Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes

Detalhes bibliográficos
Autor(a) principal: Silva, Diogo P.
Data de Publicação: 2007
Outros Autores: Casado-Filho, Erivaldo L., Corrêa, Andréa S. R., Farias, Luciana Ramalho, Bloch Júnior, Carlos, Grossi-de-Sá, Maria Fátima, Mendes, Paulo A. M., Quirino, Betânia F., Noronha, Eliana Ferreira, Franco, Octávio Luiz
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UCB
Texto Completo: http://twingo.ucb.br:8080/jspui/handle/10869/514
https://repositorio.ucb.br:9443/jspui/handle/123456789/7728
Resumo: Cowpea seeds (Vigna ungiculata) are widely cultivated by poor farmers in Latin America and Africa and are often severely damaged by the cowpea weevil Callosobruchus maculatus. A proteinaceous inhibitor of cowpea weevil digestive enzymes, PpAI, was purified from white sucupira seeds (Pterodon pubescens) and biochemically characterized in this study. Proteins were extracted from seeds and precipitated with ammonium sulfate at 100% saturation. This fraction was applied onto a Redsepharose CL-6B column, and the retained peak showed 70% inhibitory activity toward larval C. maculatus digestive R-amylases. The retained peak was then purified using an analytical reversedphase HPLC column. Purified PpAI showed 65% inhibitory activity against larval C. maculatus enzymes. Enzymatic assays also showed that the purified P. pubescens inhibitor was unable to reduce the activity of mammalian R-amylases, suggesting specificity toward insect enzymes. Moreover, artificial seeds containing PpAI were able to reduce larval weight by 36% and cause 55% mortality. Mass spectrometry and SDS-PAGE analyses indicated that PpAI showed a molecular mass of approximately 5.0 kDa. This R-amylase inhibitor, coming from a native Cerrado plant, could be used to construct a genetically engineered cowpea with enhanced resistance against weevil pests.
id UCB-2_eeeea0127d9e8014fbe6366943ff7ddd
oai_identifier_str oai:200.214.135.189:123456789/7728
network_acronym_str UCB-2
network_name_str Repositório Institucional da UCB
spelling Silva, Diogo P.Casado-Filho, Erivaldo L.Corrêa, Andréa S. R.Farias, Luciana RamalhoBloch Júnior, CarlosGrossi-de-Sá, Maria FátimaMendes, Paulo A. M.Quirino, Betânia F.Noronha, Eliana FerreiraFranco, Octávio Luiz2016-10-10T03:52:30Z2016-10-10T03:52:30Z2007SILVA, Diogo P. et al. Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes. Journal of Agricultural and Food Chemistry, v. 55, p. 4382-4387, 2007.218561http://twingo.ucb.br:8080/jspui/handle/10869/514https://repositorio.ucb.br:9443/jspui/handle/123456789/7728Cowpea seeds (Vigna ungiculata) are widely cultivated by poor farmers in Latin America and Africa and are often severely damaged by the cowpea weevil Callosobruchus maculatus. A proteinaceous inhibitor of cowpea weevil digestive enzymes, PpAI, was purified from white sucupira seeds (Pterodon pubescens) and biochemically characterized in this study. Proteins were extracted from seeds and precipitated with ammonium sulfate at 100% saturation. This fraction was applied onto a Redsepharose CL-6B column, and the retained peak showed 70% inhibitory activity toward larval C. maculatus digestive R-amylases. The retained peak was then purified using an analytical reversedphase HPLC column. Purified PpAI showed 65% inhibitory activity against larval C. maculatus enzymes. Enzymatic assays also showed that the purified P. pubescens inhibitor was unable to reduce the activity of mammalian R-amylases, suggesting specificity toward insect enzymes. Moreover, artificial seeds containing PpAI were able to reduce larval weight by 36% and cause 55% mortality. Mass spectrometry and SDS-PAGE analyses indicated that PpAI showed a molecular mass of approximately 5.0 kDa. This R-amylase inhibitor, coming from a native Cerrado plant, could be used to construct a genetically engineered cowpea with enhanced resistance against weevil pests.Made available in DSpace on 2016-10-10T03:52:30Z (GMT). No. of bitstreams: 5 Identification of an Amylase Inhibitor from Pterodon.PDF: 152819 bytes, checksum: fb33a80bd863f26fe3af5329bb410d01 (MD5) license_url: 52 bytes, checksum: 2f32edb9c19a57e928372a33fd08dba5 (MD5) license_text: 24372 bytes, checksum: 94b0a37ff5ec51de8c55507bff4a7ff9 (MD5) license_rdf: 24623 bytes, checksum: 378d22d8fe50e084ee2f354be78cbe62 (MD5) license.txt: 1887 bytes, checksum: 445d1980f282ec865917de35a4c622f6 (MD5) Previous issue date: 2007SimPublicadoTextoRestrito UCBinfo:eu-repo/semantics/openAccessCallosobruchus maculatusPterodon