חיפוש מתקדם
Phytopathology
Guetsky, R., Department of Postharvest Science of Fresh Produce, Institute for Technology and Storage of Agricultural Products, Volcani Center, Bet Dagan 50250, Israel
Kobiler, I., Department of Postharvest Science of Fresh Produce, Institute for Technology and Storage of Agricultural Products, Volcani Center, Bet Dagan 50250, Israel
Wang, X., Donald Danforth Plant Science Center, 975 N. Warson Rd., St. Louis, MO 63132, United States
Perlman, N., Department of Postharvest Science of Fresh Produce, Institute for Technology and Storage of Agricultural Products, Volcani Center, Bet Dagan 50250, Israel
Gollop, N., Department of Postharvest Science of Fresh Produce, Institute for Technology and Storage of Agricultural Products, Volcani Center, Bet Dagan 50250, Israel
Avila-Quezada, G., Centro de Investigacion en Alimentación Y Desarrollo A.C. Unidad Delicias, Chihuahua, Mexico C.P. 33089, Mexico
Hadar, I., Department of Plant Pathology and Microbiology, Faculty of Agriculture, Hebrew University of Jerusalem, Rehovot 74100, Israel
Prusky, D., Department of Postharvest Science of Fresh Produce, Institute for Technology and Storage of Agricultural Products, Volcani Center, Bet Dagan 50250, Israel
During avocado fruit ripening, decreasing levels of the flavonoid epicatechin have been reported to modulate the metabolism of preformed antifungal compounds and the activation of quiescent Colletotrichum gloeosporioides infections. Epicatechin levels decreased as well when C. gloeosporioides was grown in the presence of epicatechin in culture. Extracts of laccase enzyme obtained from decayed tissue and culture media fully metabolized the epicatechin substrate within 4 and 20 h, respectively. Purified laccase protein from C. gloeosporioides showed an apparent MW of 60,000, an isoelectric point at pH 3.9, and maximal epicatechin degradation at pH 5.6. Inhibitors of fungal laccase such as EDTA and thioglycolic acid reduced C. gloeosporioides symptom development when applied to ripening susceptible fruits. Isolates of C. gloeosporioides with reduced laccase activity and no capability to metabolize epicatechin showed reduced pathogenicity on ripening fruits. On the contrary, Mexican isolates with increasing capabilities to metabolize epicatechin showed early symptoms of disease in unripe fruits. Transcript levels of cglac1, encoding C. gloeosporioides laccase, were enhanced during fungal development in the presence of epicatechin at pH 6.0, where avocado fruits are susceptible to fungal attack. But transcript increase was not detected at pH 5.0, where the fruit is resistant to fungal attack. The present results suggest that biotransformation of epicatechin by C. gloeosporioides in ripening fruits is followed by the decline of the preformed antifungal diene compound, resulting in the activation of quiescent infections. © 2005 The American Phytopathological Society.
פותח על ידי קלירמאש פתרונות בע"מ -
הספר "אוצר וולקני"
אודות
תנאי שימוש
Metabolism of the flavonoid epicatechin by laccase of Colletotrichum gloeosporioides and its effect on pathogenicity on avocado fruits
95
Guetsky, R., Department of Postharvest Science of Fresh Produce, Institute for Technology and Storage of Agricultural Products, Volcani Center, Bet Dagan 50250, Israel
Kobiler, I., Department of Postharvest Science of Fresh Produce, Institute for Technology and Storage of Agricultural Products, Volcani Center, Bet Dagan 50250, Israel
Wang, X., Donald Danforth Plant Science Center, 975 N. Warson Rd., St. Louis, MO 63132, United States
Perlman, N., Department of Postharvest Science of Fresh Produce, Institute for Technology and Storage of Agricultural Products, Volcani Center, Bet Dagan 50250, Israel
Gollop, N., Department of Postharvest Science of Fresh Produce, Institute for Technology and Storage of Agricultural Products, Volcani Center, Bet Dagan 50250, Israel
Avila-Quezada, G., Centro de Investigacion en Alimentación Y Desarrollo A.C. Unidad Delicias, Chihuahua, Mexico C.P. 33089, Mexico
Hadar, I., Department of Plant Pathology and Microbiology, Faculty of Agriculture, Hebrew University of Jerusalem, Rehovot 74100, Israel
Prusky, D., Department of Postharvest Science of Fresh Produce, Institute for Technology and Storage of Agricultural Products, Volcani Center, Bet Dagan 50250, Israel
Metabolism of the flavonoid epicatechin by laccase of Colletotrichum gloeosporioides and its effect on pathogenicity on avocado fruits
During avocado fruit ripening, decreasing levels of the flavonoid epicatechin have been reported to modulate the metabolism of preformed antifungal compounds and the activation of quiescent Colletotrichum gloeosporioides infections. Epicatechin levels decreased as well when C. gloeosporioides was grown in the presence of epicatechin in culture. Extracts of laccase enzyme obtained from decayed tissue and culture media fully metabolized the epicatechin substrate within 4 and 20 h, respectively. Purified laccase protein from C. gloeosporioides showed an apparent MW of 60,000, an isoelectric point at pH 3.9, and maximal epicatechin degradation at pH 5.6. Inhibitors of fungal laccase such as EDTA and thioglycolic acid reduced C. gloeosporioides symptom development when applied to ripening susceptible fruits. Isolates of C. gloeosporioides with reduced laccase activity and no capability to metabolize epicatechin showed reduced pathogenicity on ripening fruits. On the contrary, Mexican isolates with increasing capabilities to metabolize epicatechin showed early symptoms of disease in unripe fruits. Transcript levels of cglac1, encoding C. gloeosporioides laccase, were enhanced during fungal development in the presence of epicatechin at pH 6.0, where avocado fruits are susceptible to fungal attack. But transcript increase was not detected at pH 5.0, where the fruit is resistant to fungal attack. The present results suggest that biotransformation of epicatechin by C. gloeosporioides in ripening fruits is followed by the decline of the preformed antifungal diene compound, resulting in the activation of quiescent infections. © 2005 The American Phytopathological Society.
Scientific Publication
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