Histology of disease development in resistant and susceptible cultivars of chickpea (Cicer arietinum L.) inoculated with spores of Ascochyta rabiei. Regulation of Phytoalexin Synthesis in Jackbean Callus Cultures. Plant Cell Tissue Organ Cult., 99 (1), 35-45. Acquisition of callogenic capacity in date palm leaf tissues in response to 2, 4-D treatment. La culture des tissus végétaux: techniques et réalisations. Management options for minimizing the damage by Ascochyta blight (Ascochyta rabiei) in chickpea (Cicer arietinum L.). Response to chitin in suspension-cultured Citrus aurantium cells.
Hormonal Control of Cell Proliferation and Xylem Differentiation in Cultured Tissues of Glycine max var. In planta identification of putative pathogenicity factors from the chickpea pathogen Ascochyta rabiei by de novo transcriptome sequencing using RNA-Seq and massive analysis of cDNA ends. FAO, Food and agriculture United Nations Organization (2015).Suppression of the hypersensitive response of potato tuber protoplasts to hyphal wall components by water soluble glucans isolated from Phytophthora infestans. Infection of Tobacco callus by Phytophthora paraitca var. Involvement of phenolic compounds in the resistance of grapevine callus to downy mildew (Plasmopara viticola). Les composés phénoliques et la résistance des plantes aux agents pathogènes. Biochemistry and molecular biology of plants 2nd edition, John Wiley and Sons.
Characterization of secondary metabolites in culture media and host responses to the pathogens in calli. Effects of three esca-associated fungi on Vitis vinifera L.: I. Plant biotechnology and agriculture: prospects for the 21st century.
Keywords: Cicer arietinum, Pathosystem, In vitro culture, Chickpea blight In INRA199, the pathogen proliferation was slow and limited by the formation of an area where the cells accumulated phenolic compounds whereas in the cultivar Zouaoui the pathogen rapidly colonized the calli intercellular space and the number of formed pycnidia was high. The histological study of calli inoculated with Ascocchyta rabiei spore suspension compared to the control showed two different reactions. Murashige and Skoog, (1962) medium supplemented with 0.5 mg/l of Naphthalene Acetic Acid (NAA) and 1 mg/l of Benzyl Amino Purine (BAP) were used for the production of calluses used as a host. A resistant chickpea genotype INRA 199 and a local cultivar “Zouaoui ” were used. The objective of this research was to study the interaction between Ascochyta rabiei as a pathogen and its host, established through in vitro tissue culture using as a pathosystem chickpea Cicer arietinum callus inoculated with Ascochyta rabiei spores.
0 kommentar(er)
