Muestra métricas de impacto externas asociadas a la publicación. Para mayor detalle:
| Indexado |
|
||||
| DOI | 10.1371/JOURNAL.PONE.0015979 | ||||
| Año | 2011 | ||||
| Tipo | artículo de investigación |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
This work shows that the recently described Escherichia coli BtuE peroxidase protects the bacterium against oxidative stress that is generated by tellurite and by other reactive oxygen species elicitors (ROS). Cells lacking btuE (Delta btuE) displayed higher sensitivity to K(2)TeO(3) and other oxidative stress-generating agents than did the isogenic, parental, wild-type strain. They also exhibited increased levels of cytoplasmic reactive oxygen species, oxidized proteins, thiobarbituric acid reactive substances, and lipoperoxides. E. coli Delta btuE that was exposed to tellurite or H(2)O(2) did not show growth changes relative to wild type cells either in aerobic or anaerobic conditions. Nevertheless, the elimination of btuE from cells deficient in catalases/peroxidases (Hpx(-)) resulted in impaired growth and resistance to these toxicants only in aerobic conditions, suggesting that BtuE is involved in the defense against oxidative damage. Genetic complementation of E. coli Delta btuE restored toxicant resistance to levels exhibited by the wild type strain. As expected, btuE overexpression resulted in decreased amounts of oxidative damage products as well as in lower transcriptional levels of the oxidative stress-induced genes ibpA, soxS and katG.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | ARENAS-SALINAS, FELIPE ALEJANDRO | Hombre |
Universidad de Santiago de Chile - Chile
|
| 2 | COVARRUBIAS-PIZARRO, PAULO CESAR | Hombre |
Universidad de Santiago de Chile - Chile
|
| 3 | SANDOVAL-CALQUIN, JUAN MARCELO | Hombre |
Universidad de Santiago de Chile - Chile
|
| 4 | Perez-Donosol, Jose Manuel | Hombre |
Universidad de Santiago de Chile - Chile
|
| 5 | Imlay, James A. | Hombre |
UNIV ILLINOIS - Estados Unidos
School of Molecular and Cellular Biology - Estados Unidos |
| 6 | VASQUEZ-EHRENFELD, CARLOS HUMBERTO | Hombre |
Universidad de Santiago de Chile - Chile
|
| Fuente |
|---|
| FONDECYT |
| CONICYT |
| Dicyt-USACH |
| National Institutes of Health |
| Universidad de Santiago de Chile |
| Dirección de Investigación |
| National Institute of General Medical Sciences |
| MECESUP, Chile |
| Agradecimiento |
|---|
| F.A.A. received doctoral fellowships from Conicyt and MECESUP UCH407, Chile. J.M.P. was sponsored by a postdoctoral fellowship from Direccion de Investigacion, Universidad de Santiago de Chile. J.M.S. received a doctoral fellowship from MECESUP, Chile. This work was supported by grants # 1090097 from Fondecyt and Dicyt-USACH, to C.C.V, and from National Institutes of Health grant GM049640 to J.A.I. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. |