Abstract

AbstractLeaves of eucalyptus (Eucalyptus urophylla) were infiltrated with a cell suspension of the incompatible pathogen Acidovorax avenae pv. avenae and showed a typical hypersensitive response within 24h. Necrotic leaf areas were excised, vacuum infiltrated with 40% ethanol and left under continuous agitation at room temperature for 24h. The diffusate was concentrated, partitioned with ethyl‐acetate, concentrated to dryness and resuspended in a small volume of methanol. The biological activity of extracts was evaluated by an agar diffusion method against noncompatible bacteria (A. avenae pv. avenae and Xanthomonas axonopodis pv. manihotis) and fungi (Penicillium sp. and Aspergillus sp.). Inhibition haloes, when present, were always larger in extracts from leaves infiltrated with the incompatible bacterium than the water control. Thin layer chromatography resolution of crude extracts from leaves infiltrated with both incompatible pathogen cell suspension and water, followed by bioautography with Thieleviopsis paradoxa, consistently rendered, in both situations, a large, diffuse inhibition halo near the origin, assumed to be due to preformed antimicrobial substances. However, extracts from leaves infiltrated with the living cells of the incompatible pathogen gave rise to a smaller, second inhibition halo, near the front, that was interpreted as being one or several phytoalexins.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call