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1.
Adv Appl Microbiol ; 52: 29-74, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12964239

RESUMEN

DNA recombinases show some promise as reporters of pollutants providing that appropriate promoters are used and that the apparent dependence of expression on cell density can be solved. Further work is in progress using different recombinases and other promoters to optimize recombinase expression as well as to test these genetic constructs in contaminated environmental samples such as soil and water. It may be that a graded response reflecting pollutant concentration may not be possible. However, they show great promise for providing definitive detection systems for the presence of a pollutant and may be applicable to address the problem of bioavailability of pollutants in complex environments such as soil.


Asunto(s)
Técnicas Biosensibles/métodos , Monitoreo del Ambiente/métodos , Contaminantes Ambientales/análisis , Recombinasas/metabolismo , Microbiología del Suelo , Xenobióticos/metabolismo , Bacterias/metabolismo , Contaminantes Ambientales/metabolismo , Genes Reporteros/fisiología
2.
J Bacteriol ; 187(24): 8256-66, 2005 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-16321930

RESUMEN

The fim genetic switch in the chromosome of Escherichia coli K-12 is an invertible DNA element that harbors the promoter for transcription of the downstream fim structural genes and a transcription terminator that acts on the upstream fimE regulatory gene. Switches oriented appropriately for structural gene transcription also allow fimE mRNA to read through, whereas those in the opposite orientation terminate the fimE message. We show here that termination is Rho dependent and is suppressed in a rho mutant or by bicyclomycin treatment when fimE mRNA is expressed by the fimE gene, either from a multicopy recombinant plasmid or in its native chromosomal location. Two cis-acting elements within the central portion of the 314-bp invertible DNA switch were identified as contributors to Rho-dependent termination and dissected. These fim sequence elements show similarities to well-characterized Rho utilization (rut) sites and consist of a boxA motif and a C-rich and G-poor region of approximately 40 bp. Deletion of the boxA motif alone had only a subtle negative effect on Rho function. However, when this element was deleted in combination with the C-rich, G-poor region, Rho function was considerably decreased. Altering the C-to-G ratio in favor of G in this portion of the switch also strongly attenuated transcription termination. The implications of the existence of a fimE-specific Rho-dependent terminator within the invertible switch are discussed in the context of the fim regulatory circuit.


Asunto(s)
Proteínas de Unión al ADN/genética , Escherichia coli K12/genética , Proteínas de Escherichia coli/genética , Regulación Bacteriana de la Expresión Génica , Factor Rho/fisiología , Regiones Terminadoras Genéticas , Transcripción Genética , Composición de Base/genética , Composición de Base/fisiología , Compuestos Bicíclicos Heterocíclicos con Puentes/farmacología , ADN Bacteriano/genética , ADN Bacteriano/fisiología , Proteínas de Unión al ADN/fisiología , Inhibidores Enzimáticos/farmacología , Proteínas de Escherichia coli/fisiología , Fimbrias Bacterianas/genética , Integrasas/genética , Integrasas/fisiología , Modelos Biológicos , Regiones Promotoras Genéticas , ARN Bacteriano/análisis , ARN Mensajero/análisis , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Factor Rho/genética
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