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| DOI | 10.1016/J.IJHYDENE.2012.11.007 | ||||
| Año | 2013 | ||||
| Tipo | artículo de investigación |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
Ethanoligenens harbinense is a promising hydrogen producing microorganism due to its high inherent hydrogen production rate. Even though the effect of media optimization and inhibitory metabolites has been studied in order to improve the hydrogen productivity of these cultures, the identification of the underlying causes of the observed changes in productivity has not been targeted to date. In this work we present a genome based metabolic flux analysis (MFA) framework, for the comprehensive study of E. harbinense in culture, and the effect of inhibitory metabolites and media composition on its metabolic state. A metabolic model was constructed for E. harbinense based on its annotated genome sequence and proteomic evidence. This model was employed to perform MFA and obtain the intracellular flux distribution under different culture conditions. These results allow us to identify key elements in the metabolism that can be associated to the observed production phenotypes, and that can be potential targets for metabolic engineering in order to enhanced hydrogen production in E. harbinense. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | CASTRO-FIGUEROA, JEAN FRANCO | Hombre |
Universidad de Chile - Chile
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| 2 | RAZMILIC-NEIRA, VALERIA ISABEL | Mujer |
Universidad de Chile - Chile
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| 3 | GERDTZEN-HAKIM, ZIOMARA PATRICIA | - |
Universidad de Chile - Chile
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| Fuente |
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| CONICYT, Chile |
| Fondo Nacional de Desarrollo Científico y Tecnológico |
| Comisión Nacional de Investigación Científica y Tecnológica |
| Fondecyt, Chile |
| Comisión Nacional de Investigación CientÃfica y Tecnológica |
| Fondo Nacional de Desarrollo CientÃfico y Tecnológico |
| Agradecimiento |
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| J.F.C. and V.R. were supported by National Doctoral Scholarship, Conicyt, Chile. We acknowledge funding from Initiation Grant 11090268 from Fondecyt, Chile. |
| J.F.C. and V.R. were supported by National Doctoral Scholarship, Conicyt, Chile. We acknowledge funding from Initiation Grant 11090268 from Fondecyt, Chile . |