Using Pichia pastoris to produce recombinant glycerol kinase

Detalhes bibliográficos
Autor(a) principal: Terrazas, Werner Damião Morhy
Data de Publicação: 2014
Outros Autores: Aizemberg, Raquel [UNESP], Gattas, Edwil Aparecida de Lucca [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://serv-bib.fcfar.unesp.br/seer/index.php/Cien_Farm/article/view/3143
http://hdl.handle.net/11449/133661
Resumo: The methylotrophic yeast Pichia pastoris has been developed into an efficient expression system for the production of recombinant protein under the tight control of the methanol-induced alcohol oxidase promoter (pAOX1). In this study, a 2.5-liter culture system was developed for the growth of a P. pastoris strain bearing the GUT1 gene from Saccharomyces cerevisiae for the expression of recombinant glycerol kinase (GK). The best culture conditions to produce high levels of secreted GK were investigated by growing the recombinant strain of P. pastoris in shake flasks and a fermenter. Cell growth and enzyme production were found to be optimal after two days of growth. Enzyme production was affected by the nitrogen source, Difco peptone being the most appropriate for this purpose. Three different rates of air flow (1 to 3 L/min) were tested to observe their effect on cell growth and the secretion of GK into a medium containing 1% methanol as the sole carbon source. Increasing the rate of air bubbling in the culture medium enhanced both cell growth and GK activity, reaching a dry biomass of 7.84 mg/mL, cell viability of 98.4% and a maximal GK activity of 1.57 U/ mL, at a flow rate of 2.0 L/minute, at 30° C and pH 6.0. Moreover, the enzyme activity in the P. pastoris culture medium was 2.3 times higher under these conditions than in the shake-flask culture, demonstrating the significant influence of aeration on biomass production and GK activity secreted by P. pastoris.
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spelling Using Pichia pastoris to produce recombinant glycerol kinaseProdução de glycerol quinase recombinante utilizando o sistema Pichia pastorisPichia pastorisGlycerol kinaseOxygenBiomassPichia pastorisGlicerol quinaseOxigênioBiomassaThe methylotrophic yeast Pichia pastoris has been developed into an efficient expression system for the production of recombinant protein under the tight control of the methanol-induced alcohol oxidase promoter (pAOX1). In this study, a 2.5-liter culture system was developed for the growth of a P. pastoris strain bearing the GUT1 gene from Saccharomyces cerevisiae for the expression of recombinant glycerol kinase (GK). The best culture conditions to produce high levels of secreted GK were investigated by growing the recombinant strain of P. pastoris in shake flasks and a fermenter. Cell growth and enzyme production were found to be optimal after two days of growth. Enzyme production was affected by the nitrogen source, Difco peptone being the most appropriate for this purpose. Three different rates of air flow (1 to 3 L/min) were tested to observe their effect on cell growth and the secretion of GK into a medium containing 1% methanol as the sole carbon source. Increasing the rate of air bubbling in the culture medium enhanced both cell growth and GK activity, reaching a dry biomass of 7.84 mg/mL, cell viability of 98.4% and a maximal GK activity of 1.57 U/ mL, at a flow rate of 2.0 L/minute, at 30° C and pH 6.0. Moreover, the enzyme activity in the P. pastoris culture medium was 2.3 times higher under these conditions than in the shake-flask culture, demonstrating the significant influence of aeration on biomass production and GK activity secreted by P. pastoris.A levedura metilotrófica Pichia pastoris possui um sistema de expressão eficiente para a produção de proteínas recombinantes. A indução da produção da proteína de interesse é feita com metanol, que é capaz de ativar a transcrição do gene de interesse clonado sob controle do promotor do gene AOX1. Um meio de cultura de 2.5 litros foi elaborado para o crescimento da cepa Pichia pastoris construída com o gene GUT1 de Saccharomyces cerevisiae para expressar a enzima recombinante glicerol quinase (GK). As condições ideais de cultura, para alcançar altos níveis de expressão de GK foram investigados em crescimentos realizados em frascos e fermentador. Crescimento celular e produção de enzima atingiram valores ótimos em dois dias de cultura. A produção enzimática foi afetada pela fonte de nitrogênio no meio. Peptona da marca Difco foi a fonte de nitrogênio mais adequada para a expressão desta enzima. Três diferentes concentrações (1-3 L / min) de fluxo de ar foram analisados em ensaios de crescimento celular e secreção da GK, no meio contendo 1 % de metanol como única fonte de carbono. O aumento do fluxo do ar no meio de cultura produziu melhores resultados para o crescimento celular e atividade da GK, atingindo 7,84 mg / mL de biomassa seca e 98,4% de viabilidade. A máxima atividade de GK foi de 1,57 U / mL, com a concentração de fluxo de ar de 2,0 L / minuto a 30 ° C e pH 6.0. O aumento da atividade enzimática foi 2,3 vezes maior no meio de cultura da Pichia pastoris nestas condições, revelando a influência deste parâmetro na produção de biomassa e atividade da GK.