2005
DOI: 10.1271/bbb.69.1995
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Paenibacillus maceransPossesses Two Types of 16S rDNA Copies in a Genome with a Length Difference of Twelve Base Pairs

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Cited by 5 publications
(3 citation statements)
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References 12 publications
(13 reference statements)
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“…The cloned 16S rRNA genes revealed three types of sequences in strains B27 T and F6-B70, indicating intra-genomic heterogeneity, which has been found in other species of the genus Paenibacillus (Bosshard et al , 2002; Hamasaki et al , 2005; Nübel et al , 1996; Roux & Raoult, 2004). Comparative 16S rRNA gene sequence analyses showed that strains B27 T and F6-B70 were phylogenetically affiliated to the genus Paenibacillus .…”
mentioning
confidence: 71%
“…The cloned 16S rRNA genes revealed three types of sequences in strains B27 T and F6-B70, indicating intra-genomic heterogeneity, which has been found in other species of the genus Paenibacillus (Bosshard et al , 2002; Hamasaki et al , 2005; Nübel et al , 1996; Roux & Raoult, 2004). Comparative 16S rRNA gene sequence analyses showed that strains B27 T and F6-B70 were phylogenetically affiliated to the genus Paenibacillus .…”
mentioning
confidence: 71%
“…32 Most of these bacteria are found in soil and on plants and are known or presumed to form endospores. 12,16,20,21,26,40,49 In one contamination, we also identified M. luteus, which belongs to the phylum Actinobacteria and is an obligate aerobe associated with soil, plants, and the human skin microbiome. 17 The characteristics of the contaminants do not directly allow reconstruction of the contamination routes, but they suggest that contamination occurred either via surfaces contaminated by contact with human skin (for example, hands) or unclean air or through the introduction of contaminated feed or bedding.…”
Section: Discussionmentioning
confidence: 99%
“…two universal primers each with 0.2 mM concentration, 2.5 U Tay DNA polymerase (Genei, Bangalore), and four deoxynucleoside triphosphate each in 0.2 mM concentration. The primer sequence selection was done from the regions of 16s rDNA and the 16s rDNA was amplified by using universal forward primer 5-TGGAGAGTTTGATCCTGGCTCAG-3' and universal reverse primer 5'-TACCGCGGCTGCTGGCAC-3' (Hamasaki et al, 2005;Hall et al, 2003). After an initial denaturation for 2 min at 95°C, 25 cycles were completed each consisting of Imin at 94C, 50 sec at 60°C annealing temperature, and 1.5min at 72°C.…”
Section: Pcr Amplificationmentioning
confidence: 99%