1995
DOI: 10.1128/aem.61.10.3521-3529.1995
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Genetic diversity and geographical distribution of wild Saccharomyces cerevisiae strains from the wine-producing area of Charentes, France

Abstract: Electrophoretic karyotyping, mitochondrial DNA restriction fragment length polymorphism analysis, and PCR amplification of interspersed repeats were used to study the variability, phylogenetic affinities, and biogeographic distribution of wild Saccharomyces cerevisiae enological yeasts. The survey concentrated on 42 individual wine cellars in the Charentes area (Cognac region, France). A limited number (35) of predominant S. cerevisiae strains responsible for the fermentation process have been identified by th… Show more

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Cited by 152 publications
(127 citation statements)
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References 12 publications
(22 reference statements)
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“…The large majority of the 104 chromosomal patterns of S. cerevisiae strains identified were unique, demonstrating an enormous biodiversity of indigenous S. cerevisiae strains in this region of France. Considering the ratio between the number of Saccharomyces isolates and the number of patterns as an approximate biodiversity estimation, our overall results (about six strains per pattern) showed similar values to those found in Portugal by Schuller et al (2005) and in previously published studies on the genetic diversity of indigenous S. cerevisiae strains in other viticultural regions of France (Vézinhet et al, 1992;Versavaud et al, 1995). In our study, this general estimation includes different situations, in contrast to the Portuguese results, where no apparent correlation between the number of strains involved in a fermentation and sampling site, year or vineyard was found .…”
Section: Discussionsupporting
confidence: 88%
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“…The large majority of the 104 chromosomal patterns of S. cerevisiae strains identified were unique, demonstrating an enormous biodiversity of indigenous S. cerevisiae strains in this region of France. Considering the ratio between the number of Saccharomyces isolates and the number of patterns as an approximate biodiversity estimation, our overall results (about six strains per pattern) showed similar values to those found in Portugal by Schuller et al (2005) and in previously published studies on the genetic diversity of indigenous S. cerevisiae strains in other viticultural regions of France (Vézinhet et al, 1992;Versavaud et al, 1995). In our study, this general estimation includes different situations, in contrast to the Portuguese results, where no apparent correlation between the number of strains involved in a fermentation and sampling site, year or vineyard was found .…”
Section: Discussionsupporting
confidence: 88%
“…With respect to the impact of the utilization of commercial yeast as a fermentation starter in the wineries, our study appears to show that the biodiversity of autochthonous species of S. cerevisiae remains very close to that reported in other studies, including fermentations in wineries where no commercial wine yeast strains have been used (Frezier & Dubourdieu, 1992;Vézinhet et al, 1992;Versavaud et al, 1995;Sabate et al, 1998;Torija et al, 2001). Furthermore, the fact that we found very different levels of biodiversity in the three vineyards studied (A, B and C) around the wineries that had utilized commercial yeast in large quantities for a long time verifies that other factors were more important than commercial yeast utilization for the biodiversity of the vineyard.…”
Section: Discussionsupporting
confidence: 82%
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“…Genetic studies have shown significant differences among commercial and laboratory S. cerevisiae strains (Benitez et al, 1996;Mortimer, 2000;Dunn et al, 2005). Whereas most strains used in the laboratory have a defined set of chromosome lengths and are haploid or diploid, frequently investigated yeasts associated with alcoholic fermentation show chromosomal alterations and variations in ploidy (Versavaud et al, 1995;Miklos et al, 1997;Rachidi et al, 1999). Wine yeasts may exhibit genetic instability with gross chromosomal rearrangements, chromosome length polymorphisms and may be polyploid or aneuploid (Dunham et al, 2002;Naumova et al, 2005;Bradbury et al, 2006).…”
Section: Introductionmentioning
confidence: 99%
“…Many methods were developed and applied for such purposes. Methods like karyotyping based on chromosome length polymorphism, or mitochondrial DNA polymorphism are the most widely used (Querol et al 1992;Versavaud et al 1995;Nadal et al 1996;Comi et al 2000;Lopez et al 2001), but they can be cumbersome and time-consuming. Several polymerase chain reaction (PCR)-based techniques were proposed, like random amplified polymorphic DNA (RAPD) associated or not with restriction analysis (Quesada and Cenis 1995;Perez et al 2001) or with sequencing (McGrath et al 1998), amplification of introns of the mitochondrial gene COX1 or using intron splice site primers (de Barros Lopes et al 1996;Lopez et al 2003), amplification of genomic regions using primers associated with delta elements of retrotransposons (Ness et al 1993;Legras and Karst 2003), or fingerprinting of microsatellite markers (Gallego et al 1998;Hennequin et al 2001;Legras et al 2005).…”
Section: Introductionmentioning
confidence: 99%