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Proteomics ; 9(8): 2273-85, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19382143

RESUMEN

In this study, the stable consortium composed by Pseudomonas reinekei strain MT1 and Achromobacter xylosoxidans strain MT3 (cell numbers in proportion 9:1) was under investigation to reveal bacterial interactions that take place under severe nutrient-limiting conditions. The analysis of steady states in continuous cultures was carried out at the proteome, metabolic profile, and population dynamic levels. Carbon-limiting studies showed a higher metabolic versatility in the community through upregulation of parallel catabolic enzymes (salicylate 5-hydroxylase and 17-fold on 2-keto-4-pentenoate hydratase) indicating a possible alternative carbon routing in the upper degradation pathway highlighting the effect of minor proportions of strain MT3 over the major consortia component strain MT1 with a significant change in the expression levels of the enzymes of the mainly induced biodegradation pathway such as salicylate 1-hydroxylase and catechol 1,2-dioxygenase together with important changes in the outer membrane composition of P. reinekei MT1 under different culture conditions. The study has demonstrated the importance of the outer membrane as a sensing/response protective barrier caused by interspecies interactions highlighting the role of the major outer membrane proteins OprF and porin D in P. reinekei sp. MT1 under the culture conditions tested.


Asunto(s)
Achromobacter denitrificans/metabolismo , Proteoma/biosíntesis , Pseudomonas/metabolismo , Salicilatos/metabolismo , Achromobacter denitrificans/química , Proteínas de la Membrana Bacteriana Externa/biosíntesis , Proteínas Bacterianas/biosíntesis , Proteínas Bacterianas/química , Catecol 1,2-Dioxigenasa/biosíntesis , Hidrolasas/biosíntesis , Cetoácido Reductoisomerasa/biosíntesis , Redes y Vías Metabólicas , Metaboloma , Oxigenasas de Función Mixta/biosíntesis , Estrés Oxidativo , Factores de Elongación de Péptidos/biosíntesis , Proteoma/química , Pseudomonas/química , Especificidad de la Especie , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción
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