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1.
Syst Appl Microbiol ; 30(3): 171-9, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16971080

RESUMO

A total of 22 genes from the genome of Salinibacter ruber strain M31 were selected in order to study the phylogenetic position of this species based on protein alignments. The selection of the genes was based on their essential function for the organism, dispersion within the genome, and sufficient informative length of the final alignment. For each gene, an individual phylogenetic analysis was performed and compared with the resulting tree based on the concatenation of the 22 genes, which rendered a single alignment of 10,757 homologous positions. In addition to the manually chosen genes, an automatically selected data set of 74 orthologous genes was used to reconstruct a tree based on 17,149 homologous positions. Although single genes supported different topologies, the tree topology of both concatenated data sets was shown to be identical to that previously observed based on small subunit (SSU) rRNA gene analysis, in which S. ruber was placed together with Bacteroidetes. In both concatenated data sets the bootstrap was very high, but an analysis with a gradually lower number of genes indicated that the bootstrap was greatly reduced with less than 12 genes. The results indicate that tree reconstructions based on concatenating large numbers of protein coding genes seem to produce tree topologies with similar resolution to that of the single 16S rRNA gene trees. For classification purposes, 16S rRNA gene analysis may remain as the most pragmatic approach to infer genealogic relationships.


Assuntos
Proteínas de Bactérias/genética , Bacteroidetes/classificação , Filogenia , Algoritmos , Bacteroidetes/genética , DNA Ribossômico/genética , Evolução Molecular , Funções Verossimilhança , RNA Ribossômico 16S/genética , Alinhamento de Sequência , Análise de Sequência de Proteína
2.
Syst Appl Microbiol ; 29(5): 422-30, 2006 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16337764

RESUMO

Strain OX1 exhibits important physiological, ecological, and biotechnological properties in the degradation of chemical pollutants. It was previously classified as a member of Pseudomonas stutzeri based on its phenotypic characteristics. The present taxonomic study describes phenotypic and genomic properties of strain OX1 and illustrates the value both of multigenic sequence analysis and siderotyping methods to justify its species circumscription within the genus Pseudomonas. We have concluded that strain OX1 is a member of the Pseudomonas corrugata group, distantly related to P. stutzeri, and should be considered representative of a new species. However, phenotypic differentiation between species in this group remains difficult, and species proposals based on only a single strain must be cautious. We, therefore, prefer not to propose a new species until more strains with the same genomic and phenotypic properties as strain OX1 have been isolated.


Assuntos
Pseudomonas/genética , Pseudomonas/metabolismo , Proteínas de Bactérias/genética , DNA Girase/genética , Genótipo , Dados de Sequência Molecular , Fenótipo , Filogenia , Doenças das Plantas/microbiologia , Pseudomonas/classificação , Pseudomonas/patogenicidade
3.
ISME J ; 2(3): 242-53, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18239610

RESUMO

The biogeography of prokaryotes and the effect of geographical barriers as evolutionary constraints are currently subjected to great debate. Some clear-cut evidence for geographic isolation has been obtained by genetic methods but, in many cases, the markers used are too coarse to reveal subtle biogeographical trends. Contrary to eukaryotic microorganisms, phenotypic evidence for allopatric segregation in prokaryotes has never been found. Here we present, for the first time, a metabolomic approach based on ultrahigh resolution mass spectrometry to reveal phenotypic biogeographical discrimination. We demonstrate that strains of the cosmopolitan extremophilic bacterium Salinibacter ruber, isolated from different sites in the world, can be distinguished by means of characteristic metabolites, and that these differences can be correlated to their geographical isolation site distances. The approach allows distinct degrees of discrimination for isolates at different geographical scales. In all cases, the discriminative metabolite patterns were quantitative rather than qualitative, which may be an indication of geographically distinct transcriptional or posttranscriptional regulations.


Assuntos
Bacteroidetes/classificação , Bacteroidetes/metabolismo , Geografia , Sedimentos Geológicos/microbiologia , Cloreto de Sódio , Oceano Atlântico , Proteínas de Bactérias/genética , Bacteroidetes/isolamento & purificação , Bacteroidetes/fisiologia , Espectrometria de Massas , Região do Mediterrâneo , Dados de Sequência Molecular , Peru , Fenótipo , Filogenia , Análise de Sequência de DNA
4.
Int J Syst Evol Microbiol ; 56(Pt 7): 1685-1691, 2006 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16825651

RESUMO

Six strains of extremely halophilic bacteria were isolated from several crystallizer ponds of the Maras solar salterns in the Peruvian Andes. On the basis of 16S rRNA gene sequence similarity, G+C contents and DNA-DNA hybridization results, the six isolates constituted a genomically homogeneous group affiliated with the Gammaproteobacteria. The closest relatives were members of the halophilic genera Halovibrio and Halospina, which showed 16S rRNA gene sequence similarities below 97 % and whole-genome hybridization levels below 33 % for the type strain, 7Sm5(T). From the genomic and phenotypic properties of the six novel isolates and phylogenetic reconstruction based on 16S rRNA gene sequence analysis, they can be considered to represent a novel genus within the Gammaproteobacteria. On the basis of the taxonomic study, a novel genus, Salicola gen. nov., is proposed containing the single species Salicola marasensis sp. nov., which is the type species. The type strain of Salicola marasensis is 7Sm5(T) (=CECT 7107(T)=CIP 108835(T)).


Assuntos
Gammaproteobacteria/classificação , Gammaproteobacteria/isolamento & purificação , Cloreto de Sódio/análise , Microbiologia da Água , Técnicas de Tipagem Bacteriana , Composição de Bases , DNA Bacteriano/química , DNA Bacteriano/genética , DNA Ribossômico/química , DNA Ribossômico/genética , Ácidos Graxos/análise , Ácidos Graxos/química , Gammaproteobacteria/genética , Gammaproteobacteria/fisiologia , Genes de RNAr , Concentração de Íons de Hidrogênio , Dados de Sequência Molecular , Hibridização de Ácido Nucleico , Peru , Filogenia , RNA Bacteriano/genética , RNA Ribossômico 16S/genética , Análise de Sequência de DNA , Homologia de Sequência do Ácido Nucleico , Cloreto de Sódio/farmacologia
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