Cerebrosides A and C, sphingolipid elicitors of hypersensitive cell death and phytoalexin accumulation in rice plants

被引:129
作者
Koga, J
Yamauchi, T
Shimura, M
Ogawa, N
Oshima, K
Umemura, K
Kikuchi, M
Ogasawara, N
机构
[1] Meiji Seika Kaisha Ltd, Biosci Labs, Sakado, Saitama 3500289, Japan
[2] Plant Biol Def Syst Labs, Niigata 9590422, Japan
[3] Denka Seiken Co Ltd, Div Res & Dev, Niigata 9591836, Japan
关键词
D O I
10.1074/jbc.273.48.31985
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
When plants interact with certain pathogens, they protect themselves by generating various chemical and physical barriers called the hypersensitive response. These barriers are induced by molecules called elicitors that are produced by pathogens. In the present study, the most active elicitors of the hypersensitive response in rice were isolated from the rice pathogenic fungus Magnaporthe grisea, and their structures were identified as cerebrosides A and C, sphingolipids that were previously isolated as inducers of cell differentiation in the fungus Schizophyllum commune. Treatment of rice leaves with cerebroside A induced the accumulation of antimicrobial compounds (phytoalexins), cell death, and increased resistance to subsequent infection by compatible pathogens. The degradation products of cerebroside A (fatty acid methyl ester, sphingold base, and glucosyl sphingoid base) showed no elicitor activity. Hydrogenation of the 8E-double bond in the sphingold base moiety or the 3E-double bond in the fatty acid moiety of cerebroside A did not alter the elicitor activity, whereas hydrogenation of the 4E-double bond in the sphingold base moiety led to a 12-fold decrease in elicitor activity. Furthermore, glucocerebrosides hom Gaucher's spleen consisting of (E)-4-sphingenine and cerebrosides hom rice bran mainly consisting of (4E,8E)-4,8-sphingadienine and (4E,8Z)-4,8-sphingadienine showed no elicitor activity. These results indicate that the methyl group at C-9 and the 4E-double bond in the sphingoid base moiety of cerebrosides A and C are the key elements determining the elicitor activity of these compounds. This study is the first to show that sphingolipids have elicitor activity in plants.
引用
收藏
页码:31985 / 31991
页数:7
相关论文
共 49 条
[1]  
BIELAWSKA A, 1993, J BIOL CHEM, V268, P26226
[2]   EICOSAPENTAENOIC AND ARACHIDONIC ACIDS FROM PHYTOPHTHORA-INFESTANS ELICIT FUNGITOXIC SESQUITERPENES IN THE POTATO [J].
BOSTOCK, RM ;
KUC, JA ;
LAINE, RA .
SCIENCE, 1981, 212 (4490) :67-69
[3]  
BREMER EG, 1984, J BIOL CHEM, V259, P6818
[4]   CHEMICAL ACTIVATION OF HOST DEFENCE MECHANISMS AS A BASIS FOR CROP PROTECTION [J].
CARTWRIGHT, D ;
LANGCAKE, P ;
PRYCE, RJ ;
LEWORTHY, DP ;
RIDE, JP .
NATURE, 1977, 267 (5611) :511-513
[5]  
Dangl JL, 1996, PLANT CELL, V8, P1793, DOI 10.1105/tpc.8.10.1793
[6]   Requirement for GD3 ganglioside in CD95- and ceramide-induced apoptosis [J].
DeMaria, R ;
Lenti, L ;
Malisan, F ;
dAgostino, F ;
Tomassini, B ;
Zeuner, A ;
Rippo, MR ;
Testi, R .
SCIENCE, 1997, 277 (5332) :1652-1655
[7]   ARABIDOPSIS MUTANTS SIMULATING DISEASE RESISTANCE RESPONSE [J].
DIETRICH, RA ;
DELANEY, TP ;
UKNES, SJ ;
WARD, ER ;
RYALS, JA ;
DANGL, JL .
CELL, 1994, 77 (04) :565-577
[8]  
Dixon R A, 1990, Adv Genet, V28, P165
[9]   MOLECULAR-SPECIES OF CERAMIDE AND MONO-GLYCOSYLCERAMIDE, DI-GLYCOSYLCERAMIDE, TRI-GLYCOSYLCERAMIDE, AND TETRAGLYCOSYLCERAMIDE IN BRAN AND ENDOSPERM OF RICE GRAINS [J].
FUJINO, Y ;
OHNISHI, M ;
ITO, S .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1985, 49 (09) :2753-2762
[10]   Programmed cell death: A way of life for plants [J].
Greenberg, JT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) :12094-12097