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Polymorphism detection among wild Saccharomyces cerevisiae strains of different wine origin

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Abstract

In this study, wild Saccharomyces cerevisiae strains, isolated from spontaneously fermenting grapes of different varieties and origins, were submitted to genetic analysis using different molecular techniques, such as amplification of genes coding for cell wall proteins and containing minisatellite-like sequences, karyotyping, mtDNA-RFLP, and analysis of the δ region. The lowest discriminative power was obtained by minisatellites analysis, in particular the amplification of AGA1 genes. Karyotyping and mtDNA-RFLP analysis yielded the same differentiation among the strains, whereas the PCR amplification of δ sequences resulted the best method as it was fast and it showed a very high discriminative power. In any case, it has to be underlined that some strains, showing the same delta profiles, exhibited a different mtDNA restriction profile and electrophoretic karyotype, suggesting that more than one molecular marker is required for reliable strain discrimination. Although the techniques used revealed a different resolution power, they all revealed a genetic relationship among strains isolated from spontaneous fermentation of grapes of different origins. In fact, none of the typing methods was able to discriminate some strains isolated from different areas.

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Authors and Affiliations

  1. Dipartimento Biologia, Difesa e Biotecnologie Agro-forestali, Università degli Studi della Basilicata, Viale dell’Ateneo Lucano 10, 85100, Potenza, Italy

    Gabriella Siesto, Angela Capece & Patrizia Romano

  2. Department of Genetics and Applied Microbiology, University of Debrecen, Debrecen, Hungary

    Matthias Sipiczki & Hajnalka Csoma

Authors
  1. Gabriella Siesto
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  2. Angela Capece
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  3. Matthias Sipiczki
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  4. Hajnalka Csoma
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  5. Patrizia Romano
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Correspondence to Angela Capece.

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Siesto, G., Capece, A., Sipiczki, M. et al. Polymorphism detection among wild Saccharomyces cerevisiae strains of different wine origin. Ann Microbiol 63, 661–668 (2013). https://doi.org/10.1007/s13213-012-0516-6

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  • DOI: https://doi.org/10.1007/s13213-012-0516-6

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