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Enhanced proteolysis leads to pre-mature cell death under the influence of elicitor like mycelial components from karnal bunt (tilletia indica) pathogen in wheat callus cultures.
Indian J Exp Biol ; 2005 Aug; 43(8): 746-50
Artículo en Inglés | IMSEAR | ID: sea-57455
ABSTRACT
Calli raised from mature embryos of susceptible wheat cultivar WH 542 were used in the present study as in vitro bioassay system to study the influence of disease determinant(s) of Karnal bunt (Tilletia indica), a semi-biotrophic fungal pathogen of wheat. Influence of elicitor and conditioned medium (CM) prepared from fungal cultures of T. indica was investigated on induction of programmed cell death (PCD). Induction of PCD was observed as hypersensitive response (HR) in terms of browning at localized regions of callus cultures and induction of proteolytic enzyme(s). Elicitor treated calli showed higher induction of protease activity than untreated and CM-treated cultures, which showed not much change in the activity. It was further substantiated by gel protease assay and activation of caspase-3 like protein(s) in callus cultures that clearly suggested the presence of signaling molecule(s) in the fungal elicitor preparation rather than in conditioned medium. This study further demonstrated that only elicitor preparation possesses such molecule(s), which might be cell wall bound components, rather than secretory in nature as CM was unable to induce PCD in wheat callus cultivars.
Asunto(s)
Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Asunto principal: Péptido Hidrolasas / Enfermedades de las Plantas / Proteínas de Plantas / Basidiomycota / Triticum / Apoptosis / Meristema / Micelio Idioma: Inglés Revista: Indian J Exp Biol Año: 2005 Tipo del documento: Artículo

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Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Asunto principal: Péptido Hidrolasas / Enfermedades de las Plantas / Proteínas de Plantas / Basidiomycota / Triticum / Apoptosis / Meristema / Micelio Idioma: Inglés Revista: Indian J Exp Biol Año: 2005 Tipo del documento: Artículo