dc.contributorSales, Maurício Pereira de
dc.contributor
dc.contributorhttp://lattes.cnpq.br/6635163328842232
dc.contributor
dc.contributorhttp://lattes.cnpq.br/7890362793618911
dc.contributorOliveira, Antônia Elenir Amâncio
dc.contributor
dc.contributorhttp://lattes.cnpq.br/2207461519012659
dc.contributorMatta, Luciana Duarte Martins da
dc.contributor
dc.contributorhttp://lattes.cnpq.br/2752887804614967
dc.contributorSantos, Elizeu Antunes dos
dc.contributor
dc.contributorhttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4782221T9&dataRevisao=null
dc.creatorCruz, Ana Celly Bezerra
dc.date.accessioned2009-05-14
dc.date.accessioned2014-12-17T14:03:30Z
dc.date.accessioned2022-10-05T23:03:35Z
dc.date.available2009-05-14
dc.date.available2014-12-17T14:03:30Z
dc.date.available2022-10-05T23:03:35Z
dc.date.created2009-05-14
dc.date.created2014-12-17T14:03:30Z
dc.date.issued2008-10-20
dc.identifierCRUZ, 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.identifierhttps://repositorio.ufrn.br/jspui/handle/123456789/12544
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3945688
dc.description.abstractOne 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
dc.publisherUniversidade Federal do Rio Grande do Norte
dc.publisherBR
dc.publisherUFRN
dc.publisherPrograma de Pós-Graduação em Bioquímica
dc.publisherBioquímica; Biologia Molecular
dc.rightsAcesso Aberto
dc.subjectInibidor de tripsina
dc.subjectPiptadenia moniliformis
dc.subjectInsetos praga
dc.subjectBioinseticida
dc.subjectInibidor Kunitz
dc.subjectTrypsin inhibitor
dc.subjectPiptadenia moniliformis
dc.subjectInsect pests
dc.subjectBioinsecticide
dc.subjectKunitz inhibitor
dc.titlePurificação, caracterização e análise da atividade bioinseticida, de um inibidor de tripsina em sementes de catanduva (Piptadenia moniliformis)
dc.typemasterThesis


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