نتایج جستجو برای: 23s rdna

تعداد نتایج: 13732  

2016
Shutu Xu Qianqian Sun Xiaohua Zhou Xiao Tan Man Xiao Wei Zhu Ming Li

The 16S rDNA, 16S-23S rDNA-ITS, cpcBA-IGS, mcy gene and several polysaccharide biosynthesis-related genes (epsL and TagH) were analyzed along with the identification of the morphology of Microcystis colonies collected in Lake Taihu in 2014. M. wesenbergii colonies could be distinguished directly from other colonies using espL. TagH divided all of the samples into two clusters but failed to dist...

Journal: :European heart journal 2010
Tanja Vollmer Cornelia Piper Dieter Horstkotte Reiner Körfer Knut Kleesiek Jens Dreier

AIMS A new diagnostic strategy to improve the detection of pathogens in heart valves (HVs) from patients with infective endocarditis (IE) was evaluated. METHODS AND RESULTS Three hundred and fifty seven HVs surgically removed from 326 patients with proven IE or suspicious intra-operative findings, examined by 16S rDNA polymerase chain reaction (PCR) and culture were retrospectively analysed a...

2012
Hasan Shojaei Hashemi Abodolrazagh Parvin Heidarieh Fazel Pourahmad Daei Naser Daei Naser

OBJECTIVES In addition to several molecular methods and in particular 16S rDNA analysis, the application of a more discriminatory genetic marker, i.e., 16S-23S internal transcribed spacer gene sequence has had a great impact on identification and classification of mycobacteria. In the current study we aimed to apply this sequencing power to conclusive identification of some Iranian clinical str...

2013
Vijai Singh Indra Mani Dharmendra Kumar Chaudhary

Aeromonas hydrophila is an important bacterial pathogen which causes the hemorrhagic septicemia in fishes, amphibians and humans. Genetic relationships of diverse isolates of A. hydrophila were recovered from fish and water sources. These isolates were investigated by flanked region of 16S and 23S Ribosomal DNA (rDNA) internal transcribed spacer (ITS). Here we analyzed polymorphism of PCR-ampli...

2007
Jennifer HODGETTS Nigel HARRISON Rick MUMFORD Neil BOONHAM Matt DICKINSON

Phylogenetic analysis of a 500 bp fragment of the secA gene has been performed on 35 phytoplasma isolates representing 10 of the 16S rDNA groups. The lineages obtained coincide with those delineated by 16S rDNA phylogenetic analysis but much greater genetic variability was evident. In addition, phylogenetic analysis based on part of the 23S rDNA gene combined with T-RFLP (terminal restriction f...

Journal: :Nucleic acids research 1999
D Ammons J Rampersad G E Fox

In Escherichia coli, ribosomal RNAs (16S, 23S and 5S) are co-transcribed in a highly regulated manner from seven genomically dispersed operons. Previous studies on the cellular effects of altered levels of two of these rRNAs (16S and 23S) have been useful in better understanding the regulation of rRNA expression. Furthering these studies, we have investigated the effect of 5S rRNA deficiencies ...

Journal: :Applied and environmental microbiology 1998
Khbaya Neyra Normand Zerhari Filali-Maltouf

Forty rhizobia nodulating four Acacia species (A. gummifera, A. raddiana, A. cyanophylla, and A. horrida) were isolated from different sites in Morocco. These rhizobia were compared by analyzing both the 16S rRNA gene (rDNA) and the 16S-23S rRNA spacer by PCR with restriction fragment length polymorphism (RFLP) analysis. Analysis of the length of 16S-23S spacer showed a considerable diversity w...

2005
José M. Igual Angel Valverde Encarna Velázquez Ignacio Santa Regina

15 The genetic diversity of Frankia strains nodulating Alnus glutinosa along the basin of the Tormes River was 16 studied on DNA extracted directly from nodules. Frankia strains inhabiting root nodules at 12 different 17 locations, ranging in altitude from 409 to 1181 m, were characterized. For that, we amplified the whole IGS 18 region between 16S–23S rDNA and performed a restriction fragment ...

ژورنال: دنیای میکروب ها 2009
انیس جعفری عباس دوستی, میثم سرشار نادر شاهرخی,

سابقه و هدف: روش های سنتی در تشخیص باکتری های پاتوژن منتقله از طریق غذا بسیار وقت گیر و زمانبر می باشند، بنابراین استفاده از روش های دقیق و قابل اطمینان در تشخیص پاتوژن های میکروبی مورد نیاز است. هدف از این پژوهش طراحی پرایمرهای یونیورسال برای تکثیر ژن 23S rDNA و هیبریدیزاسیون ریز آرایه های الیگونوکلئوتیدی به منظور ارزیابی کارایی و عملکرد توالی 23S rDNA در تشخیص باکتر...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید