Physiological basis of UV-C induced resistance to Botrytis cinerea in tomato fruit. V. Constitutive defence enzymes and inducible pathogenesis-related proteins
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作者:
Charles, Marie Therese
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Univ Laval, Dept Food Sci & Nutr, Quebec City, PQ G1V 0A6, Canada
Univ Laval, Hort Res Ctr, Quebec City, PQ G1V 0A6, CanadaUniv Laval, Dept Food Sci & Nutr, Quebec City, PQ G1V 0A6, Canada
Charles, Marie Therese
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Tano, Kablan
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Univ Laval, Dept Food Sci & Nutr, Quebec City, PQ G1V 0A6, Canada
Univ Laval, Hort Res Ctr, Quebec City, PQ G1V 0A6, CanadaUniv Laval, Dept Food Sci & Nutr, Quebec City, PQ G1V 0A6, Canada
Changes in the protein content and profile of postharvest tomato fruit treated with the hormetic dose (3.7 kJ m(-2)) of ultraviolet light C (UV-C) at the mature green stage was investigated. In UV-C treated fruits, the total protein content increased until 10 d after treatment and decreased thereafter during a 30 d storage period; whereas in control fruit, protein content decreased constantly throughout the storage period. Using polyacrylamide gel electrophoresis (PAGE) it was shown that UV-C treatment affected the protein profile of tomato fruit in several manners: (1) UV-C repressed the expression of some proteins presumably associated with ripening; (2) it enhanced the expression of several constitutive proteins, of which one was an acidic beta-1,3-glucanase, three acidic chitinases and three basic chitinases; and (3) it induced the synthesis of at least 5 new proteins of which four were basic proteins. Among the proteins induced by UV-C, three (a basic beta-1,3-glucanase and two acidic chitinases) were apparently pathogenesis-related proteins as they were also induced by inoculation with Beotrytis cinerea. The molecular mass (MM) of five of the UV-C induced proteins was determined using SDS-PAGE. Their molecular masses were 45, 39.4, 34.6. 10 and 8.9 kDa. The UV-C induced beta-1,3-glucanase had a MM of 33.1 kDa. The MM of two constitutive chitinases were 48.3 and 30.5 kDa, and those of the two UV-C and pathogenesis-induced chitinases were 37,1 and 20.6 kDa. Furthermore, the glucanohydrolase activities induced by UV-C were maintained until the end of the storage period. It is likely that the PR-proteins with glucanohydrolase activities induced by UV-C are an integral part of the long-term resistance observed in UV-C treated tomato fruit. (C) 2008 Elsevier B.V. All rights reserved.