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Suppression of fungal β-glucan-induced plant defence in soybean (Glycine max L.) by cyclic 1,3-1,6-β-glucans from the symbiont Bradyrhizobium japonicum
Authors:Axel Mithöfer  Arvind A Bhagwat  Markus Feger  Jürgen Ebel
Institution:(1) Botanisches Institut der Universität, Menzinger Strasse 67, D-80638 München, Germany;(2) Agricultural Research Service, BARC-W, USDA, 20705 Beltsville, MD, USA;(3) Department of Agronomy, University of Maryland, 20742 College Park, MD, USA
Abstract:The production of antimicrobial phytoalexins is one of the best-known inducible defence responses following microbial infection of plants or treatment with elicitors. In the legume soybean (Glycine max L.), 1,3-1,6-beta-glucans derived from the fungal pathogen Phytophthora sojae have been identified as potent elicitors of the synthesis of the phytoalexin, glyceollin. Recently it has been reported that during symbiotic interaction between soybean and the nitrogen-fixing bacterium Bradyrhizobium japonicum USDA 110 the bacteria synthesize cyclic 1,3-1,6-beta-glucans. Here we demonstrate that both the fungal and the bacterial beta-glucans are ligands of beta-glucan-binding sites which are putative receptors for the elicitor signal compounds in soybean roots. Whereas the fungal beta-glucans stimulate phytoalexin synthesis at low concentrations, the bacterial cyclic 1,3-1,6-beta-glucans appear to be inactive even at relatively high concentrations. Competition studies indicate that increasing concentrations of the bacterial 1,3-1,6-beta-glucans progressively inhibit stimulation of phytoalexin synthesis in a bioassay induced by the fungal 1,3-1,6-beta-glucans. Another type of cyclic beta-glucan, a 1,2-beta-glucan from Rhizobium meliloti, that does not nodulate on soybean, seems to be inactive as elicitor and as ligand of the beta-glucan-binding sites. These results may indicate a novel mechanism for a successful plant-symbiont interaction by suppressing the plant's defence response.Abbreviations HG-APEA 1-2-(4-aminophenyl)ethyl]amino-l-hexaglucosyl]deoxyglucitol - HG-AzPEA l-2-(4-azidophenyl)-ethyl]amino-l-hexaglucosyl]deoxyglucitol - IC50 concentration for half-maximal displacement We thank Ines Arlt for excellent technical assistance. This work was supported by the Deutsche Forschungsgemeinschaft (SFB 369), the Bundesministerium für Bildung, Wissenschaft, Forschung und Technologie, Fonds der Chemischen Industrie (J.E.), and USDA CSRS NRI Competitive Research grant 93373059233 (A.A.B.).
Keywords:Bradyrhizobium  Bacterial/fungal 1  3-1  6-beta-glucans" target="_blank">gif" alt="beta" align="MIDDLE" BORDER="0">-glucans  Elicitor  Glycine  Phytoalexins  beta-Glucanbinding sites" target="_blank">gif" alt="beta" align="MIDDLE" BORDER="0">-Glucanbinding sites
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