Optimization of fibrinolytic protease production from Bacillus subtilis I-2 using agro-residues

Detalhes bibliográficos
Autor(a) principal: Bajaj,Bijender Kumar
Data de Publicação: 2014
Outros Autores: Singh,Satbir, Khullar,Mowkshi, Singh,Kaurab, Bhardwaj,Shikha
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Archives of Biology and Technology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132014000500653
Resumo: The aim of this work was to study the production of fibrinolytic protease by Bacillus subtilis I-2 on agricultural residues. Molasses substantially enhanced (63%) protease production (652.32 U/mL) than control (398.64 U/mL). Soybean meal supported maximum protease production (797.28 U/mL), followed by malt extract (770.1 U/mL), cotton cake (761.04 U/mL), gelatin (742.92 U/mL) and beef extract (724.8 U/mL). Based on the Plackett-Burman designed experiments, incubation time, soybean meal, mustard cake and molasses were identified as the significant fermentation parameters. Ammonium sulfate precipitation and DEAE sephadex chromatography resulted 4.8-fold purification of protease. Zymography showed the presence of three iso-forms in the partially purified protease preparation, which was confirmed by the SDS-PAGE analysis (42, 48, 60 kDa). Protease exhibited maximum activity at 50oC and at pH 8.0. Significant stability was observed at 30-50oC and at pH 7.0-10.0. Mg2+, Zn2+, Co2+, Ca2+, Mn2+ and Cu2+,EGTA, EDTA and aprotinin severely decreased the enzyme activity.
id TECPAR-1_7f936fb7bea4f809945e74957495c569
oai_identifier_str oai:scielo:S1516-89132014000500653
network_acronym_str TECPAR-1
network_name_str Brazilian Archives of Biology and Technology
repository_id_str
spelling Optimization of fibrinolytic protease production from Bacillus subtilis I-2 using agro-residuesFibrinolytic ProteaseProductionAgricultural residuesBacillus subtilis I-2The aim of this work was to study the production of fibrinolytic protease by Bacillus subtilis I-2 on agricultural residues. Molasses substantially enhanced (63%) protease production (652.32 U/mL) than control (398.64 U/mL). Soybean meal supported maximum protease production (797.28 U/mL), followed by malt extract (770.1 U/mL), cotton cake (761.04 U/mL), gelatin (742.92 U/mL) and beef extract (724.8 U/mL). Based on the Plackett-Burman designed experiments, incubation time, soybean meal, mustard cake and molasses were identified as the significant fermentation parameters. Ammonium sulfate precipitation and DEAE sephadex chromatography resulted 4.8-fold purification of protease. Zymography showed the presence of three iso-forms in the partially purified protease preparation, which was confirmed by the SDS-PAGE analysis (42, 48, 60 kDa). Protease exhibited maximum activity at 50oC and at pH 8.0. Significant stability was observed at 30-50oC and at pH 7.0-10.0. Mg2+, Zn2+, Co2+, Ca2+, Mn2+ and Cu2+,EGTA, EDTA and aprotinin severely decreased the enzyme activity.Instituto de Tecnologia do Paraná - Tecpar2014-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132014000500653Brazilian Archives of Biology and Technology v.57 n.5 2014reponame:Brazilian Archives of Biology and Technologyinstname:Instituto de Tecnologia do Paraná (Tecpar)instacron:TECPAR10.1590/S1516-8913201402132info:eu-repo/semantics/openAccessBajaj,Bijender KumarSingh,SatbirKhullar,MowkshiSingh,KaurabBhardwaj,Shikhaeng2015-10-08T00:00:00Zoai:scielo:S1516-89132014000500653Revistahttps://www.scielo.br/j/babt/https://old.scielo.br/oai/scielo-oai.phpbabt@tecpar.br||babt@tecpar.br1678-43241516-8913opendoar:2015-10-08T00:00Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)false
dc.title.none.fl_str_mv Optimization of fibrinolytic protease production from Bacillus subtilis I-2 using agro-residues
title Optimization of fibrinolytic protease production from Bacillus subtilis I-2 using agro-residues
spellingShingle Optimization of fibrinolytic protease production from Bacillus subtilis I-2 using agro-residues
Bajaj,Bijender Kumar
Fibrinolytic Protease
Production
Agricultural residues
Bacillus subtilis I-2
title_short Optimization of fibrinolytic protease production from Bacillus subtilis I-2 using agro-residues
title_full Optimization of fibrinolytic protease production from Bacillus subtilis I-2 using agro-residues
title_fullStr Optimization of fibrinolytic protease production from Bacillus subtilis I-2 using agro-residues
title_full_unstemmed Optimization of fibrinolytic protease production from Bacillus subtilis I-2 using agro-residues
title_sort Optimization of fibrinolytic protease production from Bacillus subtilis I-2 using agro-residues
author Bajaj,Bijender Kumar
author_facet Bajaj,Bijender Kumar
Singh,Satbir
Khullar,Mowkshi
Singh,Kaurab
Bhardwaj,Shikha
author_role author
author2 Singh,Satbir
Khullar,Mowkshi
Singh,Kaurab
Bhardwaj,Shikha
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Bajaj,Bijender Kumar
Singh,Satbir
Khullar,Mowkshi
Singh,Kaurab
Bhardwaj,Shikha
dc.subject.por.fl_str_mv Fibrinolytic Protease
Production
Agricultural residues
Bacillus subtilis I-2
topic Fibrinolytic Protease
Production
Agricultural residues
Bacillus subtilis I-2
description The aim of this work was to study the production of fibrinolytic protease by Bacillus subtilis I-2 on agricultural residues. Molasses substantially enhanced (63%) protease production (652.32 U/mL) than control (398.64 U/mL). Soybean meal supported maximum protease production (797.28 U/mL), followed by malt extract (770.1 U/mL), cotton cake (761.04 U/mL), gelatin (742.92 U/mL) and beef extract (724.8 U/mL). Based on the Plackett-Burman designed experiments, incubation time, soybean meal, mustard cake and molasses were identified as the significant fermentation parameters. Ammonium sulfate precipitation and DEAE sephadex chromatography resulted 4.8-fold purification of protease. Zymography showed the presence of three iso-forms in the partially purified protease preparation, which was confirmed by the SDS-PAGE analysis (42, 48, 60 kDa). Protease exhibited maximum activity at 50oC and at pH 8.0. Significant stability was observed at 30-50oC and at pH 7.0-10.0. Mg2+, Zn2+, Co2+, Ca2+, Mn2+ and Cu2+,EGTA, EDTA and aprotinin severely decreased the enzyme activity.
publishDate 2014
dc.date.none.fl_str_mv 2014-10-01
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=S1516-89132014000500653
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132014000500653
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1516-8913201402132
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 Instituto de Tecnologia do Paraná - Tecpar
publisher.none.fl_str_mv Instituto de Tecnologia do Paraná - Tecpar
dc.source.none.fl_str_mv Brazilian Archives of Biology and Technology v.57 n.5 2014
reponame:Brazilian Archives of Biology and Technology
instname:Instituto de Tecnologia do Paraná (Tecpar)
instacron:TECPAR
instname_str Instituto de Tecnologia do Paraná (Tecpar)
instacron_str TECPAR
institution TECPAR
reponame_str Brazilian Archives of Biology and Technology
collection Brazilian Archives of Biology and Technology
repository.name.fl_str_mv Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)
repository.mail.fl_str_mv babt@tecpar.br||babt@tecpar.br
_version_ 1750318276444946432