Jaburetox-2Ec: An insecticidal peptide derived from an: isoform of urease from the plant canavalia ensiformis

Detalhes bibliográficos
Autor(a) principal: Mulinari, Fernanda Fontana
Data de Publicação: 2007
Outros Autores: Stanisçuaski, Fernanda, Bertholdo-Vargas, Lúcia R., Postal, Melissa, Oliveira-Neto, Osmundo Brilhante de, Rigden, Daniel Jonh, Grossi-de-Sá, Maria de Fátima, Carlini, Celia Regina
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UCB
Texto Completo: http://twingo.ucb.br:8080/jspui/handle/10869/672
https://repositorio.ucb.br:9443/jspui/handle/123456789/7923
Resumo: Canatoxin, a urease isoform from Canavalia ensiformis seeds, shows insecticidal activity against different insect species. Its toxicity relies on an internal 10 kDa peptide (pepcanatox), released by hydrolysis of Canatoxin by cathepsins in the digestive system of susceptible insects. In the present work, based on the N-terminal sequence of pepcanatox, we have designed primers to amplify by PCR a 270-bp fragment corresponding to pepcanatox using JBURE-II cDNA (one of the urease isoforms cloned from C. ensiformis, with high identity to JBURE-I, the classical urease) as a template. This amplicon named jaburetox-2 was cloned into pET 101 vector to obtain heterologous expression in Escherichia coli of the recombinant protein in C-terminal fusion with V-5 epitope and 6-His tag. Jaburetox-2Ec was purified on Nickel-NTA resin and bioassayed in insect models. Dysdercus peruvianus larvae were fed on cotton seed meal diets containing 0.01% (w/w) Jaburetox-2Ec and, after 11 days, all individuals were dead. Jaburetox-2Ec was also tested against Spodoptera frugiperda larvae and caused 100% mortality. In contrast, high doses of Jaburetox-2Ec were innocuous when injected or ingested by mice and neonate rats. Modeling of Jaburetox-2Ec, in comparison with other peptide structures, revealed a prominent b-hairpin motif consistent with an insecticidal activity based on either neurotoxicity or cell permeation.
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spelling Mulinari, Fernanda FontanaStanisçuaski, FernandaBertholdo-Vargas, Lúcia R.Postal, MelissaOliveira-Neto, Osmundo Brilhante deRigden, Daniel JonhGrossi-de-Sá, Maria de FátimaCarlini, Celia Regina2016-10-10T03:53:07Z2016-10-10T03:53:07Z2007-08MULINARI, Fernanda Fontana, et al. Jaburetox-2Ec: an insecticidal peptide derived from an: isoform of urease from the plant Canavalia ensiformis. Peptides, v. 28, p. 2042- 2050, 2007.http://twingo.ucb.br:8080/jspui/handle/10869/672https://repositorio.ucb.br:9443/jspui/handle/123456789/7923Canatoxin, a urease isoform from Canavalia ensiformis seeds, shows insecticidal activity against different insect species. Its toxicity relies on an internal 10 kDa peptide (pepcanatox), released by hydrolysis of Canatoxin by cathepsins in the digestive system of susceptible insects. In the present work, based on the N-terminal sequence of pepcanatox, we have designed primers to amplify by PCR a 270-bp fragment corresponding to pepcanatox using JBURE-II cDNA (one of the urease isoforms cloned from C. ensiformis, with high identity to JBURE-I, the classical urease) as a template. This amplicon named jaburetox-2 was cloned into pET 101 vector to obtain heterologous expression in Escherichia coli of the recombinant protein in C-terminal fusion with V-5 epitope and 6-His tag. Jaburetox-2Ec was purified on Nickel-NTA resin and bioassayed in insect models. Dysdercus peruvianus larvae were fed on cotton seed meal diets containing 0.01% (w/w) Jaburetox-2Ec and, after 11 days, all individuals were dead. Jaburetox-2Ec was also tested against Spodoptera frugiperda larvae and caused 100% mortality. In contrast, high doses of Jaburetox-2Ec were innocuous when injected or ingested by mice and neonate rats. Modeling of Jaburetox-2Ec, in comparison with other peptide structures, revealed a prominent b-hairpin motif consistent with an insecticidal activity based on either neurotoxicity or cell permeation.Made available in DSpace on 2016-10-10T03:53:07Z (GMT). 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dc.title.pt_BR.fl_str_mv Jaburetox-2Ec: An insecticidal peptide derived from an: isoform of urease from the plant canavalia ensiformis
title Jaburetox-2Ec: An insecticidal peptide derived from an: isoform of urease from the plant canavalia ensiformis
spellingShingle Jaburetox-2Ec: An insecticidal peptide derived from an: isoform of urease from the plant canavalia ensiformis
Mulinari, Fernanda Fontana
Canatoxin
Insecticide
Spodoptera frugiperda
Dysdercus peruvianus
Molecular modeling
Heterologous expression
title_short Jaburetox-2Ec: An insecticidal peptide derived from an: isoform of urease from the plant canavalia ensiformis
title_full Jaburetox-2Ec: An insecticidal peptide derived from an: isoform of urease from the plant canavalia ensiformis
title_fullStr Jaburetox-2Ec: An insecticidal peptide derived from an: isoform of urease from the plant canavalia ensiformis
title_full_unstemmed Jaburetox-2Ec: An insecticidal peptide derived from an: isoform of urease from the plant canavalia ensiformis
title_sort Jaburetox-2Ec: An insecticidal peptide derived from an: isoform of urease from the plant canavalia ensiformis
author Mulinari, Fernanda Fontana
author_facet Mulinari, Fernanda Fontana
Stanisçuaski, Fernanda
Bertholdo-Vargas, Lúcia R.
