Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom

Detalhes bibliográficos
Autor(a) principal: Lima, P. R. M. De
Data de Publicação: 2000
Outros Autores: Brochetto-braga, M. R. [UNESP], Chaud-netto, J.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S0104-79302000000100004
http://hdl.handle.net/11449/212339
Resumo: Some properties of a Africanized honeybee venom proteases were determined by enzymatic assays in solution, electrophoresis in SDS-PAGE, and gel filtration. Bee venom extracts were obtained by reservoir disruption, selective dialysis (cut off 12 kDa) to eliminate small components, such as the protease inhibitor present in the venom, and then fractionation of the dialyzed extract by gel filtration on a Sephadex G-100 column. The optimal conditions for the caseinolytic assays were pH 9.5, 2-hour digestion at 37 °C, and 1% casein concentration. The proteolytic activity was also determined by electrophoresis in SDS-PAGE with co-polymerized gelatin with three major bands of 66.0, 41.6, and 25.1 kDa. A principal serine-protease-like mechanism was revealed in the enriched fraction of proteolytic activity.
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spelling Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venomvenomafricanized beeApis melliferaproteolytic activitygel filtration chromatographySome properties of a Africanized honeybee venom proteases were determined by enzymatic assays in solution, electrophoresis in SDS-PAGE, and gel filtration. Bee venom extracts were obtained by reservoir disruption, selective dialysis (cut off 12 kDa) to eliminate small components, such as the protease inhibitor present in the venom, and then fractionation of the dialyzed extract by gel filtration on a Sephadex G-100 column. The optimal conditions for the caseinolytic assays were pH 9.5, 2-hour digestion at 37 °C, and 1% casein concentration. The proteolytic activity was also determined by electrophoresis in SDS-PAGE with co-polymerized gelatin with three major bands of 66.0, 41.6, and 25.1 kDa. A principal serine-protease-like mechanism was revealed in the enriched fraction of proteolytic activity.Universidade Estadual Paulista, Center for the Study of Venoms and Venomous Animals - CEVAPInstitute of Biosciences of Rio Claro, Department of BiologyUniversidade Estadual Paulista, Center of Study of Social InsectsUniversidade Estadual Paulista, Center for the Study of Venoms and Venomous Animals - CEVAPUniversidade Estadual Paulista, Center of Study of Social InsectsCentro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESPUniversidade Estadual Paulista (Unesp)Institute of Biosciences of Rio ClaroLima, P. R. M. DeBrochetto-braga, M. R. [UNESP]Chaud-netto, J.2021-07-14T10:38:23Z2021-07-14T10:38:23Z2000info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article64-76http://dx.doi.org/10.1590/S0104-79302000000100004Journal of Venomous Animals and Toxins. Botucatu, SP, Brazil: Centro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESP, v. 6, n. 1, p. 64-76, 2000.0104-79301678-4936http://hdl.handle.net/11449/21233910.1590/S0104-79302000000100004S0104-79302000000100004S0104-79302000000100004.pdfSciELOreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Venomous Animals and Toxinsinfo:eu-repo/semantics/openAccess2024-04-11T15:28:17Zoai:repositorio.unesp.br:11449/212339Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:38:21.935940Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom
title Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom
spellingShingle Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom
Lima, P. R. M. De
venom
africanized bee
Apis mellifera
proteolytic activity
gel filtration chromatography
title_short Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom
title_full Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom
title_fullStr Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom
title_full_unstemmed Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom
title_sort Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom
author Lima, P. R. M. De
author_facet Lima, P. R. M. De
Brochetto-braga, M. R. [UNESP]
Chaud-netto, J.
author_role author
author2 Brochetto-braga, M. R. [UNESP]
Chaud-netto, J.
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Institute of Biosciences of Rio Claro
dc.contributor.author.fl_str_mv Lima, P. R. M. De
Brochetto-braga, M. R. [UNESP]
Chaud-netto, J.
dc.subject.por.fl_str_mv venom
africanized bee
Apis mellifera
proteolytic activity
gel filtration chromatography
topic venom
africanized bee
Apis mellifera
proteolytic activity
gel filtration chromatography
description Some properties of a Africanized honeybee venom proteases were determined by enzymatic assays in solution, electrophoresis in SDS-PAGE, and gel filtration. Bee venom extracts were obtained by reservoir disruption, selective dialysis (cut off 12 kDa) to eliminate small components, such as the protease inhibitor present in the venom, and then fractionation of the dialyzed extract by gel filtration on a Sephadex G-100 column. The optimal conditions for the caseinolytic assays were pH 9.5, 2-hour digestion at 37 °C, and 1% casein concentration. The proteolytic activity was also determined by electrophoresis in SDS-PAGE with co-polymerized gelatin with three major bands of 66.0, 41.6, and 25.1 kDa. A principal serine-protease-like mechanism was revealed in the enriched fraction of proteolytic activity.
publishDate 2000
dc.date.none.fl_str_mv 2000
2021-07-14T10:38:23Z
2021-07-14T10:38:23Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0104-79302000000100004
Journal of Venomous Animals and Toxins. Botucatu, SP, Brazil: Centro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESP, v. 6, n. 1, p. 64-76, 2000.
0104-7930
1678-4936
http://hdl.handle.net/11449/212339
10.1590/S0104-79302000000100004
S0104-79302000000100004
S0104-79302000000100004.pdf
url http://dx.doi.org/10.1590/S0104-79302000000100004
http://hdl.handle.net/11449/212339
identifier_str_mv Journal of Venomous Animals and Toxins. Botucatu, SP, Brazil: Centro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESP, v. 6, n. 1, p. 64-76, 2000.
0104-7930
1678-4936
10.1590/S0104-79302000000100004
S0104-79302000000100004
S0104-79302000000100004.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Venomous Animals and Toxins
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 64-76
dc.publisher.none.fl_str_mv Centro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESP
publisher.none.fl_str_mv Centro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESP
dc.source.none.fl_str_mv SciELO
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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