Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)

Detalhes bibliográficos
Autor(a) principal: Cruz, Ana Celly Bezerra
Data de Publicação: 2008
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/jspui/handle/123456789/12544
Resumo: One Kunitz-type trypsin inhibitors (PmTI) was purified from Piptadenia moniliformis seeds, a tree of the sub-family Mimosoideae, by TCA precipitation, affinity chromatography on immobilized trypsin-Sepharose, DEAE cellulose (ion exchange) and Superose 12 (molecular exclusion) column FPLC/AKTA. The inhibitor has Mr of 25 kDa by SDS-PAGE and chromatography molecular exclusion. The N-terminal sequence of this inhibitor showed high homology with other family Kunitz inhibitors. This also stable variations in temperature and pH and showed a small decrease in its activity when incubated with DDT in the concentration of 100mM for 120 minutes. The inhibition of trypsin by PmTI was competitive, with Ki of 1.57 x10-11 M. The activity of trypsin was effectively inhibited by percentage of inhibition of 100%, among enzymes tested, was not detected inhibition for the bromelain, was weak inhibitor of pancreatic elastase (3.17% of inhibition) and inhibited by 76.42% elastase of neutrophils, and inhibited in a moderate, chymotrypsin and papain with percentage of inhibition of 42.96% and 23.10% respectively. In vitro assays against digestive proteinases from Lepidoptera, Diptera and Coleoptera pests were carried out. Several degrees of inhibition were found. For Anthonomus grandis and Ceratitis capitata the inhibition was 89.93% and 70.52%, respectively, and the enzymes of Zabrotes subfasciatus and Callosobruchus maculatus were inhibited by 5.96% and 9.41%, respectively, and the enzymes of Plodia. interpunctella and Castnia licus were inhibited by 59.94% and 23.67, respectively. In vivo assays, was observed reduction in the development of larvae in 4rd instar of C. capitata, when PmTI was added to the artificial diet, getting WD50 and LD50 of 0.30% and 0.33%, respectively. These results suggest that this inhibitor could be a strong candidate to plant management programs cross transgenic
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spelling Cruz, Ana Celly Bezerrahttp://lattes.cnpq.br/6635163328842232http://lattes.cnpq.br/7890362793618911Oliveira, Antônia Elenir Amânciohttp://lattes.cnpq.br/2207461519012659Matta, Luciana Duarte Martins dahttp://lattes.cnpq.br/2752887804614967Santos, Elizeu Antunes doshttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4782221T9&dataRevisao=nullSales, Maurício Pereira de2014-12-17T14:03:30Z2009-05-142014-12-17T14:03:30Z2008-10-20CRUZ, Ana Celly Bezerra. Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis). 2008. 100 f. Dissertação (Mestrado em Bioquímica; Biologia Molecular) - Universidade Federal do Rio Grande do Norte, Natal, 2008.https://repositorio.ufrn.br/jspui/handle/123456789/12544One Kunitz-type trypsin inhibitors (PmTI) was purified from Piptadenia moniliformis seeds, a tree of the sub-family Mimosoideae, by TCA precipitation, affinity chromatography on immobilized trypsin-Sepharose, DEAE cellulose (ion exchange) and Superose 12 (molecular exclusion) column FPLC/AKTA. The inhibitor has Mr of 25 kDa by SDS-PAGE and chromatography molecular exclusion. The N-terminal sequence of this inhibitor showed high homology with other family Kunitz inhibitors. This also stable variations in temperature and pH and showed a small decrease in its activity when incubated with DDT in the concentration of 100mM for 120 minutes. The inhibition of trypsin by PmTI was competitive, with Ki of 1.57 x10-11 M. The activity of trypsin was effectively inhibited by percentage of inhibition of 100%, among enzymes tested, was not detected inhibition for the bromelain, was weak inhibitor of pancreatic elastase (3.17% of inhibition) and inhibited by 76.42% elastase of neutrophils, and inhibited in a moderate, chymotrypsin and papain with percentage of inhibition of 42.96% and 23.10% respectively. In vitro assays against digestive proteinases from Lepidoptera, Diptera and Coleoptera pests were carried out. Several degrees of inhibition were found. For Anthonomus grandis and Ceratitis capitata the inhibition was 89.93% and 70.52%, respectively, and the enzymes of Zabrotes subfasciatus and Callosobruchus maculatus were inhibited by 5.96% and 9.41%, respectively, and the enzymes of Plodia. interpunctella and Castnia licus were inhibited by 59.94% and 23.67, respectively. In vivo assays, was observed reduction in the development of larvae in 