pubescensPlant defenseA-Amylase InhibitorIdentification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleJournal of Agricultural and Food Chemistryengreponame:Repositório Institucional da UCBinstname:Universidade Católica de Brasília (UCB)instacron:UCBORIGINALIdentification of an Amylase Inhibitor from Pterodon.PDFapplication/pdf152819https://200.214.135.178:9443/jspui/bitstream/123456789/7728/1/Identification%20of%20an%20Amylase%20Inhibitor%20from%20Pterodon.PDFfb33a80bd863f26fe3af5329bb410d01MD51CC-LICENSElicense_urlapplication/octet-stream52https://200.214.135.178:9443/jspui/bitstream/123456789/7728/2/license_url2f32edb9c19a57e928372a33fd08dba5MD52license_textapplication/octet-stream24372https://200.214.135.178:9443/jspui/bitstream/123456789/7728/3/license_text94b0a37ff5ec51de8c55507bff4a7ff9MD53license_rdfapplication/octet-stream24623https://200.214.135.178:9443/jspui/bitstream/123456789/7728/4/license_rdf378d22d8fe50e084ee2f354be78cbe62MD54LICENSElicense.txttext/plain1887https://200.214.135.178:9443/jspui/bitstream/123456789/7728/5/license.txt445d1980f282ec865917de35a4c622f6MD55TEXTIdentification of an Amylase Inhibitor from Pterodon.PDF.txtIdentification of an Amylase Inhibitor from Pterodon.PDF.txtExtracted texttext/plain31894https://200.214.135.178:9443/jspui/bitstream/123456789/7728/6/Identification%20of%20an%20Amylase%20Inhibitor%20from%20Pterodon.PDF.txt3389e2bc23002e74db5e608854d90f39MD56123456789/77282017-01-17 15:10:26.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ório de Publicaçõeshttps://repositorio.ucb.br:9443/jspui/
dc.title.pt_BR.fl_str_mv Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes
title Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes
spellingShingle Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes
Silva, Diogo P.
Callosobruchus maculatus
Pterodon pubescens
Plant defense
A-Amylase Inhibitor
title_short Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes
title_full Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes
title_fullStr Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes
title_full_unstemmed Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes
title_sort Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes
author Silva, Diogo P.
author_facet Silva, Diogo P.
Casado-Filho, Erivaldo L.
Corrêa, Andréa S. R.
Farias, Luciana Ramalho
Bloch Júnior, Carlos
Grossi-de-Sá, Maria Fátima
Mendes, Paulo A. M.
Quirino, Betânia F.
Noronha, Eliana Ferreira
Franco, Octávio Luiz
author_role author
author2 Casado-Filho, Erivaldo L.
Corrêa, Andréa S. R.
Farias, Luciana Ramalho
Bloch Júnior, Carlos
Grossi-de-Sá, Maria Fátima
Mendes, Paulo A. M.
Quirino, Betânia F.
Noronha, Eliana Ferreira
Franco, Octávio Luiz
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Silva, Diogo P.
Casado-Filho, Erivaldo L.
Corrêa, Andréa S. R.
Farias, Luciana Ramalho
Bloch Júnior, Carlos
Grossi-de-Sá, Maria Fátima
Mendes, Paulo A. M.
Quirino, Betânia F.
Noronha, Eliana Ferreira
Franco, Octávio Luiz
dc.subject.por.fl_str_mv Callosobruchus maculatus
Pterodon pubescens
Plant defense
A-Amylase Inhibitor
topic Callosobruchus maculatus
Pterodon pubescens
Plant defense
A-Amylase Inhibitor
dc.description.abstract.por.fl_txt_mv Cowpea seeds (Vigna ungiculata) are widely cultivated by poor farmers in Latin America and Africa and are often severely damaged by the cowpea weevil Callosobruchus maculatus. A proteinaceous inhibitor of cowpea weevil digestive enzymes, PpAI, was purified from white sucupira seeds (Pterodon pubescens) and biochemically characterized in this study. Proteins were extracted from seeds and precipitated with ammonium sulfate at 100% saturation. This fraction was applied onto a Redsepharose CL-6B column, and the retained peak showed 70% inhibitory activity toward larval C. maculatus digestive R-amylases. The retained peak was then purified using an analytical reversedphase HPLC column. Purified PpAI showed 65% inhibitory activity against larval C. maculatus enzymes. Enzymatic assays also showed that the purified P. pubescens inhibitor was unable to reduce the activity of mammalian R-amylases, suggesting specificity toward insect enzymes. Moreover, artificial seeds containing PpAI were able to reduce larval weight by 36% and cause 55% mortality. Mass spectrometry and SDS-PAGE analyses indicated that PpAI showed a molecular mass of approximately 5.0 kDa. This R-amylase inhibitor, coming from a native Cerrado plant, could be used to construct a genetically engineered cowpea with enhanced resistance against weevil pests.
