1997
DOI: 10.1016/s0168-1605(97)88066-x
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Development of oligonucleotide primers from the 16S-23S rRNA intergenic sequences for identifying different dairy and probiotic lactic acid bacteria by PCR

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Cited by 210 publications
(110 citation statements)
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“…The authenticity of the strains was checked by a 259-bp PCR amplification product of the 16S-23S rRNA gene spacer region using the species-specific primer pair ThI and ThII (23). The PCR amplification profile was used as described by Tilsala-Timisjärvi et al (23).…”
Section: Methodsmentioning
confidence: 99%
“…The authenticity of the strains was checked by a 259-bp PCR amplification product of the 16S-23S rRNA gene spacer region using the species-specific primer pair ThI and ThII (23). The PCR amplification profile was used as described by Tilsala-Timisjärvi et al (23).…”
Section: Methodsmentioning
confidence: 99%
“…In particular, the comparison of the sequences of the gene 16S of the ribosomal RNA (rRNA) is one of the most powerful and efficient techniques for the determination of the phylogenetic degree of relatedness among microorganisms (Woese, 1987). Therefore, the sequencing of the gene that codifies the 16S rRNA and the sequencing of the intergenic region is a technique that has been increasingly used to characterize the microbial diversity of food, including dairy products (Guedes Neto, 2008;Tilsala-Timisjärvi & Alatossava, 1997).…”
Section: Introductionmentioning
confidence: 99%
“…Recently, length and sequence polymorphisms in the spacers within the rrn loci have been used to discriminate between species of lactobacilli, as well as to identify different dairy and probiotic lactic acid bacteria (Tilsala-Timisjarvi & Alatossava, 1997 ;Nakagawa et al, 1994). However, the data available on the ISRs of lactobacilli are not sufficient and all the previous studies targeted the 16S-23S rRNA ISRs.…”
Section: Introductionmentioning
confidence: 99%