Literature DB >> 16661404

Glycosidic Enzyme Activity in Pea Tissue and Pea-Fusarium solani Interactions.

E J Nichols1, J M Beckman, L A Hadwiger.   

Abstract

Membrane barriers which prevent direct contact between Fusarium solani and pea endocarp tissue prevent fungal spores from inducing phytoalexin production. Conversely, preinduced host resistance responses are not readily transported from the plant across the membrane barrier to Fusarium macroconidia.Crude enzyme extracts from pea endocarp tissues partially degrade Fusarium solani f. sp. phaseoli cell walls. Activities of the glycosidic enzymes, chitinase, beta-1,3-glucanase, chitosanase, beta-D-N-acetylglucosaminidase, beta-D-N-acetylgalactosaminidase, beta-D-glucosidase, alpha-D-glucosidase, and alpha-D-mannosidase, were detected in pea endocarp tissue. If pods are challenged with Fusarium spores or chitosan, the chitinase activity of the infected tissue remains higher than water-treated pods 0.5 to 6 hours after treatment. The beta-1,3-glucanase activity increases within 6 hours in both inoculated and control tissue. Chitosanase activity was lower in tissue treated with Fusarium solani f. sp. pisi, f. sp. phaseoli or chitosan than in water-treated control tissue. Thus, the pea tissue contains glycosidic enzymes with the potential to degrade the major compounds of the Fusarium cell walls.

Entities:  

Year:  1980        PMID: 16661404      PMCID: PMC440565          DOI: 10.1104/pp.66.2.199

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  13 in total

1.  Deficient uridine diphosphate-N-acetylglucosamine:glycoprotein N-acetylglucosaminyltransferase activity in a clone of Chinese hamster ovary cells with altered surface glycoproteins.

Authors:  C Gottlieb; J Baenziger; S Kornfeld
Journal:  J Biol Chem       Date:  1975-05-10       Impact factor: 5.157

2.  STUDIES ON THE CHITINASE SYSTEM IN BEAN AND OTHER SEEDS.

Authors:  R F POWNING; H IRZYKIEWICZ
Journal:  Comp Biochem Physiol       Date:  1965-01

3.  The determination of glucosamine and galactosamine.

Authors:  C J RONDLE; W T MORGAN
Journal:  Biochem J       Date:  1955-12       Impact factor: 3.857

4.  Physiological and Cytological Similarities between Disease Resistance and Cellular Incompatibility Responses.

Authors:  J Teasdale; D Daniels; W C Davis; R Eddy; L A Hadwiger
Journal:  Plant Physiol       Date:  1974-11       Impact factor: 8.340

5.  A colorimetric method for the determination of N-acetylglucosamine and N-acetylchrondrosamine.

Authors:  W T Morgan; L A Elson
Journal:  Biochem J       Date:  1934       Impact factor: 3.857

6.  Glycosidases of Phaseolus vulgaris. I. Isolation and characterization of beta-N-acetylglucosaminidase.

Authors:  O P Bahl; K M Agrawal
Journal:  J Biol Chem       Date:  1968-01-10       Impact factor: 5.157

7.  Isolation and characterization of fig lysozyme.

Authors:  A N Glazer; A O Barel; J B Howard; D M Brown
Journal:  J Biol Chem       Date:  1969-07-10       Impact factor: 5.157

8.  Increase in linolenic Acid is not a prerequisite for development of freezing tolerance in wheat.

Authors:  A I de la Roche
Journal:  Plant Physiol       Date:  1979-01       Impact factor: 8.340

9.  Temporal and hormonal control of beta-1,3-glucanase in Phaseolus vulgaris L.

Authors:  F B Abeles; L E Forrence
Journal:  Plant Physiol       Date:  1970-04       Impact factor: 8.340

10.  Histones of Neurospora crassa.

Authors:  C G Goff
Journal:  J Biol Chem       Date:  1976-07-10       Impact factor: 5.157

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  16 in total

1.  Regulation of a chitinase gene promoter by ethylene and elicitors in bean protoplasts.

Authors:  D Roby; K Broglie; J Gaynor; R Broglie
Journal:  Plant Physiol       Date:  1991-09       Impact factor: 8.340

2.  The disease resistance response in pea is associated with increased levels of specific mRNAs.

Authors:  R C Riggleman; B Fristensky; L A Hadwiger
Journal:  Plant Mol Biol       Date:  1985-03       Impact factor: 4.076

3.  Plant gene expression in response to pathogens.

Authors:  D B Collinge; A J Slusarenko
Journal:  Plant Mol Biol       Date:  1987-07       Impact factor: 4.076

4.  Proteinase inhibitor synthesis in tomato leaves : induction by chitosan oligomers and chemically modified chitosan and chitin.

Authors:  M Walker-Simmons; C A Ryan
Journal:  Plant Physiol       Date:  1984-11       Impact factor: 8.340

5.  Differential effects of elicitors on the viability of rice suspension cells.

Authors:  C Masuta; M Van den Bulcke; G Bauw; M Van Montagu; A B Caplan
Journal:  Plant Physiol       Date:  1991-10       Impact factor: 8.340

6.  Comparison of proteinase inhibitor-inducing activities and phytoalexin elicitor activities of a pure fungal endopolygalacturonase, pectic fragments, and chitosans.

Authors:  M Walker-Simmons; D Jin; C A West; L Hadwiger; C A Ryan
Journal:  Plant Physiol       Date:  1984-11       Impact factor: 8.340

7.  Cell Surfaces in Plant-Microorganism Interactions : VI. Elicitors of Ethylene from Colletotrichum lagenarium Trigger Chitinase Activity in Melon Plants.

Authors:  D Roby; A Toppan; M T Esquerré-Tugayé
Journal:  Plant Physiol       Date:  1986-05       Impact factor: 8.340

8.  Induced chitinase activity in resistant wheat leaves inoculated with an incompatible race of Puccinia striiformis f. sp. tritici, the causal agent of yellow rust disease.

Authors:  Mojtaba Mohammadi; Râmin Roohparvar; Mohammad Torabi
Journal:  Mycopathologia       Date:  2002       Impact factor: 2.574

9.  Induction, purification and characterization of chitinase isolated from pea leaves inoculated with Ascochyta pisi.

Authors:  K Vad; J D Mikkelsen; D B Collinge
Journal:  Planta       Date:  1991-04       Impact factor: 4.116

10.  Chitinase in bean leaves: induction by ethylene, purification, properties, and possible function.

Authors:  T Boller; A Gehri; F Mauch; U Vögeli
Journal:  Planta       Date:  1983-02       Impact factor: 4.116

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