Cell Separation in Plants pp 165-178 | Cite as
Host Cell Wall Loosening and Separation by Plant Pathogens
Chapter
Abstract
To achieve infection, many microbial pathogens respond to numerous signals, physical and chemical, from their host plants. Some of these have been identified and are known to activate genes controlling infection; such as certain plant phenolics and expression of virulence genes of Agrobacterium tumefaciens and nodulation genes of Rhizobiwn spp., serinol on leaf surfaces of sugar cane which stimulates HS-toxin production by Helminthosporium sacchari, and α-tocopherol which results in formation of parasitic mycelium of Ustilago violacea (Halverson and Stacey, 1986).
Keywords
Plant Cell Wall Sclerotinia Sclerotiorum Abscission Zone Pectate Lyase Pectin Lyase
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References
- Baker CJ, Whalen CH, Korman RZ and Bateman DF (1979) α-L-Arabino-furanosidase from Sclerotinia sclerotiorum: purification, characterization and effects on plant cell walls and tissue. Phytopathology 69: 789–793CrossRefGoogle Scholar
- Bateman DF and Basham HG (1976) Degradation of plant cell walls and membranes by microbial enzymes. In: Heitefuss R and Williams PH (eds) Encyclopedia of Plant Physiology, vol. IV. Springer-Verlag, New York pp 316–355Google Scholar
- Bateman DF and Beer SV (1965) Simultaneous production and synergistic action of oxalic acid and polygalacturonase during pathogenesis by Sclerotium rolfsii. Phytopathology 55: 204–211PubMedGoogle Scholar
- Bauer WD, Bateman DF and Whalen CH (1977) Purification of an endo-β-1,4-galactanase produced by Sclerotinia sclerotiorumi effects on isolated plant cell walls and potato tissue. Phytopathology 67: 862–868CrossRefGoogle Scholar
- Ben Arie R, Kislev N and Frenkel C (1979) Ultrastructural changes in the cell walls of ripening apple and pear fruit. Plant Physiol 64: 197–202PubMedCrossRefGoogle Scholar
- Bishop CD and Cooper RM (1983) An ultrastructural study of vascular colonization in three vascular diseases. I. Colonization of susceptible varieties. Physiol Plant Pathol 23: 323–343CrossRefGoogle Scholar
- Boccara M, Diolez A, Rouve M and Kotoujansky A (1988) The role of individual pec tate lyases of Erwinia chrysanthemi strain 3937 in pathogenicity on Saintpaulia plants. Physiol Molec Plant Pathol 33: 95–104CrossRefGoogle Scholar
- Bratt RP, Brown AE and Mercer PC (1988) A role for hydrogen peroxide in degradation of flax fibres by Botrytis cinerea. Trans Br Mycol Soc 91: 481–488CrossRefGoogle Scholar
- Collmer A, Berman P and Mount MS (1982) Pectate lyase regulation and bacterial soft-rot pathogenesis. In Mount MS and Lacey GH (eds) Phytopathogenic Prokaryotes, Vol I. Academic Press, London, pp 395–422Google Scholar
- Collmer A and Keen NT (1986) Role of pectic enzymes in plant pathogenesis. Ann Rev Phytopath 24: 383–409CrossRefGoogle Scholar
- Cooper RM (1981) Pathogen-induced changes in host ultrastructure. In: Staples RC and Toenniesen GH (eds) Plant disease control: resistance and susceptibility. Wiley, New York, pp 105–142Google Scholar
- Cooper RM (1983) The mechanisms and significance of enzymic degradation of host cell walls by parasites. In: Callow J (ed) Biochemical Plant Pathology. John Wiley & Sons, New York, pp 101–135Google Scholar
- Cooper RM (1984) The role of cell wall-degrading enzymes in infection and damage. In Wood RKS and Jellis GJ (eds) Plant diseases: infection damage and loss. Blackwell Scientific Publications, Oxford, pp 13–28Google Scholar
- Cooper RM (1987) The use of mutants in exploring depolymerases as determinants of pathogenicity. In: Day PR and Jellis GJ (eds) Genetics and Plant Pathogenesis. Blackwell Scientific Publications, Oxford pp 261–281Google Scholar
