Purification of green fluorescent protein using fast centrifugal partition chromatography

Detalhes bibliográficos
Autor(a) principal: Soares, Bruna P.
Data de Publicação: 2020
Outros Autores: Santos, João H. P. M., Martins, Margarida, Almeida, Mafalda R., Santos, Nathalia V., Freire, Mara G., Santos-Ebinuma, Valéria C., Coutinho, João A. P., Pereira, Jorge F. B., Ventura, Sónia P. M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/30182
Resumo: The green fluorescent protein (GFP) is a biomolecule used in many biological applications such as biomarkers and biosensors, which require high purity levels. It is usually obtained from recombinant Escherichia coli strains, which also produces other endogenous proteins, demanding multiple purification steps, and consequently, increasing the overall costs to obtain pure GFP. Simpler and cheaper purification methods like Aqueous Biphasic Systems (ABS) were already successfully applied to purify GFP at lab scale. Therefore, the development of automatized industrially compatible purification platforms, such as countercurrent chromatography using ABS, can potentially improve the GFP production. This work studied the continuous purification of the variant enhanced GFP (EGFP) by applying ABS composed of polyethylene glycol (PEG 8000), sodium polyacrylate (NaPA 8000) and sodium sulfate (Na2SO4) as electrolyte. An initial screening was carried by changing the electrolyte content in the ABS. The increase of this condition has demonstrated an increase on the EGFP partition for the PEG-rich phase. The most efficient ABS and, at the same time, with the most appropriate conditions, namely the system composed of 15 wt% PEG 8000 + 4.5 wt% NaPA 8000 + 2.5 wt% Na2SO4 was chosen and applied on the fast centrifugal partition chromatography (FCPC). After optimization, the best operational conditions were identified, i.e. a flow rate of 2.5 mL.min−1 and rotation speed of 2000 rpm at ascending mode, and the best results obtained, meaning a purification of 89.93% and a recovery yield of 82.3%, confirming the potential of FCPC to the continuous purification of EGFP.
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spelling Purification of green fluorescent protein using fast centrifugal partition chromatographyAqueous biphasic systemsElectrolyteEnhanced green fluorescent proteinFast centrifugal partition chromatographyPurificationThe green fluorescent protein (GFP) is a biomolecule used in many biological applications such as biomarkers and biosensors, which require high purity levels. It is usually obtained from recombinant Escherichia coli strains, which also produces other endogenous proteins, demanding multiple purification steps, and consequently, increasing the overall costs to obtain pure GFP. Simpler and cheaper purification methods like Aqueous Biphasic Systems (ABS) were already successfully applied to purify GFP at lab scale. Therefore, the development of automatized industrially compatible purification platforms, such as countercurrent chromatography using ABS, can potentially improve the GFP production. This work studied the continuous purification of the variant enhanced GFP (EGFP) by applying ABS composed of polyethylene glycol (PEG 8000), sodium polyacrylate (NaPA 8000) and sodium sulfate (Na2SO4) as electrolyte. An initial screening was carried by changing the electrolyte content in the ABS. The increase of this condition has demonstrated an increase on the EGFP partition for the PEG-rich phase. The most efficient ABS and, at the same time, with the most appropriate conditions, namely the system composed of 15 wt% PEG 8000 + 4.5 wt% NaPA 8000 + 2.5 wt% Na2SO4 was chosen and applied on the fast centrifugal partition chromatography (FCPC). After optimization, the best operational conditions were identified, i.e. a flow rate of 2.5 mL.min−1 and rotation speed of 2000 rpm at ascending mode, and the best results obtained, meaning a purification of 89.93% and a recovery yield of 82.3%, confirming the potential of FCPC to the continuous purification of EGFP.Elsevier2020-12-18T15:49:46Z2023-02-15T00:00:00Z2021-02-15T00:00:00Z2021-02-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentapplication/vnd.openxmlformats-officedocument.wordprocessingml.documenthttp://hdl.handle.net/10773/30182eng1383-586610.1016/j.seppur.2020.117648Soares, Bruna P.Santos, João H. P. M.Martins, MargaridaAlmeida, Mafalda R.Santos, Nathalia V.Freire, Mara G.Santos-Ebinuma, Valéria C.Coutinho, João A. P.Pereira, Jorge F. B.Ventura, Sónia P. M.info:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T11:58:22Zoai:ria.ua.pt:10773/30182Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:02:21.308076Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Purification of green fluorescent protein using fast centrifugal partition chromatography
title Purification of green fluorescent protein using fast centrifugal partition chromatography
spellingShingle Purification of green fluorescent protein using fast centrifugal partition chromatography
Soares, Bruna P.
