Production and partial characterization of proteases from Mucor hiemalis URM3773
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Acta Scientiarum Biological Sciences |
Texto Completo: | http://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/21016 |
Resumo: | The current study evaluated the proteases production from 11 fungal species belonging to the genera Mucor, Rhizomucor and Absidia. The species were obtained from the Collection of Cultures URM at the Mycology Department-UFPE, Brazil. The best producing species was Mucor hiemalis URM 3773 (1.689 U mL-1). Plackett-Burman design methodology was employed to select the most effective parameter for protease production out of 11 medium components, including: concentration of filtrate soybean, glucose, incubation period, yeast extract, tryptone, pH, aeration, rotation, NH4Cl, MgSO4 and K2HPO4. Filtrated soybean concentration was the significant variable over the response variable, which was the specific protease activity. The crude enzyme extract showed optimal activity in pH 7.5 and at 50ºC. The enzyme was stable within a wide pH range from 5.8 to 8.0, in the phosphate buffer 0.1M and in stable temperature variation of 40-70ºC, for 180 minutes. The ions FeSO4, NaCl, MnCl2, MgCl2 and KCl stimulated the protease activity, whereas ZnCl2 ion inhibited the activity in 2.27%. Iodoacetic acid at 1mM was the proteases inhibitor that presented greater action.The results indicate that the studied enzyme have great potential for industrial application. |
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Production and partial characterization of proteases from Mucor hiemalis URM3773proteolytic activitysubstrate fermentation liquidPlackett-Burman designbiochemical characterizationMicrobiologia Industrial e de FermentaçãoThe current study evaluated the proteases production from 11 fungal species belonging to the genera Mucor, Rhizomucor and Absidia. The species were obtained from the Collection of Cultures URM at the Mycology Department-UFPE, Brazil. The best producing species was Mucor hiemalis URM 3773 (1.689 U mL-1). Plackett-Burman design methodology was employed to select the most effective parameter for protease production out of 11 medium components, including: concentration of filtrate soybean, glucose, incubation period, yeast extract, tryptone, pH, aeration, rotation, NH4Cl, MgSO4 and K2HPO4. Filtrated soybean concentration was the significant variable over the response variable, which was the specific protease activity. The crude enzyme extract showed optimal activity in pH 7.5 and at 50ºC. The enzyme was stable within a wide pH range from 5.8 to 8.0, in the phosphate buffer 0.1M and in stable temperature variation of 40-70ºC, for 180 minutes. The ions FeSO4, NaCl, MnCl2, MgCl2 and KCl stimulated the protease activity, whereas ZnCl2 ion inhibited the activity in 2.27%. Iodoacetic acid at 1mM was the proteases inhibitor that presented greater action.The results indicate that the studied enzyme have great potential for industrial application. Universidade Estadual De Maringá2015-03-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/2101610.4025/actascibiolsci.v37i1.21016Acta Scientiarum. Biological Sciences; Vol 37 No 1 (2015); 71-79Acta Scientiarum. Biological Sciences; v. 37 n. 1 (2015); 71-791807-863X1679-9283reponame:Acta Scientiarum Biological Sciencesinstname:Universidade Estadual de Maringá (UEM)instacron:UEMenghttp://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/21016/pdf_39Ribeiro, Roana Cecília dos SantosRibeiro, Thaís Rafaelle dos SantosSouza-Motta, Cristina Maria deMedeiros, Erika ValenteMoreira, Keila Aparecidainfo:eu-repo/semantics/openAccess2015-03-10T09:15:09Zoai:periodicos.uem.br/ojs:article/21016Revistahttp://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSciPUBhttp://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/oai||actabiol@uem.br1807-863X1679-9283opendoar:2015-03-10T09:15:09Acta Scientiarum Biological Sciences - Universidade Estadual de Maringá (UEM)false |
dc.title.none.fl_str_mv |
Production and partial characterization of proteases from Mucor hiemalis URM3773 |
title |
Production and partial characterization of proteases from Mucor hiemalis URM3773 |
