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dc.contributor.author
Díaz, María Eugenia
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Rocha, Gabriela Fernanda
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Kise, Francisco
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Rosso, A. M.
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Guevara, Maria Gabriela
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Parisi, M.G.
dc.date.available
2019-10-28T17:12:56Z
dc.date.issued
2018-04-24
dc.identifier.citation
Díaz, María Eugenia; Rocha, Gabriela Fernanda; Kise, Francisco; Rosso, A. M.; Guevara, Maria Gabriela; et al.; Antimicrobial activity of an aspartic protease from Salpichroa origanifolia fruits; Wiley Blackwell Publishing, Inc; Letters in Applied Microbiology; 67; 2; 24-4-2018; 168-174
dc.identifier.issn
0266-8254
dc.identifier.uri
http://hdl.handle.net/11336/87396
dc.description.abstract
Abstract: Plant proteases play a fundamental role in several processes like growth, development and in response to biotic and abiotic stress. In particular, aspartic proteases (AP) are expressed in different plant organs and have antimicrobial activity. Previously, we purified an AP from Salpichroa origanifolia fruits called salpichroin. The aim of this work was to determine the cytotoxic activity of this enzyme on selected plant and human pathogens. For this purpose, the growth of the selected pathogens was analysed after exposure to different concentrations of salpichroin. The results showed that the enzyme was capable of inhibiting Fusarium solani and Staphylococcus aureus in a dose-dependent manner. It was determined that 1·2 μmol l−1 of salpichroin was necessary to inhibit 50% of conidial germination, and the minimal bactericidal concentration was between 1·9 and 2·5 μmol l−1. Using SYTOX Green dye we were able to demonstrate that salpichroin cause membrane permeabilization. Moreover, the enzyme treated with its specific inhibitor pepstatin A did not lose its antibacterial activity. This finding demonstrates that the cytotoxic activity of salpichroin is due to the alteration of the cell plasma membrane barrier but not due to its proteolytic activity. Antimicrobial activity of the AP could represent a potential alternative for the control of pathogens that affect humans or crops of economic interest. Significance and Impact of the Study: This study provides insights into the antimicrobial activity of an aspartic protease isolated from Salpichroa origanifolia fruits on plant and human pathogens. The proteinase inhibited Fusarium solani and Staphylococcus aureus in a dose-dependent manner due to the alteration of the cell plasma membrane barrier but not due to its proteolytic activity. Antimicrobial activity of salpichroin suggests its potential applications as an important tool for the control of pathogenic micro-organisms affecting humans and crops of economic interest. Therefore, it would represent a new alternative to avoid the problems of environmental pollution and antimicrobial resistance.
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application/pdf
dc.language.iso
eng
dc.publisher
Wiley Blackwell Publishing, Inc
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
antimicrobials
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cytotoxicity
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fungi
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proteinase
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Staphylococci
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Biología Celular, Microbiología
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Ciencias Biológicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Antimicrobial activity of an aspartic protease from Salpichroa origanifolia fruits
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info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2019-10-22T15:49:44Z
dc.journal.volume
67
dc.journal.number
2
dc.journal.pagination
168-174
dc.journal.pais
Reino Unido
dc.journal.ciudad
Londres
dc.description.fil
Fil: Díaz, María Eugenia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Luján; Argentina
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Fil: Rocha, Gabriela Fernanda. Universidad Nacional de Luján; Argentina
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Fil: Kise, Francisco. Universidad Nacional de Luján; Argentina
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Fil: Rosso, A. M.. Universidad Nacional de Luján; Argentina
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Fil: Guevara, Maria Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones Biológicas. Universidad Nacional de Mar del Plata. Facultad de Ciencias Exactas y Naturales. Instituto de Investigaciones Biológicas; Argentina
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Fil: Parisi, M.G.. Universidad Nacional de Luján; Argentina
dc.journal.title
Letters in Applied Microbiology
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pubmed/29740840
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1111/lam.13006
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