4rd instar of C. capitata, when PmTI was added to the artificial diet, getting WD50 and LD50 of 0.30% and 0.33%, respectively. These results suggest that this inhibitor could be a strong candidate to plant management programs cross transgenicUm inibidor de tripsina da família Kunitz (PmTI) foi purificado de sementes de Piptadenia moniliformis, uma árvore da sub-família Mimosoideae, através da precipitação com ácido tricloroacético (TCA), cromatografia de afinidade com tripsina acoplada em sepharose, coluna DEAE- celulose(troca iônica) e Superose 12 (exclusão molecular) em sistema FPLC/AKTA. O inibidor possui massa molecular de 25 kDa como confirmado através de SDS-PAGE e cromatografia de exclusão molecular. A seqüência do N-terminal deste inibidor mostrou alta homologia com outros inibidores da família Kunitz. Este também é estável as variações de temperatura e pH, e apresentou um pequeno decréscimo na sua atividade quando incubado com DTT na concentração de 100 mM por 120 minutos. A inibição da tripsina foi do tipo competitiva com Ki de 1,57x10-11 mM. A atividade da tripsina foi inibida efetivamente com percentual de inibição de 100%, entre as outras enzimas testadas não foi detectada inibição para a bromelaína, foi fracamente inibidor da elastase pancreática (3,17% de inibição), inibiu em 76,42% elastase de neutrófilos, inibiu de forma moderada quimotripsina e papaína com percentual de inibição de 42,96% e 23,10%, respectivamente. Ensaios in vitro foram realizados com as proteinases digestivas de Lepidóptera, Coleóptera e Díptera. Vários graus de inibição foram encontrados. Para Anthonomus grandis e Ceratitis capitata a inibição foi de 89,93% e 70,52%, respectivamente, e as enzimas de Zabrotes subfasciatus e Callosobruchus maculatus foram inibidas com percentuais de 5,96% e 9,41% respectivamente, e as enzimas de Plodia interpunctella e Castnia licus foram inibidas com percentuais de 59,94% e 23,67%, respectivamente. No ensaio in vivo, foi observada redução no desenvolvimento de larvas em 4º ínstar de C. capitata, quando PmTI foi adicionado à dieta artificial, obtendo WD50 de 0,30% e LD50 0,33% . Estes resultados sugerem que este inibidor possa ser um forte candidato para programas de melhoramentos de plantas via transgeniaapplication/pdfporUniversidade Federal do Rio Grande do NortePrograma de Pós-Graduação em BioquímicaUFRNBRBioquímica; Biologia MolecularInibidor de tripsinaPiptadenia moniliformisInsetos pragaBioinseticidaInibidor KunitzTrypsin inhibitorPiptadenia moniliformisInsect pestsBioinsecticideKunitz inhibitorCNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICAPurificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNTEXTAnaCBC.pdf.txtAnaCBC.pdf.txtExtracted texttext/plain147255https://repositorio.ufrn.br/bitstream/123456789/12544/6/AnaCBC.pdf.txt52f2e0ce466a55fd29e4062ba244ca51MD56PurificacaoCaracterizacaoAnálise_Cruz_2008.pdf.txtPurificacaoCaracterizacaoAnálise_Cruz_2008.pdf.txtExtracted texttext/plain147255https://repositorio.ufrn.br/bitstream/123456789/12544/8/PurificacaoCaracterizacaoAn%c3%a1lise_Cruz_2008.pdf.txt52f2e0ce466a55fd29e4062ba244ca51MD58THUMBNAILAnaCBC.pdf.jpgAnaCBC.pdf.jpgIM Thumbnailimage/jpeg3208https://repositorio.ufrn.br/bitstream/123456789/12544/7/AnaCBC.pdf.jpg3bb93a5139ee60cd99137ab17907ecaeMD57PurificacaoCaracterizacaoAnálise_Cruz_2008.pdf.jpgPurificacaoCaracterizacaoAnálise_Cruz_2008.pdf.jpgIM Thumbnailimage/jpeg3208https://repositorio.ufrn.br/bitstream/123456789/12544/9/PurificacaoCaracterizacaoAn%c3%a1lise_Cruz_2008.pdf.jpg3bb93a5139ee60cd99137ab17907ecaeMD59ORIGINALPurificacaoCaracterizacaoAnálise_Cruz_2008.pdfapplication/pdf1320381https://repositorio.ufrn.br/bitstream/123456789/12544/1/PurificacaoCaracterizacaoAn%c3%a1lise_Cruz_2008.pdf881b82ecb0df2b87414957a1e02761bbMD51123456789/125442019-01-29 16:48:52.985oai:https://repositorio.ufrn.br:123456789/12544Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2019-01-29T19:48:52Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false
dc.title.por.fl_str_mv Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)
title Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)
spellingShingle Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)
Cruz, Ana Celly Bezerra
Inibidor de tripsina
Piptadenia moniliformis
Insetos praga
Bioinseticida
Inibidor Kunitz
Trypsin inhibitor
Piptadenia moniliformis
Insect pests
Bioinsecticide
Kunitz inhibitor
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
title_short Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)
