نتایج جستجو برای: s rrna 16

تعداد نتایج: 1031043  

Journal: :Nucleic acids research 1984
H Fujiwara T Ogura N Takada N Miyajima H Ishikawa H Maekawa

We obtained two different clones (16 kb and 13 kb) of B. mori rDNA with intron sequence within the 28S-rRNA coding region. The sequence surrounding the intron was found to be highly conserved as indicated in several eukaryotes (Tetrahymena, Drosophila and Xenopus). The 28S rRNA-coding sequence of 16 kb and 13 kb clone was interrupted at precisely the same sites as those where the D. melanogaste...

2017
M. Colby Hunter Alex E. Pozhitkov Peter A. Noble

This article provides supporting data for the research article 'Microbial Signatures of Oral Dysbiosis, Periodontitis and Edentulism Revealed by Gene Meter Methodology' (M.C. Hunter, A.E. Pozhitkov, P.A. Noble, 2016) [1]. In that article, we determined the microbial abundance signatures for patient with periodontics, edentulism, or health using Gene Meter Technology. Here we provide the data us...

2005
Catherine M. BOWMAN

A species of low-molecular-weight ribosomal RNA, referred to as '4.5 S rRNA', was found in addition to 5 S rRNA in the large subunit of chloroplast ribosomes of a wide range of flowering plants. It was shown by sequence analysis that several variants of this RNA may occur in a plant. Furthermore, although in most flowering plants the predominant variant contains about 100 nucleotides, in the br...

2012
Rodrigo Buzinaro Suzuki Cristiane Maria Almeida Márcia Aparecida Sperança

BACKGROUND Treatment effectiveness of Helicobacter pylori varies regionally and is decreasing worldwide, principally as a result of antibiotic resistant bacterium. Tetracycline is generally included in second line H. pylori eradication regimens. In Brazil, a high level of tetracycline resistance (TetR) is mainly associated with AGA926-928TTC 16 S rDNA nucleotide substitutions. As H. pylori cult...

Journal: :Systematic and applied microbiology 2007
Samina Mehnaz Brian Weselowski George Lazarovits

A free-living Gram-negative bacterial strain CR11(T) was isolated from corn roots. Polyphasic taxonomy was performed, including API20 NE and API50 CH bacterial identification kits, Biolog analysis, lipids and fatty acid analysis, DNA-DNA hybridization, 16S rRNA and cpn60 gene sequence analyses. 16S rRNA gene sequence analysis indicated that strain CR11(T) belonged to the genus Sphingobacterium ...

پروبیوتیک­ها به­عنوان استراتژی کنترل‌ زیستی پاتوژن‌های گوارشی مشترک منقله از غذا در ارتقاء امنیت غذایی مصرف کننده مورد توجه هستند. هدف از این پژوهش بررسی خصوصیات پروبیوتیکی و توانایی مهار پاتوژن‌های گوارشی منتقله از غذا توسط باکتری­های اسید لاکتیکی جدا­سازی شده از مجرای گوارش مرغ­های بومی بود. در این مطالعه توانایی تحمل اسید و صفرا در 216 جدایه اسید لاکتیکی بررسی گردید و 13 جدایه برتر به­منظور ...

Journal: :Journal of bacteriology 2009
P P Dennis M Ehrenberg D Fange H Bremer

The value of the rRNA chain elongation rate in bacteria is an important physiological parameter, as it affects not only the rRNA promoter activity but also the free-RNA polymerase concentration and thereby the transcription of all genes. On average, rRNA chains elongate at a rate of 80 to 90 nucleotides (nt) per s, and the transcription of an entire rrn operon takes about 60 s (at 37 degrees C)...

Journal: :The Journal of biological chemistry 2003
Toshiya Hayano Mitsuaki Yanagida Yoshio Yamauchi Takashi Shinkawa Toshiaki Isobe Nobuhiro Takahashi

Nop56p is a component of the box C/D small nucleolar ribonucleoprotein complexes that direct 2'-O-methylation of pre-rRNA during its maturation. Genetic analyses in yeast have shown that Nop56p plays important roles in the early steps of pre-rRNA processing. However, its precise function remains elusive, especially in higher eukaryotes. Here we describe the proteomic characterization of human N...

Journal: :Journal of bacteriology 1993
C J Green B S Vold

The polymerase chain reaction (PCR) was used to detect large tRNA gene clusters in Bacillus subtilis, Bacillus badius, Bacillus megaterium, Lactobacillus brevis, Lactobacillus casei, and Staphylococcus aureus. The primers were based on conserved sequences of known gram-positive bacterial tRNA(Arg) and tRNA(Phe) genes. This PCR procedure detected an unusually large tRNA gene cluster in S. aureus...

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