- Cooper RM, Rankin B and Wood RKS (1978) Cell wall-degrading enzymes of vascular wilt fungi. II. Properties and modes of action of polysaccharidases of Verticilliwn albo-atrum and Fusarium oxysporum f.sp. lycopersici. Physiol Plant Pathol 13: 101–134CrossRefGoogle Scholar
- Cooper RM, Longman D, Campbell A, Henry M and Lees PE (1988) Enzymic adaptation of cereal pathogens to the monocotyledonous primary wall. Physiol Molec Plant Pathol 32: 33–47CrossRefGoogle Scholar
- Davis KR, Lyon GD, Darvill AG and Alberheim P (1984) Host-pathogen interactions XXV. Endopolygalacturonic acid lyase from Erwinia carotovora elicits phytoalexin accumulation by releasing plant cell wall fragments. Plant Physiol 74: 52–60PubMedCrossRefGoogle Scholar
- Dickerson AG, Mantle PG, Nisbet LJ and Shaw BI (1978) A role for β-glucanases in the parasitism of cereals by Claviceps purpurea. Physiol Plant Pathol 12: 55–62CrossRefGoogle Scholar
- Durrands PK and Cooper RM (1988) Selection and characterization of pectinase deficient mutants of the vascular wilt pathogen Verticillium ablo-atrum. Physiol Molec Plant Pathol 32: 343–362CrossRefGoogle Scholar
- Durrands PK, Keene RA, Cooper RM, O’Garro LW and Clarkson JM (1988) Poly-galacturonase isozyme profiles from Verticilliwn dahliae isolates races 1 and 2 from different geographical origins. Trans Br mycol Soc 91: 533–535CrossRefGoogle Scholar
- Halverson LJ and Stacey G (1986) Signal exchange in plant-microbe interactions. Microbial Rev 50: 193–225Google Scholar
- Hancock JG (1966) Degradation of pectic substances associated with pathogenesis by Sclerotinia sclerotiorum in sunflower and tomato stems. Phytopathology 56: 975–9Google Scholar
- Hatfield RD and Nevins DJ (1987) Hydrolytic activity and substrate specificity of an endoglucanase from Zea mays seedling cell walls. Plant Physiol 83: 203–207PubMedCrossRefGoogle Scholar
- Highley TL, Wolter KE and Evans FJ (1981) Polysaccharide-degrading complex produced in wood and in liquid media by the brown-rot fungus Poria placenta. Wood and Fibre 13: 265–274Google Scholar
- Hislop EC, Keon JPR and Fielding AH (1979) Effect of pectin lyase from Monilinia fructigena on viability, ultrastructure and localization of acid phosphatase of cultured apple cells. Physiol Plant Pathol 14: 371–81CrossRefGoogle Scholar
- Howell, HE (1975) Correlation of virulence with secretion in vitro of three wall-degrading enzymes in isolates of Sclerotinia fructigena obtained after mutagen treatment. J Gen Microbiol 90: 32–40PubMedGoogle Scholar
- Ishii S (1984) Cell wall cementing materials of grass leaves. Plant Physiol 76: 959–961PubMedCrossRefGoogle Scholar
- Jarvis MC, Threlfall DR and Friend J (1981) Potato cell wall poly-saccharides: degradation with enzymes from Phytophthora infestons. J. Exp Bot 32: 1309–1319CrossRefGoogle Scholar
- Keen NT, Dahlbeck D, Staskawicz B and Belser W (1984) Molecular cloning of pec täte lyase genes from Erwinia chrysanthemi and their expression in Escherichiacoli. J Bacteriol 159: 825–831PubMedGoogle Scholar
- Keon JPR (1985) Cytological damage and cell wall modification in cultured apple cells following exposure to pectin lyase from Monilinia fructigena. Physiol Plant Pathol 26: 11–29CrossRefGoogle Scholar
- Keon JPR, Byrde RJW and Cooper RM (1987) Some aspects of fungal enzymes that degrade plant cell walls. In: Pegg GF and Ayres PG (eds) Fungal infection in plants. Cambridge University Press, pp 133–157Google Scholar
- Knee M (1978) Properties of polygalacturonate and cell cohesion in apple fruit cortical tissue. Phytochem 17: 1257–1260CrossRefGoogle Scholar
