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Chitinolytic Enzymes of the Hyperparasite Fungus Aphanocladium album: Genome-Wide Survey and Characterization of A Selected Enzyme

The filamentous fungus Aphanocladium album is known as a hyperparasite of plant pathogenic fungi; hence, it has been studied as a possible agent for plant protection. Chitinases secreted by A. album have proven to be essential for its fungicidal activity. However, no complete analysis of the A. albu...

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Autores principales: Leoni, Claudia, Manzari, Caterina, Chiara, Matteo, Veronico, Pasqua, Bruno, Giovanni Luigi, Pesole, Graziano, Ceci, Luigi R., Volpicella, Mariateresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223446/
https://www.ncbi.nlm.nih.gov/pubmed/37317333
http://dx.doi.org/10.3390/microorganisms11051357
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author Leoni, Claudia
Manzari, Caterina
Chiara, Matteo
Veronico, Pasqua
Bruno, Giovanni Luigi
Pesole, Graziano
Ceci, Luigi R.
Volpicella, Mariateresa
author_facet Leoni, Claudia
Manzari, Caterina
Chiara, Matteo
Veronico, Pasqua
Bruno, Giovanni Luigi
Pesole, Graziano
Ceci, Luigi R.
Volpicella, Mariateresa
author_sort Leoni, Claudia
collection PubMed
description The filamentous fungus Aphanocladium album is known as a hyperparasite of plant pathogenic fungi; hence, it has been studied as a possible agent for plant protection. Chitinases secreted by A. album have proven to be essential for its fungicidal activity. However, no complete analysis of the A. album chitinase assortment has been carried out, nor have any of its chitinases been characterized yet. In this study, we report the first draft assembly of the genome sequence of A. album (strain MX-95). The in silico functional annotation of the genome allowed the identification of 46 genes encoding chitinolytic enzymes of the GH18 (26 genes), GH20 (8 genes), GH75 (8 genes), and GH3 (4 genes) families. The encoded proteins were investigated by comparative and phylogenetic analysis, allowing clustering in different subgroups. A. album chitinases were also characterized according to the presence of different functional protein domains (carbohydrate-binding modules and catalytic domains) providing the first complete description of the chitinase repertoire of A. album. A single chitinase gene was then selected for complete functional characterization. The encoded protein was expressed in the yeast Pichia pastoris, and its activity was assayed under different conditions of temperature and pH and with different substrates. It was found that the enzyme acts mainly as a chitobiosidase, with higher activity in the 37–50 °C range.
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spelling pubmed-102234462023-05-28 Chitinolytic Enzymes of the Hyperparasite Fungus Aphanocladium album: Genome-Wide Survey and Characterization of A Selected Enzyme Leoni, Claudia Manzari, Caterina Chiara, Matteo Veronico, Pasqua Bruno, Giovanni Luigi Pesole, Graziano Ceci, Luigi R. Volpicella, Mariateresa Microorganisms Article The filamentous fungus Aphanocladium album is known as a hyperparasite of plant pathogenic fungi; hence, it has been studied as a possible agent for plant protection. Chitinases secreted by A. album have proven to be essential for its fungicidal activity. However, no complete analysis of the A. album chitinase assortment has been carried out, nor have any of its chitinases been characterized yet. In this study, we report the first draft assembly of the genome sequence of A. album (strain MX-95). The in silico functional annotation of the genome allowed the identification of 46 genes encoding chitinolytic enzymes of the GH18 (26 genes), GH20 (8 genes), GH75 (8 genes), and GH3 (4 genes) families. The encoded proteins were investigated by comparative and phylogenetic analysis, allowing clustering in different subgroups. A. album chitinases were also characterized according to the presence of different functional protein domains (carbohydrate-binding modules and catalytic domains) providing the first complete description of the chitinase repertoire of A. album. A single chitinase gene was then selected for complete functional characterization. The encoded protein was expressed in the yeast Pichia pastoris, and its activity was assayed under different conditions of temperature and pH and with different substrates. It was found that the enzyme acts mainly as a chitobiosidase, with higher activity in the 37–50 °C range. MDPI 2023-05-22 /pmc/articles/PMC10223446/ /pubmed/37317333 http://dx.doi.org/10.3390/microorganisms11051357 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Leoni, Claudia
Manzari, Caterina
Chiara, Matteo
Veronico, Pasqua
Bruno, Giovanni Luigi
Pesole, Graziano
Ceci, Luigi R.
Volpicella, Mariateresa
Chitinolytic Enzymes of the Hyperparasite Fungus Aphanocladium album: Genome-Wide Survey and Characterization of A Selected Enzyme
title Chitinolytic Enzymes of the Hyperparasite Fungus Aphanocladium album: Genome-Wide Survey and Characterization of A Selected Enzyme
title_full Chitinolytic Enzymes of the Hyperparasite Fungus Aphanocladium album: Genome-Wide Survey and Characterization of A Selected Enzyme
title_fullStr Chitinolytic Enzymes of the Hyperparasite Fungus Aphanocladium album: Genome-Wide Survey and Characterization of A Selected Enzyme
title_full_unstemmed Chitinolytic Enzymes of the Hyperparasite Fungus Aphanocladium album: Genome-Wide Survey and Characterization of A Selected Enzyme
title_short Chitinolytic Enzymes of the Hyperparasite Fungus Aphanocladium album: Genome-Wide Survey and Characterization of A Selected Enzyme
title_sort chitinolytic enzymes of the hyperparasite fungus aphanocladium album: genome-wide survey and characterization of a selected enzyme
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223446/
https://www.ncbi.nlm.nih.gov/pubmed/37317333
http://dx.doi.org/10.3390/microorganisms11051357
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