Detection of prokaryotic microbial communities of Çamaltı Saltern, Turkey, by fluorescein in situ hybridization and real-time PCR

Knowledge of the functions, interactions, and diversity of extremely halophilic microorganisms mostly comes from the results of studies performed in different salterns throughout the world. As model habitats, salterns allow the comparison of different techniques used for qualitative and quantitative analysis of halophilic communities in these hypersaline environments. Çamaltı Saltern is the biggest coastal solar saltern located on the Aegean coast of Turkey, and it produces most of the salt consumed in the country. In the present study, detection of prokaryotic communities of the Çamaltı Saltern was performed using 2 culture-independent methods. Real-time polymerase chain reaction (RT-PCR) and fluorescein in situ hybridization (FISH) techniques were evaluated to analyze the microbial populations of Çamaltı Saltern. Of the Çamaltı samples, 48% to 67% were hybridized with the EUB338 probe and 33% to 57% were hybridized with the ARC915 probe. Repeatability of the RT-PCR experiments with environmental DNA was considered insufficient. However, FISH analysis may be combined with RT-PCR and these 2 techniques may be used in tandem to rapidly reveal quantitative aspects of the microbial population of hypersaline environments.

Detection of prokaryotic microbial communities of Çamaltı Saltern, Turkey, by fluorescein in situ hybridization and real-time PCR

Knowledge of the functions, interactions, and diversity of extremely halophilic microorganisms mostly comes from the results of studies performed in different salterns throughout the world. As model habitats, salterns allow the comparison of different techniques used for qualitative and quantitative analysis of halophilic communities in these hypersaline environments. Çamaltı Saltern is the biggest coastal solar saltern located on the Aegean coast of Turkey, and it produces most of the salt consumed in the country. In the present study, detection of prokaryotic communities of the Çamaltı Saltern was performed using 2 culture-independent methods. Real-time polymerase chain reaction (RT-PCR) and fluorescein in situ hybridization (FISH) techniques were evaluated to analyze the microbial populations of Çamaltı Saltern. Of the Çamaltı samples, 48% to 67% were hybridized with the EUB338 probe and 33% to 57% were hybridized with the ARC915 probe. Repeatability of the RT-PCR experiments with environmental DNA was considered insufficient. However, FISH analysis may be combined with RT-PCR and these 2 techniques may be used in tandem to rapidly reveal quantitative aspects of the microbial population of hypersaline environments.

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Turkish Journal of Biology-Cover
  • ISSN: 1300-0152
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

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Production, purification, and characterization of α-amylase by Bacillus subtilis and its mutant derivates

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