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Molecular identification and genetic diversity within species of the genera Hanseniaspora and Kloeckera
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Three molecular methods, RAPD-PCR analysis, electrophoretic karyotyping and RFLP of the PCR-amplified ITS regions (ITS1, ITS2 and the intervening 5.8S rDNA), were studied for accurate identification of Hanseniaspora and Kloeckera species as well as for determining inter- and intraspecific relationships of 74 strains isolated from different sources and/or geographically distinct regions. Of these three methods, PCR-RFLP analysis of ITS regions with restriction enzymes DdeI and HinfI is proposed as a rapid identification method to discriminate unambiguously between all six Hanseniaspora species and the single non-ascospore-forming apiculate yeast species Kloeckera lindneri. Electrophoretic karyotyping produced chromosomal profiles by which the seven species could be divided into four groups sharing similar karyotypes. Although most of the 60 strains examined exhibited a common species-specific pattern, a different degree of chromosomal-length polymorphism and a variable number of chromosomal DNA fragments were observed within species. Cluster analysis of the combined RAPD-PCR fingerprints obtained with one 10-mer primer, two microsatellite primers and one minisatellite primer generated clusters which with a few exceptions are in agreement with the groups as earlier recognized in DNA-DNA homology studies.
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Hanseniaspora species are widespread and frequent in the environment, mostly studied with respect to their occurrence on grapes and winemaking, and their antagonistic activity against green mould of citrus or B. cinerea has been shown.
“Hanseniaspora species are widespread and frequent in the environment, mostly studied with respect to their occurrence on grapes and winemaking, and their antagonistic activity against green mould of citrus or B. cinerea was shown [78–82].”
From Competition assays and physiological experiments of soil and phyllosphere yeasts identify Candida subhashii as a novel antagonist of filamentous fungi (2017) · cites this paper as [82]
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Hilber-Bodmer, M., Schmid, M., Ahrens, C. H., & Freimoser, F. M. (2017) · BMC Microbiology · doi:10.1186/s12866-016-0908-z · Cited by 106
Metadata
- Authors
- Cadez, N., Raspor, P., Cock, A. W. A. M., Boekhout, T., & Smith, M. T.
- Affiliations
- University of Ljubljana (SI)
- Westerdijk Fungal Biodiversity Institute (NL)
- Venue
- FEMS Yeast Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2002-01
- Volume
- 1
- Issue
- 4
- Pages
- 279-289
- ISSN
- 1567-1356 (ISSN-L)
- 1567-1364
- OpenAlex
- W2103713935
- Cited by
- 71
- References
- 0
- Citations by year
- 2026: 1 · 2023: 1 · 2021: 3 · 2020: 4 · 2019: 5 · 2018: 3 · 2017: 6 · 2016: 3 · 2015: 6 · 2014: 3 · 2013: 2 · 2012: 2
- FWCI
- 1.04
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- FEMS Yeast Research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Microbiology › Yeasts and Rust Fungi Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Pathogens and Fungal Diseases
- Keywords
- Hanseniaspora, Kloeckera, yeast identification, genetic diversity, ITS region, PCR-RFLP, electrophoretic karyotyping, RAPD-PCR, chromosomal polymorphism, microsatellite primers, clustering
- MeSH terms
- Animals, Ascomycota, DNA, Fungal, DNA, Ribosomal, Saccharomycetales, Humans, Karyotyping, Polymorphism, Restriction Fragment Length, Species Specificity, Genetic Variation, Deoxyribonucleases, Type II Site-Specific, Electrophoresis, Gel, Pulsed-Field, Mycological Typing Techniques, Random Amplified Polymorphic DNA Technique
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