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Braz. j. med. biol. res ; 37(12): 1763-1769, Dec. 2004. tab, graf
Article Dans Anglais | LILACS | ID: lil-388059

Résumé

The histone-like protein H1 (H-NS) is an abundant structural component of the bacterial nucleoid and influences many cellular processes including recombination, transcription and transposition. Mutations in the hns gene encoding H-NS are highly pleiotropic, affecting the expression of many unrelated genes. We have studied the role of H-NS on the regulation of hemolysin gene expression in Serratia marcescens. The Escherichia coli hns mutant carrying S. marcescens hemolysin genes on a plasmid constructed by ligation of the 3.2-kb HindIII-SacI fragment of pR02 into pBluescriptIIKS, showed a high level of expression of this hemolytic factor. To determine the osmoregulation of wild-type and hns defective mutants the cells were grown to mid-logarithmic phase in LB medium with 0.06 or 0.3 M NaCl containing ampicillin and kanamycin, whereas to analyze the effect of pH on hemolysin expression, the cells were grown to late-logarithmic phase in LB medium buffered with 0.1 M Tris-HCl, pH 4.5 to 8.0. To assay growth phase-related hemolysin production, bacterial cells were grown in LB medium supplemented with ampicillin and kanamycin. The expression of S. marcescens hemolysin genes in wild-type E. coli and in an hns-defective derivative at different pH and during different growth phases indicated that, in the absence of H-NS, the expression of hemolysin did not vary with pH changes or growth phases. Furthermore, the data suggest that H-NS may play an important role in the regulation of hemolysin expression in S. marcescens and its effect may be due to changes in DNA topology influencing transcription and thus the amount of hemolysin expression. Implications for the mechanism by which H-NS influences gene expression are discussed.


Sujets)
Protéines bactériennes/physiologie , Protéines de liaison à l'ADN/physiologie , Régulation de l'expression des gènes bactériens/génétique , Hémolysines/génétique , Serratia marcescens/génétique , Protéines bactériennes/génétique , Milieux de culture , Protéines de liaison à l'ADN/génétique , Escherichia coli/génétique , Génotype , Régulation de l'expression des gènes bactériens/physiologie , Concentration en ions d'hydrogène , Hémolysines/biosynthèse , Mutation , Serratia marcescens/métabolisme
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