نتایج جستجو برای: 16s rdna pcr
تعداد نتایج: 199975 فیلتر نتایج به سال:
A study of 59 isolates of Bartonella henselae reveals relatively limited diversity among those of human origin (n = 28). Either of two distinct alleles of both gltA and 16S ribosomal DNA (rDNA) was found in all isolates, with a high level of congruity between 16S and gltA inheritance among proven human pathogens. Human isolates from all over Eastern Australia were most commonly 16S rDNA (Bergma...
Microbial ecologists have discovered novel rRNA genes (rDNA) in mesophilic soil habitats worldwide, including sequences that affiliate phylogenetically within the division Crenarchaeota (domain Archaea). To characterize the spatial distribution of crenarchaeal assemblages in mesophilic soil habitats, we profiled amplified crenarchaeal 16S rDNA sequences from diverse soil ecosystems by using PCR...
زمینه و هدف: پروبیوتیک ها میکروارگانیسم های غیر پاتوژن و مفیدی هستند که شناسایی آنها در محصولات لبنی سنتی نه تنها میتواند منجر به جداسازی باکتریهای پروبیوتیکی با خصوصیات ویژه شود، بلکه میتواند دیدگاه مناسبی برای تولید انبوه محصولات لبنی سنتی که به طور طبیعی حاوی باکتریهای پروبیوتیکی هستند به ما عرضه کند. مواد و روش ها: پس از نمونه برداری محصولات لبنی از مناطق مختلف شهرستان، کشتهای متوالی...
Human colonic biota is a complex microbial ecosystem that serves as a host defense. Unlike most microbial ecosystems, its composition has been studied extensively by relatively efficient culture methods. We have compared an established culture-based method with direct amplification and partial sequencing of cloned 16S rRNA genes from a human fecal specimen. Nine cycles of PCR were also compared...
In the present study, we aimed to develop a nucleic acid lateral-flow method for the rapid and sensitive detection of multiple bacteria that contaminate platelet concentrations (PCs). Polymerase chain reaction (PCR) amplicons were produced by a set of board-range primers that recognize the conserved region of bacteria 16S rDNA, followed by hybridization with both an FITC (fluorescein isothiocy...
AIM Rapid detection of H.pylori strains by PCR-Sequencing. METHODS 16S rDNA amplification by PCR from template genomic DNA, confirmation of amplicon size by agarose gel electrophoresis, sequencing of amplicons by automated sequencer, analysis of sequences by NCBI -BLAST software. RESULTS The PCR -Sequencing and analysis of the sequence data by BLAST resulted in detection of the strain to be...
مقدمه: باکتری های اندوفیت با توانائی تولید ترکیبات آنتاگونیست، قادر به کنترل بیمارگرهای گیاهی هستند. این مطالعه به منظور بررسی توانایی تولید ترکیبات آنتاگونیستی در باکتری های اندوفیت برگ نو انجام پذیرفته است. مواد و روش ها: در این پژوهش باکتری های اندوفیت از برگ و شاخه برگ نو، جداسازی گردید، پس از استخراج DNA ژنومی، از روش PCR به منظور تکثیر ژن 16S rDNA استفاده گردید. به منظور شناسایی دقیق ...
Nitrate reduction is performed by phylogenetically diverse bacteria. Analysis of narG (alpha subunit of the membrane bound nitrate reductase) trees constructed using environmental sequences revealed a new cluster that is not related to narG gene from known nitrate-reducing bacteria. In this study, primers targeting this as yet uncultivated nitrate-reducing group were designed and used to develo...
Polymicrobial biofilms in the human oral cavity exhibit marked diversity. PCR-based denaturing gradient gel electrophoresis (PCR-DGGE) surveys microbial diversity by displaying PCR-generated 16S rDNA fragments that migrate at different distances, reflecting the differences in the base-pair (i.e., % G+C) composition of the fragment. This study examined DGGE-generated diversity profiles of cultiv...
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