Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/30128
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dc.contributor.authorSeručnik, Mojcapt_PT
dc.contributor.authorVicente, Filipa A.pt_PT
dc.contributor.authorBrečko, Živapt_PT
dc.contributor.authorCoutinho, João A. P.pt_PT
dc.contributor.authorVentura, Sónia P. M.pt_PT
dc.contributor.authorŽnidaršič-Plazl, Polonapt_PT
dc.date.accessioned2020-12-17T10:41:23Z-
dc.date.available2020-12-17T10:41:23Z-
dc.date.issued2020-11-11-
dc.identifier.issn2168-0485pt_PT
dc.identifier.urihttp://hdl.handle.net/10773/30128-
dc.description.abstractTemperature-dependent aqueous micellar two-phase systems (AMTPSs) have recently been gaining attention in the isolation of high-added-value biomolecules from their natural sources. Despite their sustainability, aqueous two-phase systems, and particularly AMTPSs, have not been extensively applied in the industry, which might be changed by applying process integration and continuous manufacturing. Here, we report for the first time on an integrated microfluidic platform for fast and low-material-consuming development of continuous protein purification using an AMTPS. A system comprised of a microchannel incubated at high temperature, enabling instantaneous triggering of a two-phase system formation, and a microsettler, allowing complete phase separation at the outlets, is reported here. The separation of phycobiliproteins and particularly the purification of R-phycoerythrin from the contaminant proteins present in the aqueous crude extract obtained from fresh cells of Gracilaria gracilis were thereby achieved. The results from the developed microfluidic system revealed that the fractionation performance was maintained while reducing the processing time more than 20-fold when compared with the conventional lab-scale batch process. Furthermore, the integration of a miniaturized ultrafiltration module resulted in the complete removal of the surfactant from the bottom phase containing R-phycoerythrin, as well as in nearly twofold target protein concentration. The process setup successfully exploits the benefits of process intensification along with the integration of various downstream processes. Further transfer to a meso-scale integrated system would make such a system appropriate for the separation and purification of biomolecules with high commercial interest.pt_PT
dc.language.isoengpt_PT
dc.publisherAmerican Chemical Societypt_PT
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/811040/EUpt_PT
dc.relationUIDB/50011/2020pt_PT
dc.relationUIDP/50011/2020pt_PT
dc.relationIF/00402/2015pt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectAqueous micellar two-phase systemsproteinpt_PT
dc.subjectMicrofluidicspt_PT
dc.subjectProcess intensificationpt_PT
dc.subjectSeparationpt_PT
dc.subjectUltrafiltrationpt_PT
dc.titleDevelopment of a microfluidic platform for R-Phycoerythrin purification using an aqueous micellar two-Phase systempt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.firstPage17097pt_PT
degois.publication.issue46pt_PT
degois.publication.lastPage17105pt_PT
degois.publication.titleACS Sustainable Chemistry & Engineeringpt_PT
degois.publication.volume8pt_PT
dc.identifier.doi10.1021/acssuschemeng.0c05042pt_PT
dc.identifier.essn2168-0485pt_PT
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