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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Autor principal: Wolski, E.A
Otros Autores: Lima, C., Agusti, R., Daleo, G.R, Andreu, A.B, De Lederkremer, R.M
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2005
Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
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024 7 |2 scopus  |a 2-s2.0-13844321254 
024 7 |2 cas  |a 1,3 beta glucanase, 9073-49-8; glucan 1,4 alpha glucosidase, 9032-08-0; glucan, 9012-72-0, 9037-91-6; Glucan Endo-1,3-beta-D-Glucosidase, EC 3.2.1.39; Glucans 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a CRBRA 
100 1 |a Wolski, E.A. 
245 1 3 |a An α-glucan elicitor from the cell wall of a biocontrol binucleate Rhizoctonia isolate 
260 |c 2005 
270 1 0 |m De Lederkremer, R.M.; CIHIDECAR-CONICET, Depto. de Quím. Orgán., Ciudad Universitaria, PO Box 1428, Buenos Aires, Argentina; email: lederk@qo.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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504 |a Carbonero, E.R., Sassaki, G.L., Stuelp, P.M., Gorin, P.A.J., Woranovicz-Barreira, S.M., Iacomini, M., (2001) FEMS Microbiol. Lett., 194, pp. 65-69 
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520 3 |a 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.  |l eng 
536 |a Detalles de la financiación: Universidad Nacional de Mar del Plata 
536 |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica, PICT 06-05133 
536 |a Detalles de la financiación: Universidad de Buenos Aires 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: This research was supported by the Universidad Nacional de Mar del Plata, the Universidad de Buenos Aires, the Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) and Agencia Nacional de Promoción Científica y Tecnológica (ANPCYT, PICT 06-05133). GRD is researcher of Comisión de Investigaciones Científicas de la Provincia de Buenos Aires (CIC) and RML is researcher of Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). 
593 |a Inst. de Invest. Biológicas, Fac. de Ciencias Exactas Y Naturales, Univ. Nacional de Mar del Plata, PO Box 1245, Buenos Aires, Argentina 
593 |a CIHIDECAR-CONICET, Depto. de Quím. Orgán., Ciudad Universitaria, PO Box 1428, Buenos Aires, Argentina 
690 1 0 |a Α-GLUCAN 
690 1 0 |a Β-1,3 GLUCANASE INDUCTION 
690 1 0 |a BINUCLEATE RHIZOCTONIA 
690 1 0 |a ELICITOR 
690 1 0 |a BACTERIA 
690 1 0 |a CELLS 
690 1 0 |a CHROMATOGRAPHIC ANALYSIS 
690 1 0 |a DEGRADATION 
690 1 0 |a DISEASES 
690 1 0 |a HYDROLYSIS 
690 1 0 |a NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY 
690 1 0 |a PH EFFECTS 
690 1 0 |a PLANT CELL CULTURE 
690 1 0 |a BIOCONTROL AGENTS 
690 1 0 |a HYDROLYTIC ENZYMES 
690 1 0 |a MICROBIAL INFECTION 
690 1 0 |a RHIZOCTONIA CANKER 
690 1 0 |a ENZYMES 
690 1 0 |a 1,3 BETA GLUCANASE 
690 1 0 |a ALPHA GLUCAN 
690 1 0 |a GLUCAN 
690 1 0 |a GLUCAN 1,4 ALPHA GLUCOSIDASE 
690 1 0 |a PHYTOALEXIN 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a URONIC ACID 
690 1 0 |a ANION EXCHANGE CHROMATOGRAPHY 
690 1 0 |a ARTICLE 
690 1 0 |a CELL WALL 
690 1 0 |a CORRELATION ANALYSIS 
690 1 0 |a ENZYME ACTIVITY 
690 1 0 |a ENZYME INDUCTION 
690 1 0 |a FUNGAL CELL 
690 1 0 |a HYPHOMYCETES 
690 1 0 |a METHYLATION 
690 1 0 |a MYCELIUM 
690 1 0 |a NONHUMAN 
690 1 0 |a NUCLEAR MAGNETIC RESONANCE 
690 1 0 |a POTATO 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a CELL WALL 
690 1 0 |a ENZYME INDUCTION 
690 1 0 |a GLUCAN ENDO-1,3-BETA-D-GLUCOSIDASE 
690 1 0 |a GLUCANS 
690 1 0 |a KINETICS 
690 1 0 |a METHYLATION 
690 1 0 |a NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR 
690 1 0 |a PEST CONTROL, BIOLOGICAL 
690 1 0 |a RHIZOCTONIA 
690 1 0 |a RHIZOCTONIA 
690 1 0 |a SOLANUM TUBEROSUM 
690 1 0 |a THANATEPHORUS CUCUMERIS 
700 1 |a Lima, C. 
700 1 |a Agusti, R. 
700 1 |a Daleo, G.R. 
700 1 |a Andreu, A.B. 
700 1 |a De Lederkremer, R.M. 
773 0 |d 2005  |g v. 340  |h pp. 619-627  |k n. 4  |p Carbohydr. Res.  |x 00086215  |w (AR-BaUEN)CENRE-301  |t Carbohydrate Research 
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