Postal, Melissa
Oliveira-Neto, Osmundo Brilhante de
Rigden, Daniel Jonh
Grossi-de-Sá, Maria de Fátima
Carlini, Celia Regina
author_role author
author2 Stanisçuaski, Fernanda
Bertholdo-Vargas, Lúcia R.
Postal, Melissa
Oliveira-Neto, Osmundo Brilhante de
Rigden, Daniel Jonh
Grossi-de-Sá, Maria de Fátima
Carlini, Celia Regina
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Mulinari, Fernanda Fontana
Stanisçuaski, Fernanda
Bertholdo-Vargas, Lúcia R.
Postal, Melissa
Oliveira-Neto, Osmundo Brilhante de
Rigden, Daniel Jonh
Grossi-de-Sá, Maria de Fátima
Carlini, Celia Regina
dc.subject.por.fl_str_mv Canatoxin
Insecticide
Spodoptera frugiperda
Dysdercus peruvianus
Molecular modeling
Heterologous expression
topic Canatoxin
Insecticide
Spodoptera frugiperda
Dysdercus peruvianus
Molecular modeling
Heterologous expression
dc.description.abstract.por.fl_txt_mv Canatoxin, a urease isoform from Canavalia ensiformis seeds, shows insecticidal activity against different insect species. Its toxicity relies on an internal 10 kDa peptide (pepcanatox), released by hydrolysis of Canatoxin by cathepsins in the digestive system of susceptible insects. In the present work, based on the N-terminal sequence of pepcanatox, we have designed primers to amplify by PCR a 270-bp fragment corresponding to pepcanatox using JBURE-II cDNA (one of the urease isoforms cloned from C. ensiformis, with high identity to JBURE-I, the classical urease) as a template. This amplicon named jaburetox-2 was cloned into pET 101 vector to obtain heterologous expression in Escherichia coli of the recombinant protein in C-terminal fusion with V-5 epitope and 6-His tag. Jaburetox-2Ec was purified on Nickel-NTA resin and bioassayed in insect models. Dysdercus peruvianus larvae were fed on cotton seed meal diets containing 0.01% (w/w) Jaburetox-2Ec and, after 11 days, all individuals were dead. Jaburetox-2Ec was also tested against Spodoptera frugiperda larvae and caused 100% mortality. In contrast, high doses of Jaburetox-2Ec were innocuous when injected or ingested by mice and neonate rats. Modeling of Jaburetox-2Ec, in comparison with other peptide structures, revealed a prominent b-hairpin motif consistent with an insecticidal activity based on either neurotoxicity or cell permeation.
dc.description.version.pt_BR.fl_txt_mv Sim
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description Canatoxin, a urease isoform from Canavalia ensiformis seeds, shows insecticidal activity against different insect species. Its toxicity relies on an internal 10 kDa peptide (pepcanatox), released by hydrolysis of Canatoxin by cathepsins in the digestive system of susceptible insects. In the present work, based on the N-terminal sequence of pepcanatox, we have designed primers to amplify by PCR a 270-bp fragment corresponding to pepcanatox using JBURE-II cDNA (one of the urease isoforms cloned from C. ensiformis, with high identity to JBURE-I, the classical urease) as a template. This amplicon named jaburetox-2 was cloned into pET 101 vector to obtain heterologous expression in Escherichia coli of the recombinant protein in C-terminal fusion with V-5 epitope and 6-His tag. Jaburetox-2Ec was purified on Nickel-NTA resin and bioassayed in insect models. Dysdercus peruvianus larvae were fed on cotton seed meal diets containing 0.01% (w/w) Jaburetox-2Ec and, after 11 days, all individuals were dead. Jaburetox-2Ec was also tested against Spodoptera frugiperda larvae and caused 100% mortality. In contrast, high doses of Jaburetox-2Ec were innocuous when injected or ingested by mice and neonate rats. Modeling of Jaburetox-2Ec, in comparison with other peptide structures, revealed a prominent b-hairpin motif consistent with an insecticidal activity based on either neurotoxicity or cell permeation.
publishDate 2007
dc.date.issued.fl_str_mv 2007-08
dc.date.accessioned.fl_str_mv 2016-10-10T03:53:07Z
dc.date.available.fl_str_mv 2016-10-10T03:53:07Z
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dc.identifier.citation.fl_str_mv MULINARI, Fernanda Fontana, et al. Jaburetox-2Ec: an insecticidal peptide derived from an: isoform of urease from the plant Canavalia ensiformis. Peptides, v. 28, p. 2042- 2050, 2007.
dc.identifier.uri.fl_str_mv http://twingo.ucb.br:8080/jspui/handle/10869/672
https://repositorio.ucb.br:9443/jspui/handle/123456789/7923
identifier_str_mv MULINARI, Fernanda Fontana, et al. Jaburetox-2Ec: an insecticidal peptide derived from an: isoform of urease from the plant Canavalia ensiformis. Peptides, v. 28, p. 2042- 2050, 2007.
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