiration.The S. Cerevisiae HAP complex, a key regulator of mitochondrial function, coordinates nuclear and mitochondrial gene expression.Overexpression of a Water-Forming NADH Oxidase Improves the Metabolism and Stress Tolerance of Saccharomyces cerevisiae in Aerobic Fermentation.GSF2 deletion increases lactic acid production by alleviating glucose repression in Saccharomyces cerevisiae.The transcription factors ADR1 or CAT8 are required for RTG pathway activation and evasion from yeast acetic acid-induced programmed cell death in raffinose.A flux-sensing mechanism could regulate the switch between respiration and fermentation.Improved properties of baker's yeast mutants resistant to 2-deoxy-D-glucose.Directed evolution of pyruvate decarboxylase-negative Saccharomyces cerevisiae, yielding a C2-independent, glucose-tolerant, and pyruvate-hyperproducing yeast.An internal deletion in MTH1 enables growth on glucose of pyruvate-decarboxylase negative, non-fermentative Saccharomyces cerevisiae.Shifting the fermentative/oxidative balance in Saccharomyces cerevisiae by transcriptional deregulation of Snf1 via overexpression of the upstream activating kinase Sak1p Reactive oxygen species-mediated control of mitochondrial biogenesis.Switching the mode of sucrose utilization by Saccharomyces cerevisiae.Longevity: don't hold your breath.The yeast mitochondrial proteome, a study of fermentative and respiratory growth.Saccharomyces cerevisiae glutaredoxin 5-deficient cells subjected to continuous oxidizing conditions are affected in the expression of specific sets of genes.Dynamic effects related to steady-state multiplicity in continuous Saccharomyces cerevisiae cultivations.Fermentative metabolism impedes p53-dependent apoptosis in a Crabtree-positive but not in Crabtree-negative yeast.Increased heme synthesis in yeast induces a metabolic switch from fermentation to respiration even under conditions of glucose repression.Two-dimensional transcriptome analysis in chemostat cultures. Combinatorial effects of oxygen availability and macronutrient limitation in Saccharomyces cerevisiae.The impact of MIG1 and/or MIG2 disruption on aerobic metabolism of succinate dehydrogenase negative Saccharomyces cerevisiae.Stoichiometry and compartmentation of NADH metabolism inSaccharomyces cerevisiae Dissection of the promoter of theHAP4 gene inS. cerevisiae unveils a complex regulatory framework of transcriptional regulation

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P2860

Redirection of the respiro-fermentative flux distribution in Saccharomyces cerevisiae by overexpression of the transcription factor Hap4p

http://www.wikidata.org/entity/Q39536241

description

2000 nî lūn-bûn

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2000年の論文

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2000年論文

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2000年论文

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Redirection of the respiro-fer ...... the transcription factor Hap4p

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Redirection of the respiro-fer ...... he transcription factor Hap4p.

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Redirection of the respiro-fer ...... the transcription factor Hap4p

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Redirection of the respiro-fer ...... he transcription factor Hap4p.

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Redirection of the respiro-fer ...... the transcription factor Hap4p

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Redirection of the respiro-fer ...... he transcription factor Hap4p.

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AEM.66.5.1970-1973.2000

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Applied and Environmental Microbiology

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Redirection of the respiro-fer ...... the transcription factor Hap4p

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J Blom

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L A Grivell

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M J De Mattos

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P2860

Transformation of intact yeast cells treated with alkali cations

Exploring the metabolic and genetic control of gene expression on a genomic scale

Subunit II of yeast QH2:cytochrome-c oxidoreductase. Nucleotide sequence of the gene and features of the protein.

Glucose derepression of gluconeogenic enzymes in Saccharomyces cerevisiae correlates with phosphorylation of the gene activator Cat8p.

Identification and characterization of HAP4: a third component of the CCAAT-bound HAP2/HAP3 heteromer.

New yeast-Escherichia coli shuttle vectors constructed with in vitro mutagenized yeast genes lacking six-base pair restriction sites

Systematic determination of genetic network architecture

Exploring the new world of the genome with DNA microarrays

Alleviation of glucose repression of maltose metabolism by MIG1 disruption in Saccharomyces cerevisiae.

Live control of the living cell.

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Saccharomyces cerevisiae

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101441

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