Aqueous biphasic systems
Electrolyte
Enhanced green fluorescent protein
Fast centrifugal partition chromatography
Purification
title_short Purification of green fluorescent protein using fast centrifugal partition chromatography
title_full Purification of green fluorescent protein using fast centrifugal partition chromatography
title_fullStr Purification of green fluorescent protein using fast centrifugal partition chromatography
title_full_unstemmed Purification of green fluorescent protein using fast centrifugal partition chromatography
title_sort Purification of green fluorescent protein using fast centrifugal partition chromatography
author Soares, Bruna P.
author_facet Soares, Bruna P.
Santos, João H. P. M.
Martins, Margarida
Almeida, Mafalda R.
Santos, Nathalia V.
Freire, Mara G.
Santos-Ebinuma, Valéria C.
Coutinho, João A. P.
Pereira, Jorge F. B.
Ventura, Sónia P. M.
author_role author
author2 Santos, João H. P. M.
Martins, Margarida
Almeida, Mafalda R.
Santos, Nathalia V.
Freire, Mara G.
Santos-Ebinuma, Valéria C.
Coutinho, João A. P.
Pereira, Jorge F. B.
Ventura, Sónia P. M.
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Soares, Bruna P.
Santos, João H. P. M.
Martins, Margarida
Almeida, Mafalda R.
Santos, Nathalia V.
Freire, Mara G.
Santos-Ebinuma, Valéria C.
Coutinho, João A. P.
Pereira, Jorge F. B.
Ventura, Sónia P. M.
dc.subject.por.fl_str_mv Aqueous biphasic systems
Electrolyte
Enhanced green fluorescent protein
Fast centrifugal partition chromatography
Purification
topic Aqueous biphasic systems
Electrolyte
Enhanced green fluorescent protein
Fast centrifugal partition chromatography
Purification
description The green fluorescent protein (GFP) is a biomolecule used in many biological applications such as biomarkers and biosensors, which require high purity levels. It is usually obtained from recombinant Escherichia coli strains, which also produces other endogenous proteins, demanding multiple purification steps, and consequently, increasing the overall costs to obtain pure GFP. Simpler and cheaper purification methods like Aqueous Biphasic Systems (ABS) were already successfully applied to purify GFP at lab scale. Therefore, the development of automatized industrially compatible purification platforms, such as countercurrent chromatography using ABS, can potentially improve the GFP production. This work studied the continuous purification of the variant enhanced GFP (EGFP) by applying ABS composed of polyethylene glycol (PEG 8000), sodium polyacrylate (NaPA 8000) and sodium sulfate (Na2SO4) as electrolyte. An initial screening was carried by changing the electrolyte content in the ABS. The increase of this condition has demonstrated an increase on the EGFP partition for the PEG-rich phase. The most efficient ABS and, at the same time, with the most appropriate conditions, namely the system composed of 15 wt% PEG 8000 + 4.5 wt% NaPA 8000 + 2.5 wt% Na2SO4 was chosen and applied on the fast centrifugal partition chromatography (FCPC). After optimization, the best operational conditions were identified, i.e. a flow rate of 2.5 mL.min−1 and rotation speed of 2000 rpm at ascending mode, and the best results obtained, meaning a purification of 89.93% and a recovery yield of 82.3%, confirming the potential of FCPC to the continuous purification of EGFP.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-18T15:49:46Z
2021-02-15T00:00:00Z
2021-02-15
2023-02-15T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/30182
url http://hdl.handle.net/10773/30182
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 1383-5866
10.1016/j.seppur.2020.117648
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dc.format.none.fl_str_mv application/vnd.openxmlformats-officedocument.wordprocessingml.document
application/vnd.openxmlformats-officedocument.wordprocessingml.document
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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