An α-glucan elicitor from the cell wall of a biocontrol binucleate Rhizoctonia isolate

Binucleate Rhizoctonia (BNR) isolate (232-C6) is an effective biocontrol agent for protection of potato from Rhizoctonia canker, a disease caused by Rhizoctonia solani. Production of hydrolytic enzymes is one of the best known inducible defense responses following microbial infection. We isolated an...

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Autores principales: Agustí, Rosalía, Daleo, Gustavo Raúl, Muchnik de Lederkremer, Rosa María
Publicado: 2005
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v340_n4_p619_Wolski
http://hdl.handle.net/20.500.12110/paper_00086215_v340_n4_p619_Wolski
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spelling paper:paper_00086215_v340_n4_p619_Wolski2025-07-30T17:15:52Z An α-glucan elicitor from the cell wall of a biocontrol binucleate Rhizoctonia isolate Agustí, Rosalía Daleo, Gustavo Raúl Muchnik de Lederkremer, Rosa María α-glucan β-1,3 Glucanase induction Binucleate Rhizoctonia Elicitor Bacteria Cells Chromatographic analysis Degradation Diseases Hydrolysis Nuclear magnetic resonance spectroscopy pH effects Plant cell culture Biocontrol agents Hydrolytic enzymes Microbial infection Rhizoctonia canker Enzymes 1,3 beta glucanase alpha glucan glucan glucan 1,4 alpha glucosidase phytoalexin unclassified drug uronic acid anion exchange chromatography article cell wall correlation analysis enzyme activity enzyme induction fungal cell Hyphomycetes methylation mycelium nonhuman nuclear magnetic resonance potato priority journal Cell Wall Enzyme Induction Glucan Endo-1,3-beta-D-Glucosidase Glucans Kinetics Methylation Nuclear Magnetic Resonance, Biomolecular Pest Control, Biological Rhizoctonia Rhizoctonia Solanum tuberosum Thanatephorus cucumeris Binucleate Rhizoctonia (BNR) isolate (232-C6) is an effective biocontrol agent for protection of potato from Rhizoctonia canker, a disease caused by Rhizoctonia solani. Production of hydrolytic enzymes is one of the best known inducible defense responses following microbial infection. We isolated and characterized a cell wall α-glucan from BNR, which induces β-1,3 glucanase activities in potato sprouts, the primary site of infection by R. solani. An autoclaving method, previously reported for isolation of oligosaccharide elicitors was used, and the glucan purified by chromatographic techniques. Maximal induction of β-1,3 glucanase activity in potato sprouts was obtained with 250 μg of the α-glucan elicitor after 6 days from inoculation time. Both, BNR mycelium and the α-glucan produced a similar kinetic response of β-1,3 glucanase. However, the α-glucan did not induce phytoalexin accumulation, previously correlated with the defense response. Uronic acids (∼10% with respect to total neutral sugars) were determined and identified as glucuronic acid by high-pH anion-exchange chromatography. Methylation analysis showed that the glucan consists of (1→3) and (1→4)-linked glucose units with preponderance of the first ones. Some of the (1→4) linkages were branched at position 6. The glucan was partially degraded with amyloglucosidase. This, together with the NMR spectra data and the high optical rotation of the original (+195°) and degraded glucans (+175°) proved the α configuration. Further methylation of the amyloglucosidase degraded glucans indicated that they consist of (1→3)-linked glucoses. The present study is the first report on the isolation and characterization of an α-glucan from Rhizoctonia, that may be important as a biocontrol factor. © 2005 Elsevier Ltd. All rights reserved. Fil:Agusti, R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Daleo, G.R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:De Lederkremer, R.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2005 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v340_n4_p619_Wolski http://hdl.handle.net/20.500.12110/paper_00086215_v340_n4_p619_Wolski
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic α-glucan
β-1,3 Glucanase induction
Binucleate Rhizoctonia
Elicitor
Bacteria
Cells
Chromatographic analysis
Degradation
Diseases
Hydrolysis
Nuclear magnetic resonance spectroscopy
pH effects
Plant cell culture
Biocontrol agents
Hydrolytic enzymes
Microbial infection
Rhizoctonia canker
Enzymes
1,3 beta glucanase
alpha glucan
glucan
glucan 1,4 alpha glucosidase
phytoalexin
unclassified drug
uronic acid
anion exchange chromatography
article
cell wall
correlation analysis
enzyme activity
enzyme induction
fungal cell
Hyphomycetes
methylation
mycelium
nonhuman
nuclear magnetic resonance
potato
priority journal
Cell Wall
Enzyme Induction
Glucan Endo-1,3-beta-D-Glucosidase
Glucans
Kinetics
Methylation
Nuclear Magnetic Resonance, Biomolecular
