บทคัดย่องานวิจัย

Characterization of extracellular lytic enzymes produced by the yeast biocontrol agent Candida oleophila

Meirav Bar-Shimon, Hila Yehuda, Lea Cohen, Batia Weiss, Alexsandra Kobeshnikov, Avinoam Daus, Martin Goldway, Michael Wisniewski and Samir Droby

Current Genetics 45 (3): 140-148. 2004.

2004

บทคัดย่อ

Characterization of extracellular lytic enzymes produced by the yeast biocontrol agent Candida oleophila The yeast Candida oleophila, the base of the commercial product Aspire, is recommended for the control of postharvest decay of citrus and pome fruit. Competition for nutrients and space is believed to be the major mode of action. Involvement of fungal cell wall-degrading enzymes is also suggested to play a role in the mechanism of action of yeast antagonists. The present study showed that the yeast C. oleophila is capable of producing and secreting various cell wall-degrading enzymes, including exo-b-1,3-glucanase, chitinase and protease. Exo-b-1,3-glucanase and chitinase were produced and maximized in the early stages of growth, whereas protease reached a maximum level o­nly after 6–8 days. Production of exo-b-1,3-glucanase, chitinase and protease was stimulated by the presence of cell wall fragments of Penicillium digitatumin the growth medium, in addition to glucose. This study also provided evidence that C. oleophila is capable of secreting exo-b-1,3-glucanase into the wounded surface of grapefruit. The role of exo-b-1,3-glucanase (CoEXG1) in the biocontrol activity of C. oleophila was tested using CoEXG1-knockouts and double-CoEXG1 over-producing transformants. In vitro bioassays showed that wild-type C. oleophila and exo-b-1,3-glucanase over-expressing transformants had similar inhibitory effects o­n spore germination and germ-tube elongation; and both were more inhibitory to the fungus than the knockout transformant. In experiments conducted o­n fruit to test the biocontrol activity against infection by P. digitatum, no significant difference in inhibition was observed between transformants and untransformed C. oleophila cells at the high concentrations of cells used, whereas at a lower concentration of yeast cells the knockout transformants appeared to be less effective.