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Production and characterization of a novel antifungal chitinase identified by functional screening of a suppressive-soil metagenome

BACKGROUND: Through functional screening of a fosmid library, generated from a phytopathogen-suppressive soil metagenome, the novel antifungal chitinase—named Chi18H8 and belonging to family 18 glycosyl hydrolases—was previously discovered. The initial extremely low yield of Chi18H8 recombinant prod...

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Autores principales: Berini, Francesca, Presti, Ilaria, Beltrametti, Fabrizio, Pedroli, Marco, Vårum, Kjell M., Pollegioni, Loredano, Sjöling, Sara, Marinelli, Flavia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282697/
https://www.ncbi.nlm.nih.gov/pubmed/28137256
http://dx.doi.org/10.1186/s12934-017-0634-8
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author Berini, Francesca
Presti, Ilaria
Beltrametti, Fabrizio
Pedroli, Marco
Vårum, Kjell M.
Pollegioni, Loredano
Sjöling, Sara
Marinelli, Flavia
author_facet Berini, Francesca
Presti, Ilaria
Beltrametti, Fabrizio
Pedroli, Marco
Vårum, Kjell M.
Pollegioni, Loredano
Sjöling, Sara
Marinelli, Flavia
author_sort Berini, Francesca
collection PubMed
description BACKGROUND: Through functional screening of a fosmid library, generated from a phytopathogen-suppressive soil metagenome, the novel antifungal chitinase—named Chi18H8 and belonging to family 18 glycosyl hydrolases—was previously discovered. The initial extremely low yield of Chi18H8 recombinant production and purification from Escherichia coli cells (21 μg/g cell) limited its characterization, thus preventing further investigation on its biotechnological potential. RESULTS: We report on how we succeeded in producing hundreds of milligrams of pure and biologically active Chi18H8 by developing and scaling up to a high-yielding, 30 L bioreactor process, based on a novel method of mild solubilization of E. coli inclusion bodies in lactic acid aqueous solution, coupled with a single step purification by hydrophobic interaction chromatography. Chi18H8 was characterized as a Ca(2+)-dependent mesophilic chitobiosidase, active on chitin substrates at acidic pHs and possessing interesting features, such as solvent tolerance, long-term stability in acidic environment and antifungal activity against the phytopathogens Fusarium graminearum and Rhizoctonia solani. Additionally, Chi18H8 was found to operate according to a non-processive endomode of action on a water-soluble chitin-like substrate. CONCLUSIONS: Expression screening of a metagenomic library may allow access to the functional diversity of uncultivable microbiota and to the discovery of novel enzymes useful for biotechnological applications. A persisting bottleneck, however, is the lack of methods for large scale production of metagenome-sourced enzymes from genes of unknown origin in the commonly used microbial hosts. To our knowledge, this is the first report on a novel metagenome-sourced enzyme produced in hundreds-of-milligram amount by recovering the protein in the biologically active form from recombinant E. coli inclusion bodies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-017-0634-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-52826972017-02-03 Production and characterization of a novel antifungal chitinase identified by functional screening of a suppressive-soil metagenome Berini, Francesca Presti, Ilaria Beltrametti, Fabrizio Pedroli, Marco Vårum, Kjell M. Pollegioni, Loredano Sjöling, Sara Marinelli, Flavia Microb Cell Fact Research BACKGROUND: Through functional screening of a fosmid library, generated from a phytopathogen-suppressive soil metagenome, the novel antifungal chitinase—named Chi18H8 and belonging to family 18 glycosyl hydrolases—was previously discovered. The initial extremely low yield of Chi18H8 recombinant production and purification from Escherichia coli cells (21 μg/g cell) limited its characterization, thus preventing further investigation on its biotechnological potential. RESULTS: We report on how we succeeded in producing hundreds of milligrams of pure and biologically active Chi18H8 by developing and scaling up to a high-yielding, 30 L bioreactor process, based on a novel method of mild solubilization of E. coli inclusion bodies in lactic acid aqueous solution, coupled with a single step purification by hydrophobic interaction chromatography. Chi18H8 was characterized as a Ca(2+)-dependent mesophilic chitobiosidase, active on chitin substrates at acidic pHs and possessing interesting features, such as solvent tolerance, long-term stability in acidic environment and antifungal activity against the phytopathogens Fusarium graminearum and Rhizoctonia solani. Additionally, Chi18H8 was found to operate according to a non-processive endomode of action on a water-soluble chitin-like substrate. CONCLUSIONS: Expression screening of a metagenomic library may allow access to the functional diversity of uncultivable microbiota and to the discovery of novel enzymes useful for biotechnological applications. A persisting bottleneck, however, is the lack of methods for large scale production of metagenome-sourced enzymes from genes of unknown origin in the commonly used microbial hosts. To our knowledge, this is the first report on a novel metagenome-sourced enzyme produced in hundreds-of-milligram amount by recovering the protein in the biologically active form from recombinant E. coli inclusion bodies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-017-0634-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-31 /pmc/articles/PMC5282697/ /pubmed/28137256 http://dx.doi.org/10.1186/s12934-017-0634-8 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Berini, Francesca
Presti, Ilaria
Beltrametti, Fabrizio
Pedroli, Marco
Vårum, Kjell M.
Pollegioni, Loredano
Sjöling, Sara
Marinelli, Flavia
Production and characterization of a novel antifungal chitinase identified by functional screening of a suppressive-soil metagenome
title Production and characterization of a novel antifungal chitinase identified by functional screening of a suppressive-soil metagenome
title_full Production and characterization of a novel antifungal chitinase identified by functional screening of a suppressive-soil metagenome
title_fullStr Production and characterization of a novel antifungal chitinase identified by functional screening of a suppressive-soil metagenome
title_full_unstemmed Production and characterization of a novel antifungal chitinase identified by functional screening of a suppressive-soil metagenome
title_short Production and characterization of a novel antifungal chitinase identified by functional screening of a suppressive-soil metagenome
title_sort production and characterization of a novel antifungal chitinase identified by functional screening of a suppressive-soil metagenome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282697/
https://www.ncbi.nlm.nih.gov/pubmed/28137256
http://dx.doi.org/10.1186/s12934-017-0634-8
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