Phytoalexins from Thlaspi arvense, a wild crucifer resistant to virulent Leptosphaeria maculans:: structures, syntheses and antifungal activity

被引:104
作者
Pedras, MSC [1 ]
Chumala, PB [1 ]
Suchy, M [1 ]
机构
[1] Univ Saskatchewan, Dept Chem, Saskatoon, SK S7N 5C9, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Thlaspi arvense; stinkweed; Brassicaceae; crucifer; G Leptosphaeria maculans; 4-methoxyindolyl-3-acetonitrile; Phoma lingam; phytoalexin; wasalexin A; wasalexin synthesis;
D O I
10.1016/S0031-9422(03)00441-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Phytoalexins are inducible chemical defenses produced by plants in response to diverse forms of stress, including microbial attack. Our search for phytoalexins from cruciferous plants resistant to economically important fungal diseases led us to examine stinkweed or pennycress (Thlaspi arvense), a potential source of disease resistance to blackleg. We have investigated phytoalexin production in leaves of T. arvense under abiotic (copper chloride) and biotic elicitation by Leptosphaeria maculans (Desm.) Ces. et de Not. [asexual stage Phoma lingam (Tode ex Fr.) Desm.], and report here two phytoalexins, wasalexin A and arvelexin (4-methoxyindolyl-3-acetonitrile), their syntheses and antifungal activity against isolates of P. lingam/L. maculans, as well as the isolation of isovitexin, a constitutive glycosyl flavonoid of stinkweed, having antioxidant properties but devoid of antifungal activity. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:949 / 956
页数:8
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