Purification of a killer toxin from Aureobasidium pullulans for the biocontrol of phytopathogens

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MetadadosDescriçãoIdioma
Autor(es): dc.contributorUniversidade Estadual Paulista (Unesp)-
Autor(es): dc.contributorUniv Ctr Herminio Ometto Fdn FHO-
Autor(es): dc.contributorSylvio Moreira Citriculture Ctr IAC-
Autor(es): dc.creatorMoura, Vanessa S. [UNESP]-
Autor(es): dc.creatorPollettini, Flavia L. [UNESP]-
Autor(es): dc.creatorFerraz, Luriany P. [UNESP]-
Autor(es): dc.creatorMazzi, Mauricio V.-
Autor(es): dc.creatorKupper, Katia C. [UNESP]-
Data de aceite: dc.date.accessioned2022-02-22T00:55:14Z-
Data de disponibilização: dc.date.available2022-02-22T00:55:14Z-
Data de envio: dc.date.issued2021-06-25-
Data de envio: dc.date.issued2021-06-25-
Data de envio: dc.date.issued2020-12-28-
Fonte completa do material: dc.identifierhttp://dx.doi.org/10.1002/jobm.202000164-
Fonte completa do material: dc.identifierhttp://hdl.handle.net/11449/209052-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/11449/209052-
Descrição: dc.descriptionThe objectives of the present study were to purify and assess the killer toxin effect produced by Aureobasidium pullulans under casual agents of green mold (Penicillum digitatum) and sour rot (Geotrichum citri-aurantii). Initially, different methods of protein precipitation were tested. The proteolytic activity and the presence of proteins acting on cell wall receptors, beta-1,3-glucanase and chitinase were determined, and toxin purification was conducted by Sephadex G-75 gel exclusion chromatography and cellulose chromatography (medium fibers). Subsequently, purification was confirmed by polyacrylamide gel electrophoresis, and the detection of killer activity was performed in solid YEPD-methylene blue buffered with citrate-phosphate (0.1 M, pH 4.6). Toxin identification was performed by liquid chromatography-mass spectrometry. The results showed that the best protein precipitation method was 2:1 ethanol (vol/vol ethanol/supernatant). It was possible to observe the presence of enzymes with proteolytic activity, including beta-1,3-glucanase and chitinase. During the purification process, it was verified that the killer toxin produced by the yeast has a low-molecular-weight protein belonging to the ubiquitin family, which presents killer activity against P. digitatum and G. citri-aurantii.-
Descrição: dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
Descrição: dc.descriptionJulio de Mesquita Filho Paulista State Univ, Grad Agr Microbiol Program, Agr & Veterinarian Fac, Sao Paulo, Brazil-
Descrição: dc.descriptionUniv Ctr Herminio Ometto Fdn FHO, Grad Program Biomed Sci, Sao Paulo, Brazil-
Descrição: dc.descriptionSylvio Moreira Citriculture Ctr IAC, Rodovia Anhanguera,Km 158,CP 04, BR-13470970 Cordeiropolis, SP, Brazil-
Descrição: dc.descriptionJulio de Mesquita Filho Paulista State Univ, Grad Agr Microbiol Program, Agr & Veterinarian Fac, Sao Paulo, Brazil-
Descrição: dc.descriptionFAPESP: 2014/25067-3-
Formato: dc.format77-87-
Idioma: dc.languageen-
Publicador: dc.publisherWiley-Blackwell-
Relação: dc.relationJournal Of Basic Microbiology-
???dc.source???: dc.sourceWeb of Science-
Palavras-chave: dc.subjectGeotrichum citri&#8208-
Palavras-chave: dc.subjectaurantii-
Palavras-chave: dc.subjecthydrolytic enzymes-
Palavras-chave: dc.subjectPenicillium digitatum-
Palavras-chave: dc.subjectubiquitin&#8208-
Palavras-chave: dc.subjectlike-
Título: dc.titlePurification of a killer toxin from Aureobasidium pullulans for the biocontrol of phytopathogens-
Tipo de arquivo: dc.typelivro digital-
Aparece nas coleções:Repositório Institucional - Unesp

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