Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Más filtros











Base de datos
Intervalo de año de publicación
2.
J Fish Dis ; 32(8): 645-53, 2009 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-19500208

RESUMEN

A multiplex polymerase chain reaction protocol for the detection of Photobacterium damselae and subspecies piscicida and damselae discrimination, with internal amplification control, was developed. Assay specificity was assessed by testing 19 target and 25 non-target pure cultures. The detection limit was 500 fg, corresponding to 100 genome equivalents. The optimized protocol was also prevalidated with spleen, kidney and blood samples from infected and uninfected sea bass, without any culture step, and it can be proposed as a valid alternative to culture standard methods for the rapid and specific diagnosis of photobacteriosis in fish.


Asunto(s)
Lubina/microbiología , Photobacterium/genética , Reacción en Cadena de la Polimerasa/métodos , Animales , Secuencia de Bases , Datos de Secuencia Molecular , Oligonucleótidos/genética , Sensibilidad y Especificidad , Alineación de Secuencia , Análisis de Secuencia de ADN
3.
J Fish Dis ; 32(9): 745-53, 2009 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-19490395

RESUMEN

Abstract Cobalamin (vitamin B(12)) is an essential cofactor in a variety of enzymatic reactions and most prokaryotes contain transport systems to import vitamin B(12). A gene coding for a periplasmic cobalamin-binding protein of Photobacterium damselae subsp. piscicida was identified by in silico analysis of sequences from a genomic library. The open reading frame was composed of 834 bp encoding a protein of 277 amino acids. The protein showed 61% identity with the vitamin B(12)-binding protein precursor of P. profundum, 53% identity with the corresponding protein of Vibrio parahaemolyticus and 43% identity with the periplasmic binding protein BtuF of Escherichia coli. The expression of the native protein was investigated in P. damselae subsp. piscicida, but BtuF was weakly expressed under normal conditions. To characterize the BtuF of P. damselae subsp. piscicida, the recombinant protein was expressed with a C-terminal His(6)-tag and purified; the molecular weight was estimated to be approximately 30 kDa. The protein does not contain any free thiol group, consistent with the view that the two cysteine residues are involved in a disulphide bond. The purified BtuF binds cyanocobalamin with an affinity constant of 6 +/- 2 microm.


Asunto(s)
Regulación de la Expresión Génica , Proteínas Periplasmáticas/genética , Proteínas Periplasmáticas/metabolismo , Photobacterium/fisiología , Transcobalaminas/genética , Transcobalaminas/metabolismo , Secuencia de Aminoácidos , Datos de Secuencia Molecular , Proteínas Periplasmáticas/química , Filogenia , Unión Proteica , Proteínas Recombinantes/metabolismo , Alineación de Secuencia , Transcobalaminas/química , Vitamina B 12/metabolismo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA