Multiple forms of cotyledonary b-galactosidases from Vigna unguiculata quiescent seeds

Detalhes bibliográficos
Autor(a) principal: ENÉAS-FILHO,JOAQUIM
Data de Publicação: 2000
Outros Autores: SUDÉRIO,FABRÍCIO BONFIM, GOMES-FILHO,ENÉAS, PRISCO,JOSÉ TARQUÍNIO
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Botany
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-84042000000100008
Resumo: Cotyledonary b-galactosidases were isolated and partially purified from Pitiúba cowpea (Vigna unguiculata (L.) Walp.) quiescent seeds. The purification steps consisted of precipitation of the crude extract with ammonium sulphate in the range of 20-60% saturation, acid precipitation, DEAE-Sephadex ion-exchange chromatography and Lactosyl-Sepharose affinity chromatography. This purification process gave rise to three b-galactosidases-rich fractions: b-gal I, b-gal II and b-gal III, which were purified about 5, 509, and 62 fold, respectively. They reached maximal enzyme activity at different pH ranges: 3.5-4.5 for b-gal I, 3.0-3.5 for b-gal II, and 3.0-4.0 for b-gal III. Their maximal activities were reached when the temperature of the assay medium was 60° C, and preincubation of the enzymes at different temperatures has shown that they were heat-stable up to 50° C. There were no significant differences among the partially purified enzymes as far as their response to the different effectors tested, except for Mn2+ and EDTA, which affected differently b-gal I, b-gal II, and b-gal III. They were slightly affected by Mg2+, Ca2+, Zn2+, Co2+, tartarate, molybdate, glucose, and lactose, strongly inhibited by Cu2+ and galactose, and inactivated by Hg2+. These chemical and physical properties are similar to the ones found for other plant b-galactosidases. Although through this process of purification three isoforms of this enzyme were obtained, isoelectric focusing in polyacrylamide slab gel of these enzyme-proteins suggest that cotyledons of Pitiúba cowpea quiescent seeds possess four isoforms of b-galactosidases.
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spelling Multiple forms of cotyledonary b-galactosidases from Vigna unguiculata quiescent seedsCotyledonscowpeaenzyme purificationquiescent seedsCotyledonary b-galactosidases were isolated and partially purified from Pitiúba cowpea (Vigna unguiculata (L.) Walp.) quiescent seeds. The purification steps consisted of precipitation of the crude extract with ammonium sulphate in the range of 20-60% saturation, acid precipitation, DEAE-Sephadex ion-exchange chromatography and Lactosyl-Sepharose affinity chromatography. This purification process gave rise to three b-galactosidases-rich fractions: b-gal I, b-gal II and b-gal III, which were purified about 5, 509, and 62 fold, respectively. They reached maximal enzyme activity at different pH ranges: 3.5-4.5 for b-gal I, 3.0-3.5 for b-gal II, and 3.0-4.0 for b-gal III. Their maximal activities were reached when the temperature of the assay medium was 60° C, and preincubation of the enzymes at different temperatures has shown that they were heat-stable up to 50° C. There were no significant differences among the partially purified enzymes as far as their response to the different effectors tested, except for Mn2+ and EDTA, which affected differently b-gal I, b-gal II, and b-gal III. They were slightly affected by Mg2+, Ca2+, Zn2+, Co2+, tartarate, molybdate, glucose, and lactose, strongly inhibited by Cu2+ and galactose, and inactivated by Hg2+. These chemical and physical properties are similar to the ones found for other plant b-galactosidases. Although through this process of purification three isoforms of this enzyme were obtained, isoelectric focusing in polyacrylamide slab gel of these enzyme-proteins suggest that cotyledons of Pitiúba cowpea quiescent seeds possess four isoforms of b-galactosidases.Sociedade Botânica de São Paulo2000-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-84042000000100008Brazilian Journal of Botany v.23 n.1 2000reponame:Brazilian Journal of Botanyinstname:Sociedade Botânica de São Paulo (SBSP)instacron:SBSP10.1590/S0100-84042000000100008info:eu-repo/semantics/openAccessENÉAS-FILHO,JOAQUIMSUDÉRIO,FABRÍCIO BONFIMGOMES-FILHO,ENÉASPRISCO,JOSÉ TARQUÍNIOeng2000-05-11T00:00:00Zoai:scielo:S0100-84042000000100008Revistahttps://www.scielo.br/j/rbb/ONGhttps://old.scielo.br/oai/scielo-oai.phpbrazbot@gmail.com||brazbot@gmail.com1806-99590100-8404opendoar:2000-05-11T00:00Brazilian Journal of Botany - Sociedade Botânica de São Paulo (SBSP)false
dc.title.none.fl_str_mv Multiple forms of cotyledonary b-galactosidases from Vigna unguiculata quiescent seeds
title Multiple forms of cotyledonary b-galactosidases from Vigna unguiculata quiescent seeds
spellingShingle Multiple forms of cotyledonary b-galactosidases from Vigna unguiculata quiescent seeds
ENÉAS-FILHO,JOAQUIM
Cotyledons
cowpea
enzyme purification
quiescent seeds
title_short Multiple forms of cotyledonary b-galactosidases from Vigna unguiculata quiescent seeds
title_full Multiple forms of cotyledonary b-galactosidases from Vigna unguiculata quiescent seeds
title_fullStr Multiple forms of cotyledonary b-galactosidases from Vigna unguiculata quiescent seeds
title_full_unstemmed Multiple forms of cotyledonary b-galactosidases from Vigna unguiculata quiescent seeds
title_sort Multiple forms of cotyledonary b-galactosidases from Vigna unguiculata quiescent seeds
author ENÉAS-FILHO,JOAQUIM
author_facet ENÉAS-FILHO,JOAQUIM
SUDÉRIO,FABRÍCIO BONFIM
GOMES-FILHO,ENÉAS
PRISCO,JOSÉ TARQUÍNIO
author_role author
author2 SUDÉRIO,FABRÍCIO BONFIM
GOMES-FILHO,ENÉAS
PRISCO,JOSÉ TARQUÍNIO
author2_role author
author
author
dc.contributor.author.fl_str_mv ENÉAS-FILHO,JOAQUIM
SUDÉRIO,FABRÍCIO BONFIM
GOMES-FILHO,ENÉAS
PRISCO,JOSÉ TARQUÍNIO
dc.subject.por.fl_str_mv Cotyledons
cowpea
enzyme purification
quiescent seeds
topic Cotyledons
cowpea
enzyme purification
quiescent seeds
description Cotyledonary b-galactosidases were isolated and partially purified from Pitiúba cowpea (Vigna unguiculata (L.) Walp.) quiescent seeds. The purification steps consisted of precipitation of the crude extract with ammonium sulphate in the range of 20-60% saturation, acid precipitation, DEAE-Sephadex ion-exchange chromatography and Lactosyl-Sepharose affinity chromatography. This purification process gave rise to three b-galactosidases-rich fractions: b-gal I, b-gal II and b-gal III, which were purified about 5, 509, and 62 fold, respectively. They reached maximal enzyme activity at different pH ranges: 3.5-4.5 for b-gal I, 3.0-3.5 for b-gal II, and 3.0-4.0 for b-gal III. Their maximal activities were reached when the temperature of the assay medium was 60° C, and preincubation of the enzymes at different temperatures has shown that they were heat-stable up to 50° C. There were no significant differences among the partially purified enzymes as far as their response to the different effectors tested, except for Mn2+ and EDTA, which affected differently b-gal I, b-gal II, and b-gal III. They were slightly affected by Mg2+, Ca2+, Zn2+, Co2+, tartarate, molybdate, glucose, and lactose, strongly inhibited by Cu2+ and galactose, and inactivated by Hg2+. These chemical and physical properties are similar to the ones found for other plant b-galactosidases. Although through this process of purification three isoforms of this enzyme were obtained, isoelectric focusing in polyacrylamide slab gel of these enzyme-proteins suggest that cotyledons of Pitiúba cowpea quiescent seeds possess four isoforms of b-galactosidases.
publishDate 2000
dc.date.none.fl_str_mv 2000-03-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-84042000000100008
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-84042000000100008
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0100-84042000000100008
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Botânica de São Paulo
publisher.none.fl_str_mv Sociedade Botânica de São Paulo
dc.source.none.fl_str_mv Brazilian Journal of Botany v.23 n.1 2000
reponame:Brazilian Journal of Botany
instname:Sociedade Botânica de São Paulo (SBSP)
instacron:SBSP
instname_str Sociedade Botânica de São Paulo (SBSP)
instacron_str SBSP
institution SBSP
reponame_str Brazilian Journal of Botany
collection Brazilian Journal of Botany
repository.name.fl_str_mv Brazilian Journal of Botany - Sociedade Botânica de São Paulo (SBSP)
repository.mail.fl_str_mv brazbot@gmail.com||brazbot@gmail.com
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