Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros

Bases de datos
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
Arch Microbiol ; 197(1): 79-89, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-25362506

RESUMEN

Nitrosomonas europaea and Nitrobacter winogradskyi were grown singly and in co-culture in chemostats to probe for physiological differences between the two growth conditions. Co-culture growth medium containing 60 mM NH4 (+) resulted in a cell density (0.20-0.29 OD600) greater than the sum of the densities in single chemostat cultures, i.e., 0.09-0.14 OD600 for N. europaea with 60 mM NH4 (+)and 0.04-0.06 OD600 for N. winogradskyi with 60 mM NO2 (-). The NO2 (-)- and NH4 (+)-dependent O2 uptake rates, qRT-PCR, and microscopic observations indicated that in co-culture, N. europaea contributed ~0.20 OD600 (~80 %) and N. winogradskyi ~0.05 OD600 (~20 %). In co-culture, the transcriptomes showed that the mRNA levels of 773 genes in N. europaea (30.2 % of the genes) and of 372 genes in N. winogradskyi (11.8 % of the genes) changed significantly. Total cell growth and the analysis of the transcriptome revealed that in co-culture, N. europaea benefits more than N. winogradskyi.


Asunto(s)
Interacciones Microbianas , Nitrobacter/crecimiento & desarrollo , Nitrobacter/metabolismo , Nitrosomonas europaea/crecimiento & desarrollo , Nitrosomonas europaea/metabolismo , Amoníaco/metabolismo , Carga Bacteriana , Dióxido de Carbono/metabolismo , Técnicas de Cocultivo , Medios de Cultivo , Metabolismo Energético , Expresión Génica , Genes Bacterianos , Movimiento , Nitritos/metabolismo , Nitrobacter/genética , Nitrosomonas europaea/genética , Consumo de Oxígeno , Transcripción Genética , Transcriptoma
2.
Mol Plant Microbe Interact ; 18(4): 275-82, 2005 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-15828679

RESUMEN

Pathovars of Pseudomonas syringae interact with their plant hosts via the action of Hrp outer protein (Hop) effector proteins, injected into plant cells by the type III secretion system (TTSS). Recent availability of complete genome sequences for a number of P. syringae pathovars has led to a significant increase in the rate of effector discovery. However, lack of a systematic nomenclature has resulted in multiple names being assigned to the same Hop, unrelated Hops designated by the same alphabetic character, and failure of name choices to reflect consistent standards of experimental confirmation or phylogenetic relatedness. Therefore, specific experimental and bioinformatic criteria are proposed for proteins to be designated as Hops. A generic Hop name structure, HopXY#pv strain, also is proposed, wherein family membership is indicated by the alphabetic characters, subgroup membership numerically, and source pathovar and strain in subscript. Guidelines are provided for phylogenetic characterization and name selection for Hops that are novel, related to previously characterized Hops, chimeras, pseudogenes, truncations, or nonexpressed alleles. Phylogenetic analyses of previously characterized Hops are described, the results of which have been used to guide their integration into the proposed nomenclature.


Asunto(s)
Proteínas Bacterianas/genética , Pseudomonas syringae/genética , Terminología como Asunto , Proteínas Bacterianas/clasificación , Guías como Asunto , Funciones de Verosimilitud , Filogenia
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA