Degradation of Cercosporin by laccase
a technology of laccase and cercosporin, which is applied in the direction of biocide, animal husbandry, peptide/protein ingredients, etc., can solve the problems of severe blighting of leaf tissue, cell death, and rupture of plant plasma membranes, and achieve the effect of preventing or minimizing damage to plants
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Microorganisms and Culture Conditions
[0115]Cercospora beticola Sacc. isolate C2 (Whitney et al., 1976, Phytopathology, 66:1158-1160) was provided by John J. Weiland, USDA, Fargo, N.Dak. and isolate S2 was isolated from sugar beet fields at Sidney, Mont., and was provided by Anthony J. Caesar, USDA, Sidney, Mont. Both isolates of C. beticola were cultured on potato dextrose agar (PDA, DIFCO Laboratories), at 23° C. with a 5 hr photoperiod (light source was fluorescent light with an intensity of 45 μmol m−2s−1) for maximum production of cercosporin. Three week-old cultures were used for extraction of cercosporin.
Cercosporin Extraction
[0116] Cercosporin is visible as a red pigment on the underside of cultures growing on agar medium. Cercosporin was extracted following a modified procedure of Daub (1982, ibid). Briefly, the agar containing the fungal mycelia was removed and placed on plastic screens in a laminar flow hood to allow them to dry for 2-3 days. Dried...
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