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Wiley InterScience

FEMS Yeast Research

FEMS Yeast Research

Volume 6 Issue 1, Pages 91 - 101

Published Online: 6 Oct 2005

© 2010 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved



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Metabolic profiling as a tool for revealing Saccharomyces interactions during wine fermentation
Kate S. Howell 1,2 , Daniel Cozzolino 2,3 , Eveline J. Bartowsky 2 , Graham H. Fleet 1 & Paul A. Henschke 2
  1 Food Science and Technology, School of Chemical Engineering and Industrial Chemistry, University of New South Wales, Sydney, NSW, Australia;   2 The Australian Wine Research Institute, Glen Osmond, Adelaide, SA, Australia; and   3 The Cooperative Research Centre for Viticulture, Glen Osmond, Adelaide, SA, Australia
 Correspondence: Paul A. Henschke, The Australian Wine Research Institute, PO Box 197, Glen Osmond, Adelaide SA 5064, Australia. Tel.: +61 8 8303 6600; fax: +61 8 8303 6601; e-mail: paul.henschke@awri.com.au

 Editor: Lex Scheffers

Copyright © 2005 Federation of European Microbiological Societies
KEYWORDS
wine fermentation • principal-component analysis • ecology • aroma • metabolic profiling • Saccharomyces bayanusSaccharomyces cerevisiae

ABSTRACT

The multi-yeast strain composition of wine fermentations has been well established. However, the effect of multiple strains of Saccharomyces spp. on wine flavour is unknown. Here, we demonstrate that multiple strains of Saccharomyces grown together in grape juice can affect the profile of aroma compounds that accumulate during fermentation. A metabolic footprint of each yeast in monoculture, mixed cultures or blended wines was derived by gas chromatography – mass spectrometry measurement of volatiles accumulated during fermentation. The resultant ion spectrograms were transformed and compared by principal-component analysis. The principal-component analysis showed that the profiles of compounds present in wines made by mixed-culture fermentation were different from those where yeasts were grown in monoculture fermentation, and these differences could not be produced by blending wines. Blending of monoculture wines to mimic the population composition of mixed-culture wines showed that yeast metabolic interactions could account for these differences. Additionally, the yeast strain contribution of volatiles to a mixed fermentation cannot be predicted by the population of that yeast. This study provides a novel way to measure the population status of wine fermentations by metabolic footprinting.


Received 8 March 2005; revised 18 July 2005; accepted 28 July 2005.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1567-1364.2005.00010.x About DOI

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