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Universidade do Estado do Pará, Departamento de Tecnologia de Alimentos, Centro de Ciências Naturais e TecnologicasUniversidade Estadual Paulista, Departamento de Alimentos e Nutrição, Faculdade de Ciências Farmacêuticas de AraraquaraUniversidade Estadual Paulista (Unesp)Universidade do Estado do Pará (UEPA)Terrazas, Werner Damião MorhyAizemberg, Raquel [UNESP]Gattas, Edwil Aparecida de Lucca [UNESP]2016-01-28T16:56:04Z2016-01-28T16:56:04Z2014info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article277-282application/pdfhttp://serv-bib.fcfar.unesp.br/seer/index.php/Cien_Farm/article/view/3143Revista de Ciências Farmacêuticas Básica e Aplicada, v. 35, n. 2, p. 277-282, 2014.1808-4532http://hdl.handle.net/11449/133661ISSN1808-4532-2014-35-02-277-282.pdf72109866794427514006598610021833Currículo Lattesreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengRevista de Ciências Farmacêuticas Básica e Aplicada0,131info:eu-repo/semantics/openAccess2024-06-21T12:46:50Zoai:repositorio.unesp.br:11449/133661Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-06-21T12:46:50Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Using Pichia pastoris to produce recombinant glycerol kinase
Produção de glycerol quinase recombinante utilizando o sistema Pichia pastoris
title Using Pichia pastoris to produce recombinant glycerol kinase
spellingShingle Using Pichia pastoris to produce recombinant glycerol kinase
Terrazas, Werner Damião Morhy
Pichia pastoris
Glycerol kinase
Oxygen
Biomass
Pichia pastoris
Glicerol quinase
Oxigênio
Biomassa
title_short Using Pichia pastoris to produce recombinant glycerol kinase
title_full Using Pichia pastoris to produce recombinant glycerol kinase
title_fullStr Using Pichia pastoris to produce recombinant glycerol kinase
title_full_unstemmed Using Pichia pastoris to produce recombinant glycerol kinase
title_sort Using Pichia pastoris to produce recombinant glycerol kinase
author Terrazas, Werner Damião Morhy
author_facet Terrazas, Werner Damião Morhy
Aizemberg, Raquel [UNESP]
Gattas, Edwil Aparecida de Lucca [UNESP]
author_role author
author2 Aizemberg, Raquel [UNESP]
Gattas, Edwil Aparecida de Lucca [UNESP]
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade do Estado do Pará (UEPA)
dc.contributor.author.fl_str_mv Terrazas, Werner Damião Morhy
Aizemberg, Raquel [UNESP]
Gattas, Edwil Aparecida de Lucca [UNESP]
dc.subject.por.fl_str_mv Pichia pastoris
Glycerol kinase
Oxygen
Biomass
Pichia pastoris
Glicerol quinase
Oxigênio
Biomassa
topic Pichia pastoris
Glycerol kinase
Oxygen
Biomass
Pichia pastoris
Glicerol quinase
Oxigênio
Biomassa
description The methylotrophic yeast Pichia pastoris has been developed into an efficient expression system for the production of recombinant protein under the tight control of the methanol-induced alcohol oxidase promoter (pAOX1). In this study, a 2.5-liter culture system was developed for the growth of a P. pastoris strain bearing the GUT1 gene from Saccharomyces cerevisiae for the expression of recombinant glycerol kinase (GK). The best culture conditions to produce high levels of secreted GK were investigated by growing the recombinant strain of P. pastoris in shake flasks and a fermenter. Cell growth and enzyme production were found to be optimal after two days of growth. Enzyme production was affected by the nitrogen source, Difco peptone being the most appropriate for this purpose. Three different rates of air flow (1 to 3 L/min) were tested to observe their effect on cell growth and the secretion of GK into a medium containing 1% methanol as the sole carbon source. Increasing the rate of air bubbling in the culture medium enhanced both cell growth and GK activity, reaching a dry biomass of 7.84 mg/mL, cell viability of 98.4% and a maximal GK activity of 1.57 U/ mL, at a flow rate of 2.0 L/minute, at 30° C and pH 6.0. Moreover, the enzyme activity in the P. pastoris culture medium was 2.3 times higher under these conditions than in the shake-flask culture, demonstrating the significant influence of aeration on biomass production and GK activity secreted by P. pastoris.
publishDate 2014
dc.date.none.fl_str_mv 2014
2016-01-28T16:56:04Z
2016-01-28T16:56:04Z
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://serv-bib.fcfar.unesp.br/seer/index.php/Cien_Farm/article/view/3143
Revista de Ciências Farmacêuticas Básica e Aplicada, v. 35, n. 2, p. 277-282, 2014.
1808-4532
http://hdl.handle.net/11449/133661
ISSN1808-4532-2014-35-02-277-282.pdf
7210986679442751
4006598610021833
url http://serv-bib.fcfar.unesp.br/seer/index.php/Cien_Farm/article/view/3143
http://hdl.handle.net/11449/133661
identifier_str_mv Revista de Ciências Farmacêuticas Básica e Aplicada, v. 35, n. 2, p. 277-282, 2014.
1808-4532
ISSN1808-4532-2014-35-02-277-282.pdf
7210986679442751
4006598610021833
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Revista de Ciências Farmacêuticas Básica e Aplicada
0,131
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 277-282
application/pdf
dc.source.none.fl_str_mv Currículo Lattes
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
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