2008
DOI: 10.1080/13102818.2008.10817545
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Molecular Typing by Genus-Specific PCR and Rapd Profiling of DiverseLactobacillus DelbrueckiiStrains Isolated from Cow, Sheep and Buffalo Yoghurts

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Cited by 10 publications
(5 citation statements)
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“…These basic phenotypic methods include morphology, Gram staining and biochemical tests such as fermentation of carbohydrates or growth at varying temperatures and salt concentrations [ 12 ]. Morphology screening for differentiation seems problematic, as it is known that lactobacilli have diverse morphotypes within the same species [ 13 ]. Fortunately, for species-specific identification of strains based on physiological properties other modern tools have become available over the last years such as the API system from Biomérieux (France), the Diatabs system (Rosco, Denmark) or the BIOLOG GP MicroPlate System (BIOLOG Inc., USA).…”
Section: Introductionmentioning
confidence: 99%
“…These basic phenotypic methods include morphology, Gram staining and biochemical tests such as fermentation of carbohydrates or growth at varying temperatures and salt concentrations [ 12 ]. Morphology screening for differentiation seems problematic, as it is known that lactobacilli have diverse morphotypes within the same species [ 13 ]. Fortunately, for species-specific identification of strains based on physiological properties other modern tools have become available over the last years such as the API system from Biomérieux (France), the Diatabs system (Rosco, Denmark) or the BIOLOG GP MicroPlate System (BIOLOG Inc., USA).…”
Section: Introductionmentioning
confidence: 99%
“…Sobotka et al (2004) concluded that AFLP method detected polymorphisms in oilseed rape cultivars more efficiently than either RAPD or SSR methods, but also stated the importance to detect informative markers and confirmed that the results obtained by different marker systems were often similar. The main disadvantage of RAPD method is often reported to be a low reproducibility, but improved laboratory techniques and more exact band scoring help upgrading the poor reproducibility in RAPD analyses (Ivanova et al, 2008). Genetic diversity is best estimated if other markers -agro-morphological, biochemical are also studied (Yu et al, 2005;Galović et al, 2006).…”
Section: Introductionmentioning
confidence: 99%
“…The isolates were first identified on the basis of Gram stain, morphology, catalase reaction and advanced biochemical tests. For molecular identification of the bacteria, genomic DNA of the isolates was extracted using a genomic DNA purification kit (Fermentas), and the isolates were identified by primers specific for the 16S rDNA gene sequences (forward 5 0 -TGG AAA CAG RTG CTA ATA CCG-3 0 and reverse 5 0 -GTC CAT TGT GGA AGA TTC CC-3 0 ; Ivanova et al 2008). The 16S rDNA fragment was amplified using HotStarTaq Master Mix (Qiagen, Ankara, Turkey) in a Techne TC-512 thermocycler (Techne, UK) under the following conditions: 94°C for 2 min, 30 cycles of 94°C for 20 s, 59°C for 30 s, 72°C for 1 min and finally 72°C for 5 min.…”
Section: Methodsmentioning
confidence: 99%