Abstract
Plants respond to invasive microorganisms in a variety of ways (Bell 1981). Among these, the synthesis and accumulation of toxic molecules called phytoalexins is a response observed in a number of plant-pathogen interactions (Dixon 1986; Ebel 1986). Phytoalexins accumulate rapidly at the site of infection, and reach levels inhibitory to microbial growth quickly enough to play a role in defense against disease (Hahn et al 1985). Several studies have demonstrated that phytoalexin accumulation is limited, in incompatible (plant resistant) responses, to the immediate vicinity of the infection (Mansfield et al 1974; Moesta et al 1982; Mayama & Tani. 1982; Hahn et al 1985). These observations are important since phytoalexins are toxic to both plaqt and microbial cells (Smith 1982; Weinstein & Albersheim 1983).
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References
Bell AA (1981) Biochemical mechanisms of disease resistance. Ann Rev Plant Physiol 32:21–81
Birberg W, Fügedi P, Garegg PJ, Pilotti Ä (1989) Syntheses of a heptasaccharide β-linked to an 8- methoxycarbonyl-oct-l-yl linking arm and of a decasaccharide with structures corresponding to the phytoelicitor active glucan of Phytophthora megasperma f.sp. glycinea. J Carbohydr Chem 8:47–57
Bruce RJ, West CA (1982) Elicitation of casbene synthetase activity in castor bean. The role of pectic fragments of the plant cell wall in elicitation by a fungal endopolygalacturonase. Plant Physiol 69:1181–1188
Cervone F, De Lorenzo G, Degrä L, Salvi G (1987) Elicitation of necrosis in Vigna unguiculata Walp. by homogeneous Aspergillus niger endo-polygalacturonase and by a-d-galacturonate oligomers. Plant Physiol 85:626–630
Chaves das Neves HJ, Riscado AMV, Frank H (1986) Derivatives for the analysis of monosaccharides by capillary G.L.C.: Trimethylsilylated deoxy(methoxyamino)alditols. Carbohydr Res 152:1–6
Darvill AG, Albersheim P (1984) Phytoalexins and their elicitors — A defense against microbial infection in plants. Ann Rev Plant Physiol 35:243–275
Davis KR, Lyon GD, Darvill AG, Albersheim P (1984) Host-pathogen interactions. XXV. Endopolygalacturonic acid lyase from Erwinia carotovora elicits phytoalexin accumulation by releasing plant cell wall fragments. Plant Physiol 14:52–60
Davis KR, Darvill AG, Albersheim P (1986a) Host-pathogen interactions. XXXI. Several biotic and abiotic elicitors act synergistically in the induction of phytoalexin accumulation in soybean. Plant Mol Biol 6:23–32
Davis KR, Darvill AG, Albersheim P, Dell A (1986b) Host-pathogen interactions. XXX. Characterization of elicitors of phytoalexin accumulation in soybean released from soybean cell walls by endopolygalacturonic acid lyase. Z Naturforsch 41c:39–48
Davis KR, Hahlbrock K (1987) Induction of defense responses in cultured parsley cells by plant cell wall fragments. Plant Physiol 85:1286–1290
Dixon RA (1986) The phytoalexin response: elicitation, signalling and control of host gene expression. Biol Rev 61:239–291
Ebel J (1986) Phytoalexin synthesis: The biochemical analysis of the induction process. Ann Rev Phytopathol 24:235–264
Farmer EE, Helgeson JP (1987) An extracellular protein from Phytophthora paprsitica var. nicotianae is associated with stress metabolite accumulation in tobacco callus. Plant Physiol 85:733–740
Fügedi P, Birberg W, Garegg PJ, Pilotti Å (1987) Syntheses of a branched heptasaccharide having phytoalexin-elicitor activity. Carbohydr Res 164:297–312
Fügedi P, Garegg PJ, Kvarnström I, Svansson L (1988) Synthesis of a heptasaccharide, structurally related to the phytoelicitor active glucan of Phytophthora megasperma f. sp. glycinea. J Carbohydr Chem 7:389–397
Hahn MG, Darvill AG, Albersheim P (1981) Host-pathogen interactions. XIX. The endogenous elicitor, a fragment of a plant cell wall polysaccharide that elicits phytoalexin accumulation in soybeans. Plant Physiol 68:1161–1169
Hahn MG, Bonhoff A, Grisebach H (1985) Quantitative localization of the phytoalexin glyceollin I in relation to fungal hyphae in soybean roots infected with Phytophthora megasperma f. sp. glycinea. Plant Physiol 77:591–601
