The capability to identify in a short time Brettanomyces bruxellensis, the yeast causing wine spoilage, is an important result both to increase quality of the products and to reduce economic losses in wineries. The development of a quick and specific method to detect B. bruxellensis in wine samples is a good tool for routine controls in wineries. Specific primers (DekITS and BruxITR) and a specific digoxygenin labelled probe were designed to be used in a PCR protocol and in a Dot blot method to detect B.bruxellensis in wine samples and/or to confirm isolates from wine samples. A molecular method, not requiring colony growth, is helpful for winemakers alike to quickly obtain information about the presence of Brettanomyces in their products. The results of this work indicate that the dot blot method is sensitive and fits this goal showing a great potential for its simple applicability. Both methods PCR and dot blot were useful for both a direct detection and a species specific confirmation of the isolates. © 2013 Elsevier Ltd.

Dot blot and PCR for Brettanomyces bruxellensis detection in red wine.

IACUMIN, Lucilla;COMUZZO, Piergiorgio;COMI, Giuseppe;MANZANO, Marisa
2013-01-01

Abstract

The capability to identify in a short time Brettanomyces bruxellensis, the yeast causing wine spoilage, is an important result both to increase quality of the products and to reduce economic losses in wineries. The development of a quick and specific method to detect B. bruxellensis in wine samples is a good tool for routine controls in wineries. Specific primers (DekITS and BruxITR) and a specific digoxygenin labelled probe were designed to be used in a PCR protocol and in a Dot blot method to detect B.bruxellensis in wine samples and/or to confirm isolates from wine samples. A molecular method, not requiring colony growth, is helpful for winemakers alike to quickly obtain information about the presence of Brettanomyces in their products. The results of this work indicate that the dot blot method is sensitive and fits this goal showing a great potential for its simple applicability. Both methods PCR and dot blot were useful for both a direct detection and a species specific confirmation of the isolates. © 2013 Elsevier Ltd.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11390/881094
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