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Extraction of recombinant proteins from Escherichia coli by cell disruption with aqueous solutions of surface-active compounds

dc.contributor.authorMartins, Margarida
dc.contributor.authorOoi, Chien Wei
dc.contributor.authorNeves, Márcia C
dc.contributor.authorPereira, Jorge F B [UNESP]
dc.contributor.authorCoutinho, João A P
dc.contributor.authorVentura, Sónia P M
dc.contributor.institutionUniversity of Aveiro
dc.contributor.institutionJalan Lagoon Selatan
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T16:52:29Z
dc.date.available2018-12-11T16:52:29Z
dc.date.issued2018-07-01
dc.description.abstractBACKGROUND: Green fluorescent protein (GFP) is used extensively as a biomarker due to its unique spectral and fluorescence characteristics. GFP is usually obtained from recombinant strains of Escherichia coli (E. coli) producing the protein intracellularly. However, the common methods of extraction are cumbersome leading to an increase in the downstream process costs and complexity, sometimes leading to a higher risk of biomolecule degradation. RESULTS: This work proposes a new method to extract recombinant intracellular GFP from E. coli BL21 by using aqueous solutions of surface-active compounds. CONCLUSION: By comparing the fluorescence intensity of the extracted GFP, it was concluded that some of these compounds, namely ionic liquids with an alkyl chain of 10 or more carbons (best solvent being tributyl-1-tetradecylphosphonium, [P4,4,4,14]Cl) are more effective than an ultrasonic-assisted extraction, even at low concentrations, being able to extract the whole GFP content from the cells. © 2018 Society of Chemical Industry.en
dc.description.affiliationCICECO - Aveiro Institute of Materials Department of Chemistry University of Aveiro
dc.description.affiliationChemical Engineering Discipline School of Engineering Monash University Malaysia Jalan Lagoon Selatan
dc.description.affiliationUniversidade Estadual Paulista (UNESP) School of Pharmaceutical Sciences Campus (Araraquara) Department of Bioprocesses and Biotechnology
dc.description.affiliationUnespUniversidade Estadual Paulista (UNESP) School of Pharmaceutical Sciences Campus (Araraquara) Department of Bioprocesses and Biotechnology
dc.description.sponsorshipMinistério da Ciência, Tecnologia e Inovação
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipFundação para a Ciência e a Tecnologia
dc.description.sponsorshipIdMinistério da Ciência, Tecnologia e Inovação: 02-02-10-SF0290
dc.description.sponsorshipIdFAPESP: 2014/16424-7
dc.description.sponsorshipIdFundação para a Ciência e a Tecnologia: 2014/19793-3
dc.format.extent1864-1870
dc.identifierhttp://dx.doi.org/10.1002/jctb.5596
dc.identifier.citationJournal of Chemical Technology and Biotechnology, v. 93, n. 7, p. 1864-1870, 2018.
dc.identifier.doi10.1002/jctb.5596
dc.identifier.issn1097-4660
dc.identifier.issn0268-2575
dc.identifier.scopus2-s2.0-85044238315
dc.identifier.urihttp://hdl.handle.net/11449/170804
dc.language.isoeng
dc.relation.ispartofJournal of Chemical Technology and Biotechnology
dc.relation.ispartofsjr0,766
dc.rights.accessRightsAcesso restritopt
dc.sourceScopus
dc.subjectcell disruption
dc.subjectextraction
dc.subjectgreen fluorescent protein
dc.subjectintracellular protein
dc.subjectrecombinant proteins
dc.subjectsurface-active compounds
dc.titleExtraction of recombinant proteins from Escherichia coli by cell disruption with aqueous solutions of surface-active compoundsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0001-5959-0015[4]
unesp.author.orcid0000-0001-9049-4267[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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