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Fungal diversity in grape must and wine fermentation assessed by massive sequencing, quantitative PCR and DGGE

The diversity of fungi in grape must and during wine fermentation was investigated in this study by culture-dependent and culture-independent techniques. Carignan and Grenache grapes were harvested from three vineyards in the Priorat region (Spain) in 2012, and nine samples were selected from the gr...

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Autores principales: Wang, Chunxiao, García-Fernández, David, Mas, Albert, Esteve-Zarzoso, Braulio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615962/
https://www.ncbi.nlm.nih.gov/pubmed/26557110
http://dx.doi.org/10.3389/fmicb.2015.01156
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author Wang, Chunxiao
García-Fernández, David
Mas, Albert
Esteve-Zarzoso, Braulio
author_facet Wang, Chunxiao
García-Fernández, David
Mas, Albert
Esteve-Zarzoso, Braulio
author_sort Wang, Chunxiao
collection PubMed
description The diversity of fungi in grape must and during wine fermentation was investigated in this study by culture-dependent and culture-independent techniques. Carignan and Grenache grapes were harvested from three vineyards in the Priorat region (Spain) in 2012, and nine samples were selected from the grape must after crushing and during wine fermentation. From culture-dependent techniques, 362 isolates were randomly selected and identified by 5.8S-ITS-RFLP and 26S-D1/D2 sequencing. Meanwhile, genomic DNA was extracted directly from the nine samples and analyzed by qPCR, DGGE and massive sequencing. The results indicated that grape must after crushing harbored a high species richness of fungi with Aspergillus tubingensis, Aureobasidium pullulans, or Starmerella bacillaris as the dominant species. As fermentation proceeded, the species richness decreased, and yeasts such as Hanseniaspora uvarum, Starmerella bacillaris and Saccharomyces cerevisiae successively occupied the must samples. The “terroir” characteristics of the fungus population are more related to the location of the vineyard than to grape variety. Sulfur dioxide treatment caused a low effect on yeast diversity by similarity analysis. Because of the existence of large population of fungi on grape berries, massive sequencing was more appropriate to understand the fungal community in grape must after crushing than the other techniques used in this study. Suitable target sequences and databases were necessary for accurate evaluation of the community and the identification of species by the 454 pyrosequencing of amplicons.
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spelling pubmed-46159622015-11-09 Fungal diversity in grape must and wine fermentation assessed by massive sequencing, quantitative PCR and DGGE Wang, Chunxiao García-Fernández, David Mas, Albert Esteve-Zarzoso, Braulio Front Microbiol Microbiology The diversity of fungi in grape must and during wine fermentation was investigated in this study by culture-dependent and culture-independent techniques. Carignan and Grenache grapes were harvested from three vineyards in the Priorat region (Spain) in 2012, and nine samples were selected from the grape must after crushing and during wine fermentation. From culture-dependent techniques, 362 isolates were randomly selected and identified by 5.8S-ITS-RFLP and 26S-D1/D2 sequencing. Meanwhile, genomic DNA was extracted directly from the nine samples and analyzed by qPCR, DGGE and massive sequencing. The results indicated that grape must after crushing harbored a high species richness of fungi with Aspergillus tubingensis, Aureobasidium pullulans, or Starmerella bacillaris as the dominant species. As fermentation proceeded, the species richness decreased, and yeasts such as Hanseniaspora uvarum, Starmerella bacillaris and Saccharomyces cerevisiae successively occupied the must samples. The “terroir” characteristics of the fungus population are more related to the location of the vineyard than to grape variety. Sulfur dioxide treatment caused a low effect on yeast diversity by similarity analysis. Because of the existence of large population of fungi on grape berries, massive sequencing was more appropriate to understand the fungal community in grape must after crushing than the other techniques used in this study. Suitable target sequences and databases were necessary for accurate evaluation of the community and the identification of species by the 454 pyrosequencing of amplicons. Frontiers Media S.A. 2015-10-23 /pmc/articles/PMC4615962/ /pubmed/26557110 http://dx.doi.org/10.3389/fmicb.2015.01156 Text en Copyright © 2015 Wang, García-Fernández, Mas and Esteve-Zarzoso. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Wang, Chunxiao
García-Fernández, David
Mas, Albert
Esteve-Zarzoso, Braulio
Fungal diversity in grape must and wine fermentation assessed by massive sequencing, quantitative PCR and DGGE
title Fungal diversity in grape must and wine fermentation assessed by massive sequencing, quantitative PCR and DGGE
title_full Fungal diversity in grape must and wine fermentation assessed by massive sequencing, quantitative PCR and DGGE
title_fullStr Fungal diversity in grape must and wine fermentation assessed by massive sequencing, quantitative PCR and DGGE
title_full_unstemmed Fungal diversity in grape must and wine fermentation assessed by massive sequencing, quantitative PCR and DGGE
title_short Fungal diversity in grape must and wine fermentation assessed by massive sequencing, quantitative PCR and DGGE
title_sort fungal diversity in grape must and wine fermentation assessed by massive sequencing, quantitative pcr and dgge
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615962/
https://www.ncbi.nlm.nih.gov/pubmed/26557110
http://dx.doi.org/10.3389/fmicb.2015.01156
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