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Yeast viability during fermentation and sur lie ageing of a defined medium and subsequent growth of Oenococcus oeni

Yeast viability during fermentation and sur lie ageing of a defined medium and subsequent growth of Oenococcus oeni
Yeast viability during fermentation and sur lie ageing of a defined medium and subsequent growth of Oenococcus oeni

Interactions between the yeast strain used for primary oenological fermentation and the bacterium used to conduct subsequent malolactic fermentation were studied under model winemaking conditions. A commercial Saccharomyces cerevisiae wine yeast (strains, EC 1118, AWRI 835 and CY-3079) was grown in a defined medium whose composition approximated grape juice. Fermentations by all strains reached dryness, and retained a cell viability of greater than 90% upon completion of fermentation. Highest total viable cell number and percentage of viable cells were recorded for EC 1118. A sur lie ageing of the fermented medium over a 12 week period revealed a bi-phasic decay of culture viability for all strains. Thus 99% of cells had died within 2 weeks post-fermentation. Viabilities were then stable for the subsequent 4-6 week period before a second decline phase ensued and ended in either a minimal (ca 100 CFU/mL, EC 1118) or no viable cells being detected at 12 weeks of ageing. The growth response of an Oenococcus oeni inoculum to yeast culture supernatants, previously aged for up to 12 weeks in the presence or absence of yeast lees, was evaluated in a bio-assay. In this way, yeast strains could be designated as being either inhibitory, neutral or stimulatory to the growth of O. oeni (strain Lc5p). Inhibition by supernatants of strain EC 1118 was evident, but found to be reduced by ageing the supernatant (with or without lees). Conversely, longer ageing on yeast lees increased the magnitude of the stimulatory response in O. oeni (strain Lc5p) to the supernatant from the wine yeast (strain CY-3079).

Lees ageing, Microbial interactions, Oenococcus oeni, Saccharomyces cerevisiae, Wine
1322-7130
62-69
Patynowski, Robert J.
fcfe4776-c8c3-422b-8157-94dba4ab5c64
Jiranek, Vladimir
8e5a8dfd-f5b2-43e3-928b-11dff324abc7
Markides, Andrew J.
51c03521-4a06-48a1-87eb-9329b450b284
Patynowski, Robert J.
fcfe4776-c8c3-422b-8157-94dba4ab5c64
Jiranek, Vladimir
8e5a8dfd-f5b2-43e3-928b-11dff324abc7
Markides, Andrew J.
51c03521-4a06-48a1-87eb-9329b450b284

Patynowski, Robert J., Jiranek, Vladimir and Markides, Andrew J. (2002) Yeast viability during fermentation and sur lie ageing of a defined medium and subsequent growth of Oenococcus oeni. Australian Journal of Grape and Wine Research, 8 (1), 62-69. (doi:10.1111/j.1755-0238.2002.tb00212.x).

Record type: Article

Abstract

Interactions between the yeast strain used for primary oenological fermentation and the bacterium used to conduct subsequent malolactic fermentation were studied under model winemaking conditions. A commercial Saccharomyces cerevisiae wine yeast (strains, EC 1118, AWRI 835 and CY-3079) was grown in a defined medium whose composition approximated grape juice. Fermentations by all strains reached dryness, and retained a cell viability of greater than 90% upon completion of fermentation. Highest total viable cell number and percentage of viable cells were recorded for EC 1118. A sur lie ageing of the fermented medium over a 12 week period revealed a bi-phasic decay of culture viability for all strains. Thus 99% of cells had died within 2 weeks post-fermentation. Viabilities were then stable for the subsequent 4-6 week period before a second decline phase ensued and ended in either a minimal (ca 100 CFU/mL, EC 1118) or no viable cells being detected at 12 weeks of ageing. The growth response of an Oenococcus oeni inoculum to yeast culture supernatants, previously aged for up to 12 weeks in the presence or absence of yeast lees, was evaluated in a bio-assay. In this way, yeast strains could be designated as being either inhibitory, neutral or stimulatory to the growth of O. oeni (strain Lc5p). Inhibition by supernatants of strain EC 1118 was evident, but found to be reduced by ageing the supernatant (with or without lees). Conversely, longer ageing on yeast lees increased the magnitude of the stimulatory response in O. oeni (strain Lc5p) to the supernatant from the wine yeast (strain CY-3079).

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More information

Published date: 2002
Keywords: Lees ageing, Microbial interactions, Oenococcus oeni, Saccharomyces cerevisiae, Wine

Identifiers

Local EPrints ID: 482554
URI: http://eprints.soton.ac.uk/id/eprint/482554
ISSN: 1322-7130
PURE UUID: 97578821-14e7-40fb-aa1f-038ff8cad097
ORCID for Vladimir Jiranek: ORCID iD orcid.org/0000-0002-9775-8963

Catalogue record

Date deposited: 10 Oct 2023 16:58
Last modified: 18 Mar 2024 04:12

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Contributors

Author: Robert J. Patynowski
Author: Vladimir Jiranek ORCID iD
Author: Andrew J. Markides

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