Use of chemostat cultures mimicking different phases of wine fermentations as a tool for quantitative physiological analysis

  1. Vázquez-Lima, F. 25
  2. Silva, P. 23
  3. Barreiro, A. 12
  4. Martínez-Moreno, R. 678
  5. Morales, P. 6
  6. Quirós, M. 46
  7. González, R. 6
  8. Albiol, J. 2
  9. Ferrer, P. 24
  1. 1 Bioingenium s.l, Barcelona, Catalonia, Spain
  2. 2 Universitat Autònoma de Barcelona
    info

    Universitat Autònoma de Barcelona

    Barcelona, España

    ROR https://ror.org/052g8jq94

  3. 3 Pontificia Universidad Católica de Valparaíso
    info

    Pontificia Universidad Católica de Valparaíso

    Valparaíso, Chile

    ROR https://ror.org/02cafbr77

  4. 4 Evolva Biotech A/S, Copenhagen, Denmark
  5. 5 Greenaltech s.l, Barcelona, Catalonia, Spain
  6. 6 Instituto de Ciencias de la Vid y del Vino
    info

    Instituto de Ciencias de la Vid y del Vino

    Logroño, España

    ROR https://ror.org/01rm2sw78

  7. 7 Quercus Europe s.l., L'Hospitalet de Llobregat, Catalonia, Spain
  8. 8 Universidad Internacional de La Rioja
    info

    Universidad Internacional de La Rioja

    Logroño, España

    ROR https://ror.org/029gnnp81

Journal:
Microbial Cell Factories

ISSN: 1475-2859

Year of publication: 2014

Volume: 13

Issue: 1

Pages: 1-13

Type: Article

beta Ver similares en nube de resultados
DOI: 10.1186/1475-2859-13-85 SCOPUS: 2-s2.0-84902061617 WoS: WOS:000338261500001 GOOGLE SCHOLAR lock_openOpen access editor

More publications in: Microbial Cell Factories

Institutional repository: lock_openOpen access Editor

Abstract

Background: Saccharomyces cerevisiae is the most relevant yeast species conducting the alcoholic fermentation that takes place during winemaking. Although the physiology of this model organism has been extensively studied, systematic quantitative physiology studies of this yeast under winemaking conditions are still scarce, thus limiting the understanding of fermentative metabolism of wine yeast strains and the systematic description, modelling and prediction of fermentation processes. In this study, we implemented and validated the use of chemostat cultures as a tool to simulate different stages of a standard wine fermentation, thereby allowing to implement metabolic flux analyses describing the sequence of metabolic states of S. cerevisae along the wine fermentation.Results: Chemostat cultures mimicking the different stages of standard wine fermentations of S. cerevisiae EC1118 were performed using a synthetic must and strict anaerobic conditions. The simulated stages corresponded to the onset of the exponential growth phase, late exponential growth phase and cells just entering stationary phase, at dilution rates of 0.27, 0.04, 0.007 h-1, respectively. Notably, measured substrate uptake and product formation rates at each steady state condition were generally within the range of corresponding conversion rates estimated during the different batch fermentation stages.Moreover, chemostat data were further used for metabolic flux analysis, where biomass composition data for each condition was considered in the stoichiometric model. Metabolic flux distributions were coherent with previous analyses based on batch cultivations data and the pseudo-steady state assumption.Conclusions: Steady state conditions obtained in chemostat cultures reflect the environmental conditions and physiological states of S. cerevisiae corresponding to the different growth stages of a typical batch wine fermentation, thereby showing the potential of this experimental approach to systematically study the effect of environmental relevant factors such as temperature, sugar concentration, C/N ratio or (micro) oxygenation on the fermentative metabolism of wine yeast strains. © 2014 Vázquez-Lima et al.; licensee BioMed Central Ltd.