Physiological basis of UV-C induced resistance to Botrytis cinerea in tomato fruit. V. Constitutive defence enzymes and inducible pathogenesis-related proteins

被引:85
作者
Charles, Marie Therese [1 ,2 ]
Tano, Kablan [1 ,2 ]
Asselin, Alain [3 ]
Arul, Joseph [1 ,2 ]
机构
[1] Univ Laval, Dept Food Sci & Nutr, Quebec City, PQ G1V 0A6, Canada
[2] Univ Laval, Hort Res Ctr, Quebec City, PQ G1V 0A6, Canada
[3] Univ Laval, Dept Plant Sci, Quebec City, PQ G1V 0A6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Chitinase; Disease control; Gray mold; Glucanase; Host resistance; Hormetic; Hormic dose; Host defense mechanisms; Lycopersicon esculentum; Pathogenesis-related proteins (PR); Polyacrylamide gel electrophoresis; Postharvest pre-storage treatment; UV-light; BETA-1,3-GLUCANASE ACTIVITY; DIFFERENTIAL INDUCTION; PHYTOPHTHORA-INFESTANS; CLADOSPORIUM-FULVUM; ACQUIRED-RESISTANCE; INHIBITORY-ACTIVITY; ULTRAVIOLET-LIGHT; ACCUMULATION; ANTIFUNGAL; TOBACCO;
D O I
10.1016/j.postharvbio.2008.08.016
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
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.
引用
收藏
页码:414 / 424
页数:11
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