dc.description.version.pt_BR.fl_txt_mv Sim
dc.description.status.pt_BR.fl_txt_mv Publicado
description Cowpea seeds (Vigna ungiculata) are widely cultivated by poor farmers in Latin America and Africa and are often severely damaged by the cowpea weevil Callosobruchus maculatus. A proteinaceous inhibitor of cowpea weevil digestive enzymes, PpAI, was purified from white sucupira seeds (Pterodon pubescens) and biochemically characterized in this study. Proteins were extracted from seeds and precipitated with ammonium sulfate at 100% saturation. This fraction was applied onto a Redsepharose CL-6B column, and the retained peak showed 70% inhibitory activity toward larval C. maculatus digestive R-amylases. The retained peak was then purified using an analytical reversedphase HPLC column. Purified PpAI showed 65% inhibitory activity against larval C. maculatus enzymes. Enzymatic assays also showed that the purified P. pubescens inhibitor was unable to reduce the activity of mammalian R-amylases, suggesting specificity toward insect enzymes. Moreover, artificial seeds containing PpAI were able to reduce larval weight by 36% and cause 55% mortality. Mass spectrometry and SDS-PAGE analyses indicated that PpAI showed a molecular mass of approximately 5.0 kDa. This R-amylase inhibitor, coming from a native Cerrado plant, could be used to construct a genetically engineered cowpea with enhanced resistance against weevil pests.
publishDate 2007
dc.date.issued.fl_str_mv 2007
dc.date.accessioned.fl_str_mv 2016-10-10T03:52:30Z
dc.date.available.fl_str_mv 2016-10-10T03:52:30Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
status_str publishedVersion
format article
dc.identifier.citation.fl_str_mv SILVA, Diogo P. et al. Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes. Journal of Agricultural and Food Chemistry, v. 55, p. 4382-4387, 2007.
dc.identifier.uri.fl_str_mv http://twingo.ucb.br:8080/jspui/handle/10869/514
https://repositorio.ucb.br:9443/jspui/handle/123456789/7728
dc.identifier.issn.none.fl_str_mv 218561
identifier_str_mv SILVA, Diogo P. et al. Identification of an a-Amylase inhibitor from pterodon pubescens with ability to inhibit cowpea weevil digestive enzymes. Journal of Agricultural and Food Chemistry, v. 55, p. 4382-4387, 2007.
218561
url http://twingo.ucb.br:8080/jspui/handle/10869/514
https://repositorio.ucb.br:9443/jspui/handle/123456789/7728
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv Restrito UCB
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Restrito UCB
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv Texto
dc.source.none.fl_str_mv reponame:Repositório Institucional da UCB
instname:Universidade Católica de Brasília (UCB)
instacron:UCB
instname_str Universidade Católica de Brasília (UCB)
instacron_str UCB
institution UCB
reponame_str Repositório Institucional da UCB
collection Repositório Institucional da UCB
bitstream.url.fl_str_mv https://200.214.135.178:9443/jspui/bitstream/123456789/7728/1/Identification%20of%20an%20Amylase%20Inhibitor%20from%20Pterodon.PDF
https://200.214.135.178:9443/jspui/bitstream/123456789/7728/2/license_url
https://200.214.135.178:9443/jspui/bitstream/123456789/7728/3/license_text
https://200.214.135.178:9443/jspui/bitstream/123456789/7728/4/license_rdf
https://200.214.135.178:9443/jspui/bitstream/123456789/7728/5/license.txt
https://200.214.135.178:9443/jspui/bitstream/123456789/7728/6/Identification%20of%20an%20Amylase%20Inhibitor%20from%20Pterodon.PDF.txt
bitstream.checksum.fl_str_mv fb33a80bd863f26fe3af5329bb410d01
2f32edb9c19a57e928372a33fd08dba5
94b0a37ff5ec51de8c55507bff4a7ff9
378d22d8fe50e084ee2f354be78cbe62
445d1980f282ec865917de35a4c622f6
3389e2bc23002e74db5e608854d90f39
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
MD5
MD5
MD5
repository.name.fl_str_mv
repository.mail.fl_str_mv
_version_ 1724829830840582144