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1.
Acta Microbiol Immunol Hung ; 50(4): 395-406, 2003.
Article in English | MEDLINE | ID: mdl-14750440

ABSTRACT

Recently developed molecular biology approaches make possible the detailed genetic, taxonomic and ecological examination of microorganisms from various habitats. Animal gut represents one of the most complex microbial ecosystems with a large degree of microbial biodiversity present. Bacteria inhabiting the gut usually play important roles in metabolic transformations of substrates and sometimes, e.g. in ruminants, they make the basis for an obligate symbiosis with the host. Here we discuss molecular microbiology as a strategy for examination of gut bacteria, concentrating on a typical and in such environment dominant group of strictly anaerobic Gram-negative bacteria from the phylogenetic group Cytophaga/Flexibacter/Bacteroides. The bacteria from the genus Prevotella are the most abundant Gram-negative bacteria in the rumen and form a distinctive phylogenetic cluster, clearly separated from prevotellas isolated from other ecological niches. They may represent a good choice for a model organism in genetic manipulation experiments and for studies of gene transfer mechanisms taking place in the gut. The molecular tools for detection and monitoring of ruminal prevotellas are discussed.


Subject(s)
Digestive System/microbiology , Gram-Negative Anaerobic Bacteria/genetics , Gram-Negative Anaerobic Bacteria/isolation & purification , Animals , DNA, Bacterial/genetics , Ecosystem , Genetic Variation , Gram-Negative Anaerobic Bacteria/classification , Humans , Molecular Biology , Phylogeny , Prevotella/genetics , Prevotella/isolation & purification , Rumen/microbiology
2.
Folia Microbiol (Praha) ; 46(1): 33-5, 2001.
Article in English | MEDLINE | ID: mdl-11501472

ABSTRACT

Extracellular non-specific nucleases were observed in some strains belonging to the ruminal species of the genus Prevotella, mostly P. brevis and P. bryantii. The nuclease from P. bryantii appeared to be extracellular; it mediates the degradation of the supercoiled plasmid DNA via an open circle intermediate. The cleavage is not site specific although a preference for certain cleavage sites does seem to exist. Our attempts to clone the wild-type P. bryantii B(1)4 nuclease in E. coli strain ER1992 that reports on the DNA damage sustained, were unsuccessful probably due to excessive intracellular nuclease activity that killed the cells bearing the gene for the nuclease. On the other hand, the nuclease from a related strain TCl-1, which has a less active enzyme of the same type, was successfully cloned.


Subject(s)
Cloning, Molecular , Deoxyribonucleases/genetics , Deoxyribonucleases/metabolism , Prevotella/enzymology , Rumen/microbiology , Animals , DNA, Bacterial/metabolism , Escherichia coli/enzymology , Escherichia coli/genetics , Plasmids/genetics , Prevotella/genetics
3.
Folia Microbiol (Praha) ; 46(1): 91-3, 2001.
Article in English | MEDLINE | ID: mdl-11501488

ABSTRACT

A new spirochetal strain was isolated from the rumen of a black-and-white Holstein cow and preliminarily characterized. The sugar fermentation tests and morphological observations indicated this organism to be a member of a novel, as yet undescribed spirochetal rumen species. The small subunit ribosomal RNA genes were amplified and the PCR products were cut with the restriction endonucleases TaqI, DdeI, HhaI and Sau3AI. The comparison of the observed RFLP with the hypothetical fragment lengths of the computer analyzed 16S rRNA sequences from the type strains of the ruminal spirochetes Treponema bryantii and T. saccharophilum confirmed the tentative novel identification. Transmission electron microscopy showed that the bacterium has the typical spirochetal structures, i.e. the outer sheath, the protoplasmic cylinder and the axial filament (it is not yet clear how many flagella compose the filament). An additional extracellular structure was observed which appeared as an exocytoplasmic polar flagellum, approximately 2 microns long and protruding from one tip of the cell. The average size of the cells was 0.5 x 10-15 microns and the wavelengths and the amplitudes of the primary coils were 2.9 and 1.3 microns, respectively.


Subject(s)
Rumen/microbiology , Treponema/classification , Treponema/genetics , Animals , Cattle , Culture Media , DNA, Bacterial/analysis , DNA, Bacterial/genetics , Fermentation , Genes, rRNA , Microscopy, Electron , Polymorphism, Restriction Fragment Length , RNA, Ribosomal, 16S/genetics , RNA, Ribosomal, 16S/metabolism , Treponema/isolation & purification
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