spellingShingle |
Production and partial characterization of proteases from Mucor hiemalis URM3773 Ribeiro, Roana Cecília dos Santos proteolytic activity substrate fermentation liquid Plackett-Burman design biochemical characterization Microbiologia Industrial e de Fermentação |
title_short |
Production and partial characterization of proteases from Mucor hiemalis URM3773 |
title_full |
Production and partial characterization of proteases from Mucor hiemalis URM3773 |
title_fullStr |
Production and partial characterization of proteases from Mucor hiemalis URM3773 |
title_full_unstemmed |
Production and partial characterization of proteases from Mucor hiemalis URM3773 |
title_sort |
Production and partial characterization of proteases from Mucor hiemalis URM3773 |
author |
Ribeiro, Roana Cecília dos Santos |
author_facet |
Ribeiro, Roana Cecília dos Santos Ribeiro, Thaís Rafaelle dos Santos Souza-Motta, Cristina Maria de Medeiros, Erika Valente Moreira, Keila Aparecida |
author_role |
author |
author2 |
Ribeiro, Thaís Rafaelle dos Santos Souza-Motta, Cristina Maria de Medeiros, Erika Valente Moreira, Keila Aparecida |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Ribeiro, Roana Cecília dos Santos Ribeiro, Thaís Rafaelle dos Santos Souza-Motta, Cristina Maria de Medeiros, Erika Valente Moreira, Keila Aparecida |
dc.subject.por.fl_str_mv |
proteolytic activity substrate fermentation liquid Plackett-Burman design biochemical characterization Microbiologia Industrial e de Fermentação |
topic |
proteolytic activity substrate fermentation liquid Plackett-Burman design biochemical characterization Microbiologia Industrial e de Fermentação |
description |
The current study evaluated the proteases production from 11 fungal species belonging to the genera Mucor, Rhizomucor and Absidia. The species were obtained from the Collection of Cultures URM at the Mycology Department-UFPE, Brazil. The best producing species was Mucor hiemalis URM 3773 (1.689 U mL-1). Plackett-Burman design methodology was employed to select the most effective parameter for protease production out of 11 medium components, including: concentration of filtrate soybean, glucose, incubation period, yeast extract, tryptone, pH, aeration, rotation, NH4Cl, MgSO4 and K2HPO4. Filtrated soybean concentration was the significant variable over the response variable, which was the specific protease activity. The crude enzyme extract showed optimal activity in pH 7.5 and at 50ºC. The enzyme was stable within a wide pH range from 5.8 to 8.0, in the phosphate buffer 0.1M and in stable temperature variation of 40-70ºC, for 180 minutes. The ions FeSO4, NaCl, MnCl2, MgCl2 and KCl stimulated the protease activity, whereas ZnCl2 ion inhibited the activity in 2.27%. Iodoacetic acid at 1mM was the proteases inhibitor that presented greater action.The results indicate that the studied enzyme have great potential for industrial application. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-03-10 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/21016 10.4025/actascibiolsci.v37i1.21016 |
url |
http://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/21016 |
identifier_str_mv |
10.4025/actascibiolsci.v37i1.21016 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
http://www.periodicos.uem.br/ojs/index.php/ActaSciBiolSci/article/view/21016/pdf_39 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Estadual De Maringá |
publisher.none.fl_str_mv |
Universidade Estadual De Maringá |
dc.source.none.fl_str_mv |
Acta Scientiarum. Biological Sciences; Vol 37 No 1 (2015); 71-79 Acta Scientiarum. Biological Sciences; v. 37 n. 1 (2015); 71-79 1807-863X 1679-9283 reponame:Acta Scientiarum Biological Sciences instname:Universidade Estadual de Maringá (UEM) instacron:UEM |
instname_str |
Universidade Estadual de Maringá (UEM) |
instacron_str |
UEM |
institution |
UEM |
reponame_str |
Acta Scientiarum Biological Sciences |
collection |
Acta Scientiarum Biological Sciences |
repository.name.fl_str_mv |
Acta Scientiarum Biological Sciences - Universidade Estadual de Maringá (UEM) |
repository.mail.fl_str_mv |
||actabiol@uem.br |
_version_ |
1799317395961020416 |