
doi: 10.1002/bit.20020
pmid: 15083505
AbstractCentral carbon metabolism of the yeast Saccharomyces cerevisiae was analyzed using metabolic pathway analysis tools. Elementary flux modes for three substrates (glucose, galactose, and ethanol) were determined using the catabolic reactions occurring in yeast. Resultant elementary modes were used for gene deletion phenotype analysis and for the analysis of robustness of the central metabolism and network functionality. Control‐effective fluxes, determined by calculating the efficiency of each mode, were used for the prediction of transcript ratios of metabolic genes in different growth media (glucose–ethanol and galactose–ethanol). A high correlation was obtained between the theoretical and experimental expression levels of 38 genes when ethanol and glucose media were considered. Such analysis was shown to be a bridge between transcriptomics and fluxomics. Control‐effective flux distribution was found to be promising in in silico predictions by incorporating functionality and regulation into the metabolic network structure. © 2004 Wiley Periodicals, Inc.
Ethanol, Transcription, Genetic, Genes, Fungal, Galactose, Saccharomyces cerevisiae, Models, Biological, Carbon, Culture Media, Glucose, Gene Expression Regulation, Fungal, Biomass, Gene Deletion
Ethanol, Transcription, Genetic, Genes, Fungal, Galactose, Saccharomyces cerevisiae, Models, Biological, Carbon, Culture Media, Glucose, Gene Expression Regulation, Fungal, Biomass, Gene Deletion
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 67 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
