نتایج جستجو برای: 16s rrna genes

تعداد نتایج: 453468  

2009
Zarraz May-Ping Lee Carl Bussema Thomas M. Schmidt

A dramatic exception to the general pattern of single-copy genes in bacterial and archaeal genomes is the presence of 1-15 copies of each ribosomal RNA encoding gene. The original version of the Ribosomal RNA Database (rrnDB) cataloged estimates of the number of 16S rRNA-encoding genes; the database now includes the number of genes encoding each of the rRNAs (5S, 16S and 23S), an internally tra...

Journal: :Journal of clinical microbiology 2011
Michinori Funato Hideo Kaneko Kiyofumi Ohkusu Hideo Sasai Kazuo Kubota Hidenori Ohnishi Zenichiro Kato Toshiyuki Fukao Naomi Kondo

We describe a 35-year-old man with X-linked agammaglobulinemia who had refractory chronic pleurisy caused by a Helicobacter equorum-like bacterium. Broad-range bacterial PCR targeting the 16S and 23S rRNA genes and in situ hybridization targeting the 16S rRNA gene of H. equorum confirmed the presence of this pathogen in a human for the first time.

Journal: :Applied and environmental microbiology 1998
J R Marchesi T Sato A J Weightman T A Martin J C Fry S J Hiom D Dymock W G Wade

We report the design and evaluation of PCR primers 63f and 1387r for amplification of 16S rRNA genes from bacteria. Their specificity and efficacy were tested systematically with a bacterial species and environmental samples. They were found to be more useful for 16S rRNA gene amplification in ecological and systematic studies than PCR amplimers that are currently more generally used.

Journal: :Applied and environmental microbiology 2004
Gordon Webster R John Parkes John C Fry Andrew J Weightman

Phylogenetic analysis of 16S rRNA gene sequences from deep marine sediments identified a deeply branching clade, designated candidate division JS1. Primers for PCR amplification of partial 16S rRNA genes that target the JS1 division were developed and used to detect JS1 sequences in DNA extracted from various sedimentary environments, including, for the first time, coastal marine and brackish s...

Journal: :Applied and environmental microbiology 2010
Paul W J J van der Wielen Gertjan Medema

Bacteroidales species were detected in (tap) water samples from treatment plants with three different PCR assays. 16S rRNA gene sequence analysis indicated that the sequences had an environmental rather than fecal origin. We conclude that assays for Bacteroidales 16S rRNA genes are not specific enough to discern fecal contamination of drinking water in the Netherlands.

Journal: :Applied and environmental microbiology 2009
Katelyn A Nelson Nicole S Moin Anne E Bernhard

Crenarchaeal 16S rRNA sequences constituted over 70% of the archaeal clones recovered from three salt marsh sites dominated by different grasses. Group I.1a Crenarchaeota dominated at two sites, while group I.3b Crenarchaeota sequences were most abundant at a third site. Abundances of 16S rRNA genes related to "Candidatus Nitrosopumilus maritimus" differed by site and sampling date.

Journal: :International journal of systematic and evolutionary microbiology 2006
Rob U Onyenwoke Yong-Jin Lee Slawomir Dabrowski Birgitte K Ahring Juergen Wiegel

Although the type species of the genus Thermoanaerobium, Thermoanaerobium brockii, was transferred to Thermoanaerobacter, Thermoanaerobium acetigenum was not transferred. Therefore, Thermoanaerobium acetigenum should be reclassified. Based on 16S rRNA gene sequence analysis and re-examination of physiological properties of the type strain, X6B(T) (=DSM 7040(T) = ATCC BAA-1149(T)), we propose th...

2007
Kunikazu Yamane Jun-ichi Wachino Satowa Suzuki Naohiro Shibata Haru Kato Keigo Shibayama Kouji Kimura Kumiko Kai Satoshi Ishikawa Yoshiyuki Ozawa Toshifumi Konda Yoshichika Arakawa

To investigate the exact isolation frequency of 16S rRNA methylase-producing, gram-negative pathogenic bacteria, we tested 87,626 clinical isolates from 169 hospitals. Twenty-six strains from 16 hospitals harbored 16S rRNA methylase genes, which suggests sparse but diffuse spread of pan-aminoglycoside-resistant microbes in Japan.

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