Pest Control, Biological
Rhizoctonia
Rhizoctonia
Solanum tuberosum
Thanatephorus cucumeris
spellingShingle α-glucan
β-1,3 Glucanase induction
Binucleate Rhizoctonia
Elicitor
Bacteria
Cells
Chromatographic analysis
Degradation
Diseases
Hydrolysis
Nuclear magnetic resonance spectroscopy
pH effects
Plant cell culture
Biocontrol agents
Hydrolytic enzymes
Microbial infection
Rhizoctonia canker
Enzymes
1,3 beta glucanase
alpha glucan
glucan
glucan 1,4 alpha glucosidase
phytoalexin
unclassified drug
uronic acid
anion exchange chromatography
article
cell wall
correlation analysis
enzyme activity
enzyme induction
fungal cell
Hyphomycetes
methylation
mycelium
nonhuman
nuclear magnetic resonance
potato
priority journal
Cell Wall
Enzyme Induction
Glucan Endo-1,3-beta-D-Glucosidase
Glucans
Kinetics
Methylation
Nuclear Magnetic Resonance, Biomolecular
Pest Control, Biological
Rhizoctonia
Rhizoctonia
Solanum tuberosum
Thanatephorus cucumeris
Agustí, Rosalía
Daleo, Gustavo Raúl
Muchnik de Lederkremer, Rosa María
An α-glucan elicitor from the cell wall of a biocontrol binucleate Rhizoctonia isolate
topic_facet α-glucan
β-1,3 Glucanase induction
Binucleate Rhizoctonia
Elicitor
Bacteria
Cells
Chromatographic analysis
Degradation
Diseases
Hydrolysis
Nuclear magnetic resonance spectroscopy
pH effects
Plant cell culture
Biocontrol agents
Hydrolytic enzymes
Microbial infection
Rhizoctonia canker
Enzymes
1,3 beta glucanase
alpha glucan
glucan
glucan 1,4 alpha glucosidase
phytoalexin
unclassified drug
uronic acid
anion exchange chromatography
article
cell wall
correlation analysis
enzyme activity
enzyme induction
fungal cell
Hyphomycetes
methylation
mycelium
nonhuman
nuclear magnetic resonance
potato
priority journal
Cell Wall
Enzyme Induction
Glucan Endo-1,3-beta-D-Glucosidase
Glucans
Kinetics
Methylation
Nuclear Magnetic Resonance, Biomolecular
Pest Control, Biological
Rhizoctonia
Rhizoctonia
Solanum tuberosum
Thanatephorus cucumeris
description Binucleate Rhizoctonia (BNR) isolate (232-C6) is an effective biocontrol agent for protection of potato from Rhizoctonia canker, a disease caused by Rhizoctonia solani. Production of hydrolytic enzymes is one of the best known inducible defense responses following microbial infection. We isolated and characterized a cell wall α-glucan from BNR, which induces β-1,3 glucanase activities in potato sprouts, the primary site of infection by R. solani. An autoclaving method, previously reported for isolation of oligosaccharide elicitors was used, and the glucan purified by chromatographic techniques. Maximal induction of β-1,3 glucanase activity in potato sprouts was obtained with 250 μg of the α-glucan elicitor after 6 days from inoculation time. Both, BNR mycelium and the α-glucan produced a similar kinetic response of β-1,3 glucanase. However, the α-glucan did not induce phytoalexin accumulation, previously correlated with the defense response. Uronic acids (∼10% with respect to total neutral sugars) were determined and identified as glucuronic acid by high-pH anion-exchange chromatography. Methylation analysis showed that the glucan consists of (1→3) and (1→4)-linked glucose units with preponderance of the first ones. Some of the (1→4) linkages were branched at position 6. The glucan was partially degraded with amyloglucosidase. This, together with the NMR spectra data and the high optical rotation of the original (+195°) and degraded glucans (+175°) proved the α configuration. Further methylation of the amyloglucosidase degraded glucans indicated that they consist of (1→3)-linked glucoses. The present study is the first report on the isolation and characterization of an α-glucan from Rhizoctonia, that may be important as a biocontrol factor. © 2005 Elsevier Ltd. All rights reserved.
author Agustí, Rosalía
Daleo, Gustavo Raúl
Muchnik de Lederkremer, Rosa María
author_facet Agustí, Rosalía
Daleo, Gustavo Raúl
Muchnik de Lederkremer, Rosa María
author_sort Agustí, Rosalía
title An α-glucan elicitor from the cell wall of a biocontrol binucleate Rhizoctonia isolate
title_short An α-glucan elicitor from the cell wall of a biocontrol binucleate Rhizoctonia isolate
title_full An α-glucan elicitor from the cell wall of a biocontrol binucleate Rhizoctonia isolate
title_fullStr An α-glucan elicitor from the cell wall of a biocontrol binucleate Rhizoctonia isolate
title_full_unstemmed An α-glucan elicitor from the cell wall of a biocontrol binucleate Rhizoctonia isolate
title_sort α-glucan elicitor from the cell wall of a biocontrol binucleate rhizoctonia isolate
publishDate 2005
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v340_n4_p619_Wolski
http://hdl.handle.net/20.500.12110/paper_00086215_v340_n4_p619_Wolski
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