title_full Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)
title_fullStr Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)
title_full_unstemmed Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)
title_sort Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)
author Cruz, Ana Celly Bezerra
author_facet Cruz, Ana Celly Bezerra
author_role author
dc.contributor.authorID.por.fl_str_mv
dc.contributor.authorLattes.por.fl_str_mv http://lattes.cnpq.br/6635163328842232
dc.contributor.advisorID.por.fl_str_mv
dc.contributor.advisorLattes.por.fl_str_mv http://lattes.cnpq.br/7890362793618911
dc.contributor.referees1.pt_BR.fl_str_mv Oliveira, Antônia Elenir Amâncio
dc.contributor.referees1ID.por.fl_str_mv
dc.contributor.referees1Lattes.por.fl_str_mv http://lattes.cnpq.br/2207461519012659
dc.contributor.referees2.pt_BR.fl_str_mv Matta, Luciana Duarte Martins da
dc.contributor.referees2ID.por.fl_str_mv
dc.contributor.referees2Lattes.por.fl_str_mv http://lattes.cnpq.br/2752887804614967
dc.contributor.referees3.pt_BR.fl_str_mv Santos, Elizeu Antunes dos
dc.contributor.referees3ID.por.fl_str_mv
dc.contributor.referees3Lattes.por.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4782221T9&dataRevisao=null
dc.contributor.author.fl_str_mv Cruz, Ana Celly Bezerra
dc.contributor.advisor1.fl_str_mv Sales, Maurício Pereira de
contributor_str_mv Sales, Maurício Pereira de
dc.subject.por.fl_str_mv Inibidor de tripsina
Piptadenia moniliformis
Insetos praga
Bioinseticida
Inibidor Kunitz
topic Inibidor de tripsina
Piptadenia moniliformis
Insetos praga
Bioinseticida
Inibidor Kunitz
Trypsin inhibitor
Piptadenia moniliformis
Insect pests
Bioinsecticide
Kunitz inhibitor
CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
dc.subject.eng.fl_str_mv Trypsin inhibitor
Piptadenia moniliformis
Insect pests
Bioinsecticide
Kunitz inhibitor
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA
description One Kunitz-type trypsin inhibitors (PmTI) was purified from Piptadenia moniliformis seeds, a tree of the sub-family Mimosoideae, by TCA precipitation, affinity chromatography on immobilized trypsin-Sepharose, DEAE cellulose (ion exchange) and Superose 12 (molecular exclusion) column FPLC/AKTA. The inhibitor has Mr of 25 kDa by SDS-PAGE and chromatography molecular exclusion. The N-terminal sequence of this inhibitor showed high homology with other family Kunitz inhibitors. This also stable variations in temperature and pH and showed a small decrease in its activity when incubated with DDT in the concentration of 100mM for 120 minutes. The inhibition of trypsin by PmTI was competitive, with Ki of 1.57 x10-11 M. The activity of trypsin was effectively inhibited by percentage of inhibition of 100%, among enzymes tested, was not detected inhibition for the bromelain, was weak inhibitor of pancreatic elastase (3.17% of inhibition) and inhibited by 76.42% elastase of neutrophils, and inhibited in a moderate, chymotrypsin and papain with percentage of inhibition of 42.96% and 23.10% respectively. In vitro assays against digestive proteinases from Lepidoptera, Diptera and Coleoptera pests were carried out. Several degrees of inhibition were found. For Anthonomus grandis and Ceratitis capitata the inhibition was 89.93% and 70.52%, respectively, and the enzymes of Zabrotes subfasciatus and Callosobruchus maculatus were inhibited by 5.96% and 9.41%, respectively, and the enzymes of Plodia. interpunctella and Castnia licus were inhibited by 59.94% and 23.67, respectively. In vivo assays, was observed reduction in the development of larvae in 4rd instar of C. capitata, when PmTI was added to the artificial diet, getting WD50 and LD50 of 0.30% and 0.33%, respectively. These results suggest that this inhibitor could be a strong candidate to plant management programs cross transgenic
publishDate 2008
dc.date.issued.fl_str_mv 2008-10-20
dc.date.available.fl_str_mv 2009-05-14
2014-12-17T14:03:30Z
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dc.identifier.citation.fl_str_mv CRUZ, Ana Celly Bezerra. Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis). 2008. 100 f. Dissertação (Mestrado em Bioquímica; Biologia Molecular) - Universidade Federal do Rio Grande do Norte, Natal, 2008.
dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/jspui/handle/123456789/12544
identifier_str_mv CRUZ, Ana Celly Bezerra. Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis). 2008. 100 f. Dissertação (Mestrado em Bioquímica; Biologia Molecular) - Universidade Federal do Rio Grande do Norte, Natal, 2008.
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