Regulation of central carbon metabolism in Saccharomyces cerevisiae by metabolic inhibitors(MICROBIAL PHYSIOLOGY AND BIOTECHNOLOGY)
スポンサーリンク
概要
- 論文の詳細を見る
Metabolic inhibitors were applied for chemical regulation of central carbon metabolism in Saccharomyces cerevisiae. S. cerevisiae was treated with 10 metabolic inhibitors with various modes of action, and their activities were evaluated using a growth inhibition assay. Among the 6 active inhibitors, the effects of pyrazole (alcohol dehydrogenase inhibitor) and TTA (2-thenoyltrifluoloacetone, succinate dehydrogenase inhibitor) were analyzed in detail. The flask-scale batch-fermentation test showed that ethanol yield was reduced to 0.10 ± 0.01 g g^<-1> and glycerol yield increased to 0.26 ± 0.01 g g^<-1> on treatment with pyrazole at 5.0 g L-^<1>, indicating that multiple isozymes of alcohol dehydrogenase were simultaneously inhibited. The multi-targeted metabolic profiling analysis revealed that, although the TTA and pyrazole treatments affected the profiles of all central carbon metabolites in distinct manners, the level of fructose-1,6-bisphosphate commonly increased in the TTA- and pyrazole-treated S. cerevisiae by an unknown mechanism. These results demonstrate that chemical regulation of the central carbon metabolism could be used as an alternative tool to control microbial cell factories for bioproduction, or as a chemical probe to investigate the metabolic systems of useful microorganisms.
- 2013-07-00
著者
-
Kondo Akihiko
Organization of Advanced Science and Technology, Kobe University
-
Ishii Jun
Organization Of Advanced Science And Technology Kobe University
-
Matsuda Fumio
Organization Of Advanced Science And Technology Kobe University
-
Kondo Akihiko
Organization of Advanced Science and Technology, Kobe University:RIKEN Biomass Engineering Program:Department of Chemical Science and Engineering, Graduate School of Engineering, Kobe University
-
Shirai Tomokazu
RIKEN Biomass Engineering Program
関連論文
- EP-O1 Enzyme-mediated site-specific protein modification(Section VII Enzyme and Protein Engineering)
- MN-P30 Expression and signaling analyses of human G protein-coupled receptor in yeast(Section X Micro/Nano Technology for Analysis and Cell Manipulation)
- MN-P18 Investigation of the interaction between GPCR and ligand by AFM equipped with bio-molecule modified cantilever(Section X Micro/Nano Technology for Analysis and Cell Manipulation)
- EP-P28 Functional analysis of mutant human somatostatin receptor using a yeast-based fluorescence reporter assay(Section VII Enzyme and Protein Engineering)
- BE-O13 Construction of a novel detection system for protein-protein interactions using yeast G-protein signaling(Section V Biomolecular Engineering and Bioseparation)
- BR-P27 Bioethaol fermentation from mixed sugar by the recombinant yeast with xyloseisomerase pathway(Section IV Biorefinery)
- Yeast-Based Fluorescence Reporter Assay of G Protein-coupled Receptor Signalling for Flow Cytometric Screening : FAR1-Disruption Recovers Loss of Episomal Plasmid Caused by Signalling in Yeast
- A Simple and Immediate Method for Simultaneously Evaluating Expression Level and Plasmid Maintenance in Yeast
- Control of signalling properties of human somatostatin receptor subtype-5 by additional signal sequences on its amino-terminus in yeast
- Importance of asparagine residues at positions 13 and 26 on the amino-terminal domain of human somatostatin receptor subtype-5 in signalling
- BM-P13 Split-ubiquitin system for analyzing oligomerization of G protein-coupled receptor(Section III Biomedical Engineering)
- Variation in Biomass Properties among Rice Diverse Cultivars
- Comparative Profiling Analysis of Central Metabolites in Euglena gracilis under Various Cultivation Conditions
- Widely targeted metabolic profiling analysis of yeast central metabolites(METHODS)
- Comparative Profiling Analysis of Central Metabolites in Euglena gracilis under Various Cultivation Conditions
- Widely targeted metabolic profiling analysis of yeast central metabolites
- Regulation of central carbon metabolism in Saccharomyces cerevisiae by metabolic inhibitors(MICROBIAL PHYSIOLOGY AND BIOTECHNOLOGY)
- Construction of an Artificial Pathway for Isobutanol Biosynthesis in the Cytosol of Saccharomyces cerevisiae
- Cocktail δ-integration of xylose assimilation genes for efficient ethanol production from xylose in Saccharomyces cerevisiae(MICROBIAL PHYSIOLOGY AND BIOTECHNOLOGY)
- Utilization of Lactic Acid Bacterial Genes in Synechocystis sp. PCC 6803 in the Production of Lactic Acid