Hahn MG, Bucheli P, Cervone F, Doares SH, O’Neill RA, Darvill A, Albersheim P (1989) The roles of cell wall constituents in plant-pathogen interactions. In: Nester E, Kosuge T (eds) Plant-Microbe Interactions, Volume 3. McGraw Hill, New York, in press
Jin DF, West CA (1984) Characteristics of galacturonic acid oligomers as elicitors of casbene synthetase activity in castor bean seedlings. Plant Physiol 74:989–992
Keen NT (1975) Specific elicitors of plant phytoalexin production: Determinants of race specificity in pathogens? Science 187:74–75
Mansfield JW, Hargreaves JA, Boyles FC (1974) Phytoalexin production by live cells in broad bean leaves infected with Botrytis cinerea. Nature 252:316–317
Mayama S, Tani T (1982) Microspectrophotometric analysis of the location of avenalumin accumulation in oat leaves in response to fungal infection. Physiol Plant Pathol 21:141–149
Mester L, El Khadem HS (1980) Hydrazine derivatives and related compounds. In: Pigman W, Horton D, Wander JD (eds) The Carbohydrates, Vol. IB, Chemistry and Biochemistry. Academic Press, New York, p 929–988
Moesta P, Seydel U, Lindner B, Grisebach H (1982) Detection of glyceollin on the cellular level in infected soybean by laser microprobe mass analysis. ZNaturforsch 37c:748–751
Nakahara Y, Ogawa T (1987) Synthetic studies on plant cell-wall glycans. 3. Stereocontrolled, total synthesis of α-D-GalA-[(l-→4)-α-d-GalA]8-(l-→4)-β-d-GalA-l-→OPr, a synthetic model for phytoalexin elictor- active oligogalacturonic acids. CarbohydrRes 167:cl-c7
Nakahara Y, Ogawa T (1989) Total synthesis of galactododecaosiduronic acid, an endogenous phytoalexin elicitor isolated from soybean cell wall. Tetrahedr Lett 30:87–90
Nothnagel EA, McNeil M, Albersheim P, Dell A (1983) Host-pathogen interactions. XXII. A galacturonic acid oligosaccharide from plant cell walls elicits phytoalexins. Plant Physiol 71:916–926
Ossowski P, Pilotti Å, Garegg PJ, Lindberg B (1984) Synthesis of a glucoheptaose and a glucooctaose that elicit phytoalexin accumulation in soybean. J Biol Chem 259:1137–1140
Sharp JK, Albersheim P, Ossowski P, Pilotti Å, Garegg PJ, Lindberg B (1984a) Comparison of the structures and elicitor activities of a synthetic and a mycelial-wall-derived hexa(β-d-glucopyranosyl)-d- glucitol. J Biol Chem 259:11341–11345
Sharp JK, McNeil M, Albersheim P (1984b) The primary structures of one elicitor-active and seven elicitorinactive hexa(β-d-glucopyranosyl)-d-glucitols isolated from the mycelial walls of Phytophthora megasperma f. sp. glycinea. J Biol Chem 259:11321–11336
Sharp JK, Valent B, Albersheim P (1984c) Purification and partial characterisation of a β-glucan fragment that elicits phytoalexin accumulation in soybean. J Biol Chem 259:11312–11320
Smith DA (1982) Toxicity of phytoalexins. In: Bailey JA, Mansfield JW (eds) Phytoalexins. Blackie, Glasgow and London, p 218–252
Walker-Simmons M, Hadwiger L, Ryan CA (1983) Chitosans and pectic polysaccharides both induce the accumulation of the antifungal phytoalexin pisatin in pea pods and antinutrient proteinase inhibitors in tomato leaves. Biochem Biophys Res Commun 110:194–199
Wang WT, LeDonne NC Jr, Ackerman B, Sweeley CC (1984) Structural characterisation of oligosaccharides by high-performance liquid chromatography, fast-atom bombardment-mass spectrometry, and exoglygosidase digestion. Anal Biochem 141:366–381
Weinstein LA, Albersheim P (1983) Host-pathogen interactions. XXIII. The mechanism of the antibacterial action of glycinol, a pterocarpan phytoalexin synthesized by soybeans. Plant Physiol 72:557–563
West CA (1981) Fungal elicitors of the phytoalexin response in higher plants. Naturwissenschaften 68:447–457
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© 1989 Springer-Verlag Berlin Heidelberg
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Hahn, M.G. et al. (1989). Elicitation of Phytoalexins by Synthetic Oligoglucosides, Synthetic Oligogalacturonides, and their Derivatives. In: Lugtenberg, B.J.J. (eds) Signal Molecules in Plants and Plant-Microbe Interactions. NATO ASI Series, vol 36. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-74158-6_9
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DOI: https://doi.org/10.1007/978-3-642-74158-6_9
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