Effects of chrysophanol, parietin, and nepodin of Rumex crispus on barley and cucumber powdery mildews

被引:84
作者
Choi, GJ [1 ]
Lee, SW [1 ]
Jang, KS [1 ]
Kim, JS [1 ]
Cho, KY [1 ]
Kim, JC [1 ]
机构
[1] Korea Res Inst Chem Technol, Biol Funct Res Team, Taejon 305600, South Korea
关键词
chrysophanol; parietin; nepodin; powdery mildew; Rumex crispus;
D O I
10.1016/j.cropro.2004.05.005
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 [作物学];
摘要
Three substances that show antifungal activity against Blumeria graminis f. sp. hordei were isolated from roots of Rumex crispus and identified as chrysophanol, parietin, and nepodin. The substances were tested for plant disease control activity in vivo against six plant pathogenic fungi. All specifically reduced the development of barley powdery mildew. The concentrations required for 50% disease control were 4.7 mug/ml for chrysophanol, 0.48 mug/ml for parietin, and 20 mug/ml for nepodin. These agents showed both curative and protective activity against barley powdery mildew. Chrysophanol (100 mug/ml) and nepodin (400 mug/ml) were more effective than the fungicides fenarimol (30 mug/ml) and polyoxin B (100 mug/ml), under glasshouse conditions, against cucumber powdery mildew, which is caused by Podosphaera xanthii. Parietin (30 and 10 mug/ml) reduced the development of cucumber powdery mildew as efficiently as fenarimol (30 mug/ml) and more effectively than polyoxin B (100 mug/ml). (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1215 / 1221
页数:7
相关论文
共 35 条
[1]
Second and higher order boundary value problems of nonsingular type [J].
Agarwal, RP ;
O'Regan, D .
BULLETIN OF THE BELGIAN MATHEMATICAL SOCIETY-SIMON STEVIN, 2000, 7 (01) :43-52
[2]
Ayyangar N.R., 1961, J SCI IND RES, V20B, P493
[3]
TOXICITY AND MUTAGENICITY OF MOLDS OF THE ASPERGILLUS-GLAUCUS GROUP - IDENTIFICATION OF PHYSCION AND 3 RELATED ANTHRAQUINONES AS MAIN TOXIC CONSTITUENTS FROM ASPERGILLUS-CHEVALIERI [J].
BACHMANN, M ;
LUTHY, J ;
SCHLATTER, C .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1979, 27 (06) :1342-1347
[4]
Bélanger RR, 2002, POWDERY MILDEWS: A COMPREHENSIVE TREATISE, P256
[5]
Antiplasmodial and antioxidant isofuranonaphthoquinones from the roots of Bulbine capitata [J].
Bezabih, M ;
Abegaz, BM ;
Dufall, K ;
Croft, K ;
Skinner-Adams, T ;
Davis, TME .
PLANTA MEDICA, 2001, 67 (04) :340-344
[6]
CADAVID I, 1985, International Journal of Crude Drug Research, V23, P13
[7]
In vitro antimutagenic effects of anthraquinone aglycones and naphthopyrone glycosides from Cassia tora [J].
Choi, JS ;
Lee, HJ ;
Park, KY ;
Ha, JO ;
Kang, SS .
PLANTA MEDICA, 1997, 63 (01) :11-14
[8]
Comparative evaluation of antioxidant potential of alaternin (2-hydroxyemodin) and emodin [J].
Choi, JS ;
Chung, HY ;
Jung, HA ;
Park, HJ ;
Yokozawa, T .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2000, 48 (12) :6347-6351
[9]
Copping LG, 2000, PEST MANAG SCI, V56, P651, DOI 10.1002/1526-4998(200008)56:8<651::AID-PS201>3.0.CO
[10]
2-U