Purificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)
Autor(a) principal: | |
---|---|
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 |
id |
UFRN_dfd8546b53519c108fb4be4736efc66d |
---|---|
oai_identifier_str |
oai:https://repositorio.ufrn.br:123456789/12544 |
network_acronym_str |
UFRN |
network_name_str |
Repositório Institucional da UFRN |
repository_id_str |
|
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 |
dc.date.accessioned.fl_str_mv |
2014-12-17T14:03:30Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
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. |
url |
https://repositorio.ufrn.br/jspui/handle/123456789/12544 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal do Rio Grande do Norte |
dc.publisher.program.fl_str_mv |
Programa de Pós-Graduação em Bioquímica |
dc.publisher.initials.fl_str_mv |
UFRN |
dc.publisher.country.fl_str_mv |
BR |
dc.publisher.department.fl_str_mv |
Bioquímica; Biologia Molecular |
publisher.none.fl_str_mv |
Universidade Federal do Rio Grande do Norte |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFRN instname:Universidade Federal do Rio Grande do Norte (UFRN) instacron:UFRN |
instname_str |
Universidade Federal do Rio Grande do Norte (UFRN) |
instacron_str |
UFRN |
institution |
UFRN |
reponame_str |
Repositório Institucional da UFRN |
collection |
Repositório Institucional da UFRN |
bitstream.url.fl_str_mv |
https://repositorio.ufrn.br/bitstream/123456789/12544/6/AnaCBC.pdf.txt https://repositorio.ufrn.br/bitstream/123456789/12544/8/PurificacaoCaracterizacaoAn%c3%a1lise_Cruz_2008.pdf.txt https://repositorio.ufrn.br/bitstream/123456789/12544/7/AnaCBC.pdf.jpg https://repositorio.ufrn.br/bitstream/123456789/12544/9/PurificacaoCaracterizacaoAn%c3%a1lise_Cruz_2008.pdf.jpg https://repositorio.ufrn.br/bitstream/123456789/12544/1/PurificacaoCaracterizacaoAn%c3%a1lise_Cruz_2008.pdf |
bitstream.checksum.fl_str_mv |
52f2e0ce466a55fd29e4062ba244ca51 52f2e0ce466a55fd29e4062ba244ca51 3bb93a5139ee60cd99137ab17907ecae 3bb93a5139ee60cd99137ab17907ecae 881b82ecb0df2b87414957a1e02761bb |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN) |
repository.mail.fl_str_mv |
|
_version_ |
1814832657643601920 |