- Knee M, Fielding AH, Archer SA and Laborda F (1975) Enzymic analysis of cell wall structure in apple fruit cortical tissue. Phytochem 14: 2213–2222CrossRefGoogle Scholar
- Lamed R, Setter E and Bayer EA (1983) Characterization of a cellulose-binding, cellulase-containing complex in Clostridium thermocellum. J Bacteriol 156: 828–836PubMedGoogle Scholar
- Lumsden RD (1969) Sclerotinia sclerotiorum infection of bean and the production of cellulase. Phytopathology 59: 653–657Google Scholar
- Mansfield JW and Richardson A (1981) The ultrastructure of interactions between Botrytis species and broad bean leaves. Physiol Plant Pathol 19: 41–8Google Scholar
- McClendon JH (1979) Subterminal polygalacturonase, a nonmacerating enzyme attacks pectate from the reducing end. Plant Physiol 63: 75–78CrossRefGoogle Scholar
- McNeil M, Darvill AG, Fry SC and Albersheim P (1984) Structure and function of the primary cell walls of plants. Ann Rev Biochem 53: 625–663PubMedCrossRefGoogle Scholar
- Nothnagel E, McNeil M, Albersheim P and Dell A (1983) Host pathogen interactions. XXII. A galacturonic acid oligosaccharide from plant cell walls elicits phytoalexins. Plant Physiol 71: 916–26PubMedCrossRefGoogle Scholar
- Pesis E, Fuchs Y and Zauberman G (1978) Cellulase activity and fruit softening in avocado. Plant Physiol 61: 416–419PubMedCrossRefGoogle Scholar
- Roeder DL and Collmer A (1985) Marker exchange mutagenesis of a pectate lyase isozyme gene from Erwinia chrysanthemi. J Bacteriol 164: 51–56PubMedGoogle Scholar
- Ryan CA, Bishop P, Pearce G, Darvill AG, McNeil M and Albersheim P (1981) A sycamore cell wall polysaccharide and a chemically related tomato leaf oligosaccharide possess similar proteinase inhibitor inducing activities. Plant Physiol 68: 616–18PubMedCrossRefGoogle Scholar
- Sexton R and Hall JL (1974) Fine structure and cytochemistry of the abscission zone of Phaseolus leaves. I. Ultrastructural changes occurring during abscission. Ann Bot 38: 849–854Google Scholar
- Sheiman MI, Macmillan JD, Miller K and Chase T (1976) Coordinated action of pectines terase and polygalacturonate lyase complex of Clostridium muhifermenians. Eur J Biochem 64: 565–572PubMedCrossRefGoogle Scholar
- Verhoeff K and Liem JI (1978) Presence of endo-polygalacturonase in conidia of Botrytis cinerea before and during germination. Phytopathol Z 91: 110–115CrossRefGoogle Scholar
- Wijesundera RLC, Bailey JA and Byrde RJW (1984) Production of pectin lyase by Colleiotrichwn lindemuthianum in culture and in infected bean (Phaseolus vulgaris) tissue. J Gen Microbiol 130: 285–290Google Scholar
- Willetts HJ, Byrde RJW and Fielding AH (1977) The taxonomy of the brown rot fungi (Monilinia spp) related to their extracellular wall-degrading enzymes. J Gen Microbiol 103: 77–83Google Scholar
- Wood TM and McCrae SI (1979) Synergism between enzymes involved in the solubilization of native cellulose. In: Brown RD and Jurasek L (eds) Advances in Chemistry, vol 181. Hydrolysis of cellulose: mechanisms of enzymatic and acid catalysis. American Chemical Society, pp 181–209Google Scholar
- Yamazaki N, Fry SC, Darvill AG and Albersheim P (1983) Host-pathogen interactions. XXIV. Fragments isolated from suspension-cultured sycamore cell walls inhibit the ability of cells to incorporate 14C-leucine into proteins. Plant Physiol 72: 864–9PubMedCrossRefGoogle Scholar
- Youle D and Cooper RM (1987) Possible determinants of pathogenicity of Erwinia amylovora: evidence for an induced toxin. Acta Hort 217: 161–166Google Scholar
- Zucker M and Hankin L (1970) Regulation of pectate lyase synthesis in Pseudomonas fluorescens and Erwinia carotovora. J Bacteriol 104: 13–18PubMedGoogle Scholar
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