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1.
Yeungnam University Journal of Medicine ; : 1-10, 2002.
Artigo em Coreano | WPRIM | ID: wpr-140527

RESUMO

With the establishment of rapid sequence analysis of 16S rRNA and the recognition of its patential to determine the phylogenetic position of any prokaryotic organism, the role of 16S rRNA similarities in the present species definition in bacteriology need to be clarified. Comparative studies clearly reveal the limitations of the sequence analysis of this conserved gene and gene product in the determination of relationship at the pathogenic strain level for which DNA-DNA reassociation exprements still constitute the superior method. Since today the primary structure of 16S rRNA is easier to determine than hybridization between DNA strands, the strength of the sequence analysis is to recognize the level at which DNA pairing studies need to be performed, which certainly applies to similarities of 97% and higher.


Assuntos
Bacteriologia , DNA , Genoma Microbiano , Análise de Sequência
2.
Yeungnam University Journal of Medicine ; : 1-10, 2002.
Artigo em Coreano | WPRIM | ID: wpr-140526

RESUMO

With the establishment of rapid sequence analysis of 16S rRNA and the recognition of its patential to determine the phylogenetic position of any prokaryotic organism, the role of 16S rRNA similarities in the present species definition in bacteriology need to be clarified. Comparative studies clearly reveal the limitations of the sequence analysis of this conserved gene and gene product in the determination of relationship at the pathogenic strain level for which DNA-DNA reassociation exprements still constitute the superior method. Since today the primary structure of 16S rRNA is easier to determine than hybridization between DNA strands, the strength of the sequence analysis is to recognize the level at which DNA pairing studies need to be performed, which certainly applies to similarities of 97% and higher.


Assuntos
Bacteriologia , DNA , Genoma Microbiano , Análise de Sequência
3.
J Biosci ; 1984 Dec; 6(6): 817-821
Artigo em Inglês | IMSEAR | ID: sea-160425

RESUMO

The utility of formamide in the denaturation and renaturation of DNA has been examined. The melting temperature of duplex DNA is lowered by 0·6oC per per cent formamide. The depression of melting temperature is independent of the GC content. Formamide also increases the width of the thermal transition. Upto 30%, it does not affect the rate of DNA reassociation.

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