Results 71 to 80 of about 505,000 (387)
PCR primers to amplify 16S rRNA genes from cyanobacteria [PDF]
Applied and Environmental Microbiology, 1997 We developed and tested a set of oligonucleotide primers for the specific amplification of 16S rRNA gene segments from cyanobacteria and plastids by PCR. PCR products were recovered from all cultures of cyanobacteria and diatoms that were checked but not from other bacteria and archaea. Gene segments selectively retrieved from cyanobacteria and diatoms
Nübel, U. +2 more
openaire +3 more sources
International Journal of Mycobacteriology, 2012 Background: Conventional biochemical tests are the standard for the identification of Mycobacterium species, but molecular identifications are becoming more prevalent.
Yuko Kazumi, Satoshi Mitarai
doaj +1 more source
Инфекция и иммунитет, 2022 Introduction. Sequencing of the 16S rRNA gene is the predominant method for assessing microbial communities and strain molecular identification. The short reads (2nd generation sequencing)-based technology does not allow analysis beyond the 16S rRNA gene.
O. B. Ogarkov +6 more
doaj +1 more source
Characterization of Francisella species isolated from the cooling water of an air conditioning system. [PDF]
, 2015 Strains of Francisella spp. were isolated from cooling water from an air conditioning system in Guangzhou, China. These strains are Gram negative, coccobacilli, non-motile, oxidase negative, catalase negative, esterase and lipid esterase positive.
Atwill, Edward +6 more
core +3 more sources
Microbiome, 2014 To take advantage of affordable high-throughput next-generation sequencing technologies to characterize microbial community composition often requires the development of improved methods to overcome technical limitations inherent to the sequencing ...
D. Fadrosh +6 more
semanticscholar +1 more source
Two different 16S rRNA genes in a mycobacterial strain [PDF]
Journal of Clinical Microbiology, 1996 Sequencing of the gene coding for 16S rRNA (16S rDNA) is a well-established method used to identify bacteria, particularly mycobacteria. Unique sequences allow identification of a particular genus and species. If more than one 16S rDNA is present on one mycobacterial genome, their sequences are assumed to be strictly or almost identical.
Bescher Ninet, Béatrice Alice +7 more
openaire +3 more sources
Substrate-specific clades of active marine methylotrophs associated with a phytoplankton bloom in a temperate coastal environment [PDF]
, 2008 Marine microorganisms that consume one-carbon (C1) compounds are poorly described, despite their impact on global climate via an influence on aquatic and atmospheric chemistry.
Boden, Rich +4 more
core +2 more sources
Genetic Environment of 16S rRNA Methylase Gene rmtD [PDF]
Antimicrobial Agents and Chemotherapy, 2008 ABSTRACT The genetic environment of the 16S rRNA methylase gene rmtD was investigated. rmtD was flanked by a novel IS CR motif located downstream of class I integron In 163 in the original Pseudomonas aeruginosa
Doi, Y. +2 more
openaire +3 more sources
bioRxiv, 2018 Targeted PCR amplification and high-throughput sequencing (amplicon sequencing) of 16S rRNA gene fragments is widely used to profile microbial communities.
B. Callahan +7 more
semanticscholar +1 more source
Taxonomic and Characterization Methods of Streptomyces: A Review
Progress in Microbes and Molecular Biology, 2018 The 16S ribosomal RNA gene is the gold standard for taxonomic identification and phylogenetic study of most of the bacteria. However, the resolution of 16S rRNA gene is found to be insufficient to distinguish closely related Streptomyces species within ...
Jodi Woan-Fei Law +4 more
doaj +1 more source