Lipase production by bacterial isolates from petroleum contaminated soil - DOI: 10.4025/actascitechnol.v32i1.7550

Detalhes bibliográficos
Autor(a) principal: Feitosa, Ingrid Cavalcanti
Data de Publicação: 2009
Outros Autores: Barbosa, José Murillo de Pinho, Orellana, Sara Cuadros, Lima, Álvaro Silva, Soares, Cleide Mara Faria
Tipo de documento: Artigo
Idioma: por
Título da fonte: Acta scientiarum. Technology (Online)
Texto Completo: http://www.periodicos.uem.br/ojs/index.php/ActaSciTechnol/article/view/7550
Resumo: Lipase production by bacterial isolates from petroleum contaminated soil. This paper aims to present alternatives to the production of lipolytic enzymes from microorganisms isolated from soil with a history of contact with oil from the region of Sergipe, by submerged fermentation using palm oil as inducer. The experiments were conduced in 250 mL Erlenmeyer flasks in a shaker (170 rpm), containing 125 mL (%, w v-1) of KH2PO4, MgSO4.7H2O, NaNO3, yeast extract, peptone and starch. The pH was 5.0 and 7.0; incubation temperature was 30 and 37°C, respectively; fermentation time was 24, 48, 72, 96h, 120 and 144h; and the inducer concentration was 3 and 4%, added after 72h of fermentation. The determination of lipolytic activity was examined at 37°C, in a shaker in thermostatic bath with rotation of 82 rpm, using gum arabic 7% (w v-1), olive oil and water. The reactions were conducted for 10 min with agitation and later stopped by the addition of an acetone:ethanol:water solution, where released fatty acids were titrated with a solution of KOH (0.04 N), using phenolphthalein as an indicator. The maximum activity was determined as 4369.75 U mL-1 pH 7.0 and a temperature of 37°C, with the percentage of the inducer oil palm to 4%.
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spelling Lipase production by bacterial isolates from petroleum contaminated soil - DOI: 10.4025/actascitechnol.v32i1.7550Produção de lipase por meio de microrganismos isolados de solos com histórico de contato com petróleo - DOI: 10.4025/actascitechnol.v32i1.7550submerged fermentationlipolytic activitiesinducerfermentação submersaatividade lipolíticaindutorLipase production by bacterial isolates from petroleum contaminated soil. This paper aims to present alternatives to the production of lipolytic enzymes from microorganisms isolated from soil with a history of contact with oil from the region of Sergipe, by submerged fermentation using palm oil as inducer. The experiments were conduced in 250 mL Erlenmeyer flasks in a shaker (170 rpm), containing 125 mL (%, w v-1) of KH2PO4, MgSO4.7H2O, NaNO3, yeast extract, peptone and starch. The pH was 5.0 and 7.0; incubation temperature was 30 and 37°C, respectively; fermentation time was 24, 48, 72, 96h, 120 and 144h; and the inducer concentration was 3 and 4%, added after 72h of fermentation. The determination of lipolytic activity was examined at 37°C, in a shaker in thermostatic bath with rotation of 82 rpm, using gum arabic 7% (w v-1), olive oil and water. The reactions were conducted for 10 min with agitation and later stopped by the addition of an acetone:ethanol:water solution, where released fatty acids were titrated with a solution of KOH (0.04 N), using phenolphthalein as an indicator. The maximum activity was determined as 4369.75 U mL-1 pH 7.0 and a temperature of 37°C, with the percentage of the inducer oil palm to 4%.O presente trabalho tem como objetivo apresentar alternativas para a produção de enzimas lipolíticas a partir de microrganismos isolados de solos com histórico de contato com petróleo da região de Sergipe, por fermentação submersa, utilizando o óleo de palma como indutor. Os experimentos foram conduzidos em frascos erlenmeyer de 250 mL, em agitador do tipo shaker (170 rpm), contendo 125 mL (%, w v-1) de KH2PO4, MgSO4.7H2O, NaNO3, extrato de levedura, peptona e amido. O pH foi de 5,0 e 7,0; a temperatura de incubação foi de 30 e 37ºC; o tempo de fermentação, de 24, 48, 72, 96, 120 e 144h; e a proporção de indutor foi de 3 e 4%, adicionado após 72h de fermentação. A determinação da atividade lipolítica foi analisada a 37ºC, num Shaker em banho termostático com agitasção, utilizando goma arábica 7% (p v-1); azeite de oliva e água. As reações foram conduzidas durante 10 min e posteriormente interrompida pela adição de uma solução acetanólica, e titulados com uma solução de KOH (0,04 N), utilizando a fenolftaleína como indicador. A máxima atividade determinada foi de 4369,75 U mL-1 a pH 7,0 e temperatura de 37ºC, com a porcentagem do indutor óleo de palma a 4%.Universidade Estadual De Maringá2009-11-13info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://www.periodicos.uem.br/ojs/index.php/ActaSciTechnol/article/view/755010.4025/actascitechnol.v32i1.7550Acta Scientiarum. Technology; Vol 32 No 1 (2010); 27-31Acta Scientiarum. Technology; v. 32 n. 1 (2010); 27-311806-25631807-8664reponame:Acta scientiarum. Technology (Online)instname:Universidade Estadual de Maringá (UEM)instacron:UEMporhttp://www.periodicos.uem.br/ojs/index.php/ActaSciTechnol/article/view/7550/7550Feitosa, Ingrid CavalcantiBarbosa, José Murillo de PinhoOrellana, Sara CuadrosLima, Álvaro SilvaSoares, Cleide Mara Fariainfo:eu-repo/semantics/openAccess2022-11-23T18:37:38Zoai:periodicos.uem.br/ojs:article/7550Revistahttp://periodicos.uem.br/ojs/index.php/ActaSciTechnolPUBhttp://www.periodicos.uem.br/ojs/index.php/ActaSciTechnol/oai||actatech@uem.br1807-86641806-2563opendoar:2022-11-23T18:37:38Acta scientiarum. Technology (Online) - Universidade Estadual de Maringá (UEM)false
