Literature DB >> 26475113

Metabolic Impact of Redox Cofactor Perturbations on the Formation of Aroma Compounds in Saccharomyces cerevisiae.

Audrey Bloem1, Isabelle Sanchez2, Sylvie Dequin2, Carole Camarasa2.   

Abstract

Redox homeostasis is a fundamental requirement for the maintenance of metabolism, energy generation, and growth in Saccharomyces cerevisiae. The redox cofactors NADH and NADPH are among the most highly connected metabolites in metabolic networks. Changes in their concentrations may induce widespread changes in metabolism. Redox imbalances were achieved with a dedicated biological tool overexpressing native NADH-dependent or engineered NADPH-dependent 2,3-butanediol dehydrogenase, in the presence of acetoin. We report that targeted perturbation of the balance of cofactors (NAD(+)/NADH or, to a lesser extent, NADP(+)/NADPH) significantly affected the production of volatile compounds. In most cases, variations in the redox state of yeasts modified the formation of all compounds from the same biochemical pathway (isobutanol, isoamyl alcohol, and their derivatives) or chemical class (ethyl esters), irrespective of the cofactors. These coordinated responses were found to be closely linked to the impact of redox status on the availability of intermediates of central carbon metabolism. This was the case for α-keto acids and acetyl coenzyme A (acetyl-CoA), which are precursors for the synthesis of many volatile compounds. We also demonstrated that changes in the availability of NADH selectively affected the synthesis of some volatile molecules (e.g., methionol, phenylethanol, and propanoic acid), reflecting the specific cofactor requirements of the dehydrogenases involved in their formation. Our findings indicate that both the availability of precursors from central carbon metabolism and the accessibility of reduced cofactors contribute to cell redox status modulation of volatile compound formation.
Copyright © 2015, American Society for Microbiology. All Rights Reserved.

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Year:  2015        PMID: 26475113      PMCID: PMC4702612          DOI: 10.1128/AEM.02429-15

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  39 in total

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Authors:  Sofie M G Saerens; Kevin J Verstrepen; Stijn D M Van Laere; Arnout R D Voet; Patrick Van Dijck; Freddy R Delvaux; Johan M Thevelein
Journal:  J Biol Chem       Date:  2005-12-15       Impact factor: 5.157

2.  The effect of increased branched-chain amino acid transaminase activity in yeast on the production of higher alcohols and on the flavour profiles of wine and distillates.

Authors:  Mariska Lilly; Florian F Bauer; Gustav Styger; Marius G Lambrechts; Isak S Pretorius
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3.  Purification and properties of the 3-deoxy-D-arabino-heptulosonate-7-phosphate synthase (phenylalanine-inhibitable) of Saccharomyces cerevisiae.

Authors:  G Paravicini; T Schmidheini; G Braus
Journal:  Eur J Biochem       Date:  1989-12-08

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Authors:  G H Braus
Journal:  Microbiol Rev       Date:  1991-09

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Review 10.  Production and biological function of volatile esters in Saccharomyces cerevisiae.

Authors:  Sofie M G Saerens; Freddy R Delvaux; Kevin J Verstrepen; Johan M Thevelein
Journal:  Microb Biotechnol       Date:  2009-04-06       Impact factor: 5.813

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5.  Quantitative 13 C-isotope labelling-based analysis to elucidate the influence of environmental parameters on the production of fermentative aromas during wine fermentation.

Authors:  Stéphanie Rollero; Jean-Roch Mouret; Audrey Bloem; Isabelle Sanchez; Anne Ortiz-Julien; Jean-Marie Sablayrolles; Sylvie Dequin; Carole Camarasa
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6.  Linkage between Carbon Metabolism, Redox Status and Cellular Physiology in the Yeast Saccharomyces cerevisiae Devoid of SOD1 or SOD2 Gene.

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8.  PTR-MS Characterization of VOCs Associated with Commercial Aromatic Bakery Yeasts of Wine and Beer Origin.

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9.  Rerouting of NADPH synthetic pathways for increased protopanaxadiol production in Saccharomyces cerevisiae.

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10.  Tolerance and metabolic response of Pseudomonas taiwanensis VLB120 towards biomass hydrolysate-derived inhibitors.

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