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  • 16S rRNA cataloguing  (2)
  • 16S rRNA oligonucleotide cataloguing  (1)
  • 1
    ISSN: 1432-072X
    Keywords: Gemmobacter gen. nov. ; Gemmobacter aquatilis sp. nov. ; Blastobacter ; Blastobacter aggregatus ; Phylogeny ; Taxonomy ; 16S rRNA cataloguing ; Fatty acids ; Plasmids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Blastobacter aggregatus and a Blastobacter-like isolate (IFAM 1031) were analysed by the 16S ribosomal RNA cataloguing approach in order to determine their phylogenetic position. Both phenotypical similar organisms are members of the alpha-subdivision of purple phototrophic bacteria and their non-phototrophic relatives but they are not closely related: B. aggregatus clusters with Agrobacterium tumefaciens and Rhizobium species; the unnamed strain displays a moderate relationship to members of Rhodobacter and Paracoccus denitrificans, with which is shares the character of a nicked 23S rRNA. Although the budding isolate IFAM 1031 resembles members of Blastobacter phenotypically, in the broad DNA G+C content and in the fatty acid pattern, a unique set of characters was found which allows description of the isolate as the typus of a new genus for which Gemmobacter gen. nov. is proposed, with G. aquatilis sp. nov. as the type species. G. aquatilis harbors at least two plasmids of different size and unknown function.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 150 (1988), S. 244-248 
    ISSN: 1432-072X
    Keywords: Origin of plastids ; Endosymbiosis ; Chrysophytes (Ochromonas danica) ; Heliobacterium chlorum ; 16S rRNA oligonucleotide cataloguing ; Reverse transcriptase sequencing ; Phylogenetic relations (Molecular phylogeny) ; Chloroplast evolution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The phylogenetic position of the golden-yellow alga Ochromonas danica chrysoplast was investigated by comparison of the 16S rRNA catalogue and two long 16S rRNA stretches (804 and 454 bases) with catalogues from eubacteria and chloroplasts and with homologoes 16S rRNA regions from Escherichia coli, Bacillus subtilis, Heliobacterium chlorum, Anacystis nidulans and chloroplasts from Zea mays, Nicotiana tabacum, Euglena gracilis and Chlamydomonas reinhardii, respectively. Both approaches indicate a closer relationship of the chrysoplast to chloroplasts and cyanobacteria than to the brownish photoheterotrophic Heliobacterium chlorum for which a common ancestry has recently been hypothesized.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-072X
    Keywords: Evolution ; Nif genes ; Nitrogen fixation ; Nitrogenase ; Nucleotide sequence ; Phylogeny ; Rhizobium ; 16S rRNA cataloguing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract It was known that nitrogenase genes and proteins are well conserved even though they are present in a large variety of phylogenetically diverse nitrogen fixing bacteria. This has lead to the speculation, among others, that nitrogen fixation (nif) genes were spread by lateral gene transfer relatively late in evolution. Here we report an attempt to test this hypothesis. We had previously established the complete nucleotide sequences of the three nitrogenase genes from Bradyrhizobium japonicum, and have now analyzed their homologies (or the amino acid sequence homologies of their gene products) with corresponding genes (and proteins) from other nitrogen fixing bacteria. There was a considerable sequence conservation which certainly reflects the strict structural requirements of the nitrogenase iron-sulfur proteins for catalytic functioning. Despite this, the sequences were divergent enough to classify them into an evolutionary scheme that was conceptually not different from the phylogenetic positions, based on 16S rRNA homology, of the species or genera harboring these genes. Only the relation of nif genes of slow-growing rhizobia (to which B. japonicum belongs) and fast-growing rhizobia was unexpectedly distant. We have, therefore, performed oligonucleotide cataloguing of their 16S rRNA, and found that there was indeed only a similarity of S AB=0.53 between fast- and slowgrowing rhizobia. In conclusion, the results suggest that nif genes may have evolved to a large degree in a similar fashion as the bacteria which carry them. This interpretation would speak against the idea of a recent lateral distribution of nif genes among microorganisms.
    Type of Medium: Electronic Resource
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