Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom
Autor(a) principal: | |
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Data de Publicação: | 2000 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
DOI: | 10.1590/S0104-79302000000100004 |
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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Repositório Institucional da UNESP |
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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 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 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 Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom |
title_full_unstemmed |
Proteolytic activity of africanized honeybee (Apis mellifera: hymenoptera, apidae) venom 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 Lima, P. R. M. De Brochetto-braga, M. R. [UNESP] Chaud-netto, J. 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 |
|
_version_ |
1822231395110486016 |
dc.identifier.doi.none.fl_str_mv |
10.1590/S0104-79302000000100004 |