dc.title.none.fl_str_mv Lipase production by bacterial isolates from petroleum contaminated soil - DOI: 10.4025/actascitechnol.v32i1.7550
Produção de lipase por meio de microrganismos isolados de solos com histórico de contato com petróleo - DOI: 10.4025/actascitechnol.v32i1.7550
title Lipase production by bacterial isolates from petroleum contaminated soil - DOI: 10.4025/actascitechnol.v32i1.7550
spellingShingle Lipase production by bacterial isolates from petroleum contaminated soil - DOI: 10.4025/actascitechnol.v32i1.7550
Feitosa, Ingrid Cavalcanti
submerged fermentation
lipolytic activities
inducer
fermentação submersa
atividade lipolítica
indutor
title_short Lipase production by bacterial isolates from petroleum contaminated soil - DOI: 10.4025/actascitechnol.v32i1.7550
title_full Lipase production by bacterial isolates from petroleum contaminated soil - DOI: 10.4025/actascitechnol.v32i1.7550
title_fullStr Lipase production by bacterial isolates from petroleum contaminated soil - DOI: 10.4025/actascitechnol.v32i1.7550
title_full_unstemmed Lipase production by bacterial isolates from petroleum contaminated soil - DOI: 10.4025/actascitechnol.v32i1.7550
title_sort Lipase production by bacterial isolates from petroleum contaminated soil - DOI: 10.4025/actascitechnol.v32i1.7550
author Feitosa, Ingrid Cavalcanti
author_facet Feitosa, Ingrid Cavalcanti
Barbosa, José Murillo de Pinho
Orellana, Sara Cuadros
Lima, Álvaro Silva
Soares, Cleide Mara Faria
author_role author
author2 Barbosa, José Murillo de Pinho
Orellana, Sara Cuadros
Lima, Álvaro Silva
Soares, Cleide Mara Faria
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Feitosa, Ingrid Cavalcanti
Barbosa, José Murillo de Pinho
Orellana, Sara Cuadros
Lima, Álvaro Silva
Soares, Cleide Mara Faria
dc.subject.por.fl_str_mv submerged fermentation
lipolytic activities
inducer
fermentação submersa
atividade lipolítica
indutor
topic submerged fermentation
lipolytic activities
inducer
fermentação submersa
atividade lipolítica
indutor
description Lipase production by bacterial isolates from petroleum contaminated soil. This paper aims to present alternatives to the production of lipolytic enzymes from microorganisms isolated from soil with a history of contact with oil from the region of Sergipe, by submerged fermentation using palm oil as inducer. The experiments were conduced in 250 mL Erlenmeyer flasks in a shaker (170 rpm), containing 125 mL (%, w v-1) of KH2PO4, MgSO4.7H2O, NaNO3, yeast extract, peptone and starch. The pH was 5.0 and 7.0; incubation temperature was 30 and 37°C, respectively; fermentation time was 24, 48, 72, 96h, 120 and 144h; and the inducer concentration was 3 and 4%, added after 72h of fermentation. The determination of lipolytic activity was examined at 37°C, in a shaker in thermostatic bath with rotation of 82 rpm, using gum arabic 7% (w v-1), olive oil and water. The reactions were conducted for 10 min with agitation and later stopped by the addition of an acetone:ethanol:water solution, where released fatty acids were titrated with a solution of KOH (0.04 N), using phenolphthalein as an indicator. The maximum activity was determined as 4369.75 U mL-1 pH 7.0 and a temperature of 37°C, with the percentage of the inducer oil palm to 4%.
publishDate 2009
dc.date.none.fl_str_mv 2009-11-13
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/ActaSciTechnol/article/view/7550
10.4025/actascitechnol.v32i1.7550
url http://www.periodicos.uem.br/ojs/index.php/ActaSciTechnol/article/view/7550
identifier_str_mv 10.4025/actascitechnol.v32i1.7550
dc.language.iso.fl_str_mv por
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dc.relation.none.fl_str_mv http://www.periodicos.uem.br/ojs/index.php/ActaSciTechnol/article/view/7550/7550
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. Technology; Vol 32 No 1 (2010); 27-31
Acta Scientiarum. Technology; v. 32 n. 1 (2010); 27-31
1806-2563
1807-8664
reponame:Acta scientiarum. Technology (Online)
instname:Universidade Estadual de Maringá (UEM)
instacron:UEM
instname_str Universidade Estadual de Maringá (UEM)
instacron_str UEM
institution UEM
reponame_str Acta scientiarum. Technology (Online)
collection Acta scientiarum. Technology (Online)
repository.name.fl_str_mv Acta scientiarum. Technology (Online) - Universidade Estadual de Maringá (UEM)
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