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The Fusarium graminearum cerato-platanins loosen cellulose substrates enhancing fungal cellulase activity as expansin-like proteins.
Quarantin, Alessandra; Castiglioni, Carla; Schäfer, Wilhelm; Favaron, Francesco; Sella, Luca.
Afiliação
  • Quarantin A; Department of Land, Environment, Agriculture and Forestry (TESAF), Research Group in Plant Pathology, Università degli Studi di Padova, Viale dell'Università 16, 35020, Legnaro, Italy.
  • Castiglioni C; Department of Land, Environment, Agriculture and Forestry (TESAF), Research Group in Plant Pathology, Università degli Studi di Padova, Viale dell'Università 16, 35020, Legnaro, Italy.
  • Schäfer W; Biocenter Klein Flottbek, Molecular Phytopathology and Genetics, University of Hamburg, Hamburg, Germany.
  • Favaron F; Department of Land, Environment, Agriculture and Forestry (TESAF), Research Group in Plant Pathology, Università degli Studi di Padova, Viale dell'Università 16, 35020, Legnaro, Italy.
  • Sella L; Department of Land, Environment, Agriculture and Forestry (TESAF), Research Group in Plant Pathology, Università degli Studi di Padova, Viale dell'Università 16, 35020, Legnaro, Italy. Electronic address: luca.sella@unipd.it.
Plant Physiol Biochem ; 139: 229-238, 2019 Jun.
Article em En | MEDLINE | ID: mdl-30913532
Cerato-platanin proteins (CPPs) are small non-catalytic, cysteine-rich hydrophobic proteins produced by filamentous fungi. The genome of Fusarium graminearum, the causal agent of Fusarium head blight disease of wheat and other cereal grains, contains two genes putatively encoding for CPPs. To better characterize their features, the two FgCPPs were heterologously expressed in Pichia pastoris. The recombinant FgCPPs reduced the viscosity of a cellulose soluble derivate (carboxymethyl cellulose, CMC). The same effect was not observed on other polysaccharide substrates such as chitin, 1,3-ß-glucan, xylan and pectin. Indeed, differently from other fungal CPPs and similarly to expansins, FgCPPs are trapped by cellulose and not by chitin, thus suggesting that these proteins interact with cellulose. A double knock-out mutant deleted of both FgCPPs encoding genes produces much more cellulase activity than the corresponding wild type strain when grown on CMC, likely compensating the absence of FgCPPs. This result prompted us to investigate a possible synergistic effect of these proteins with fungal cellulases. The incubation of FgCPPs in the presence of a fungal cellulase (EC 3.2.1.4) determines an increased enzymatic activity on CMC, filter paper and wheat cell walls. The observation that FgCPPs act with a non-hydrolytic mechanism indicates that these proteins favor fungal cellulase activity in an expansin-like manner. Though the disruption of the FgCPP genes had no demonstrable impact on fungal virulence, our experimental data suggest their probable involvement in virulence, thus we refer to them as accessory virulence genes. Our results suggest also that the FgCPPs could be exploited for future biotechnological application in second-generation biofuels production on lignocellulosic biomasses rich in cellulose. Finally, we demonstrate that FgCPPs act as elicitors of defense responses on Arabidopsis leaves, increasing resistance to Botrytis cinerea infections.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Fúngicas / Parede Celular / Celulose / Plumbaginaceae / Fusarium Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Fúngicas / Parede Celular / Celulose / Plumbaginaceae / Fusarium Idioma: En Ano de publicação: 2019 Tipo de documento: Article