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Characterization of a protease produced by a Trichoderma harzianum isolate which controls cocoa plant witches' broom disease

BACKGROUND: Several Trichoderma strains have been reported to be effective in controlling plant diseases, and the action of fungal hydrolytic enzymes has been considered as the main mechanism involved in the antagonistic process. However, although Trichoderma strains were found to impair development...

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Autores principales: De Marco, Janice L, Felix, Carlos Roberto
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC65675/
https://www.ncbi.nlm.nih.gov/pubmed/11835696
http://dx.doi.org/10.1186/1471-2091-3-3
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author De Marco, Janice L
Felix, Carlos Roberto
author_facet De Marco, Janice L
Felix, Carlos Roberto
author_sort De Marco, Janice L
collection PubMed
description BACKGROUND: Several Trichoderma strains have been reported to be effective in controlling plant diseases, and the action of fungal hydrolytic enzymes has been considered as the main mechanism involved in the antagonistic process. However, although Trichoderma strains were found to impair development of Crinipellis perniciosa, the causal agent of cocoa plant witches' broom disease, no fungal strain is available for effective control of this disease. We have then undertaken a program of construction of hydrolytic enzyme-overproducing Trichoderma strains aiming improvement of the fungal antagonistic capacity. The protease of an indian Trichoderma isolate showing antagonistic activity against C. perniciosa was purified to homogeneity and characterized for its kinetic properties and action on the phytopathogen cell wall. RESULTS: A protease produced by the Trichoderma harzianum isolate 1051 was purified to homogeneity by precipitation with ammonium sulfate followed by hydrophobic chromatography. The molecular mass of this protease as determined by SDS-polyacrylamide gel electrophoresis was about 18.8 kDa. Its N-terminal amino acid sequence shares no homology with any other protease. The purified enzyme substantially affected the cell wall of the phytopathogen C. perniciosa. Western-blotting analysis showed that the enzyme was present in the culture supernatant 24 h after the Trichoderma started to grow in casein-containing liquid medium. CONCLUSIONS: The capacity of the Trichoderma harzianum protease to hydrolyze the cell wall of C. perniciosa indicates that this enzyme may be actually involved in the antagonistic process between the two fungi. This fact strongly suggest that hydrolytic enzyme over-producing transgenic fungi may show superior biocontrol capacity.
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spelling pubmed-656752002-02-25 Characterization of a protease produced by a Trichoderma harzianum isolate which controls cocoa plant witches' broom disease De Marco, Janice L Felix, Carlos Roberto BMC Biochem Methodology Article BACKGROUND: Several Trichoderma strains have been reported to be effective in controlling plant diseases, and the action of fungal hydrolytic enzymes has been considered as the main mechanism involved in the antagonistic process. However, although Trichoderma strains were found to impair development of Crinipellis perniciosa, the causal agent of cocoa plant witches' broom disease, no fungal strain is available for effective control of this disease. We have then undertaken a program of construction of hydrolytic enzyme-overproducing Trichoderma strains aiming improvement of the fungal antagonistic capacity. The protease of an indian Trichoderma isolate showing antagonistic activity against C. perniciosa was purified to homogeneity and characterized for its kinetic properties and action on the phytopathogen cell wall. RESULTS: A protease produced by the Trichoderma harzianum isolate 1051 was purified to homogeneity by precipitation with ammonium sulfate followed by hydrophobic chromatography. The molecular mass of this protease as determined by SDS-polyacrylamide gel electrophoresis was about 18.8 kDa. Its N-terminal amino acid sequence shares no homology with any other protease. The purified enzyme substantially affected the cell wall of the phytopathogen C. perniciosa. Western-blotting analysis showed that the enzyme was present in the culture supernatant 24 h after the Trichoderma started to grow in casein-containing liquid medium. CONCLUSIONS: The capacity of the Trichoderma harzianum protease to hydrolyze the cell wall of C. perniciosa indicates that this enzyme may be actually involved in the antagonistic process between the two fungi. This fact strongly suggest that hydrolytic enzyme over-producing transgenic fungi may show superior biocontrol capacity. BioMed Central 2002-01-22 /pmc/articles/PMC65675/ /pubmed/11835696 http://dx.doi.org/10.1186/1471-2091-3-3 Text en Copyright © 2002 De Marco and Felix; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Methodology Article
De Marco, Janice L
Felix, Carlos Roberto
Characterization of a protease produced by a Trichoderma harzianum isolate which controls cocoa plant witches' broom disease
title Characterization of a protease produced by a Trichoderma harzianum isolate which controls cocoa plant witches' broom disease
title_full Characterization of a protease produced by a Trichoderma harzianum isolate which controls cocoa plant witches' broom disease
title_fullStr Characterization of a protease produced by a Trichoderma harzianum isolate which controls cocoa plant witches' broom disease
title_full_unstemmed Characterization of a protease produced by a Trichoderma harzianum isolate which controls cocoa plant witches' broom disease
title_short Characterization of a protease produced by a Trichoderma harzianum isolate which controls cocoa plant witches' broom disease
title_sort characterization of a protease produced by a trichoderma harzianum isolate which controls cocoa plant witches' broom disease
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC65675/
https://www.ncbi.nlm.nih.gov/pubmed/11835696
http://dx.doi.org/10.1186/1471-2091-3-3
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