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A Spring in Performance: Silica Nanosprings Boost Enzyme Immobilization in Microfluidic Channels

dc.contributor.authorValikhani, Donya
dc.contributor.authorBolívar Bolívar, Juan Manuel
dc.contributor.authorViefhues, Martina
dc.contributor.authorMcIlroy, David
dc.contributor.authorVrouwe, Elwin
dc.contributor.authorNidetzky, Bernd
dc.date.accessioned2024-01-09T10:36:09Z
dc.date.available2024-01-09T10:36:09Z
dc.date.issued2017
dc.description.abstractEnzyme microreactors are important tools of miniaturized analytics and have promising applications in continuous biomanufacturing. A fundamental problem of their design is that plain microchannels without extensive static internals, or packings, offer limited exposed surface area for immobilizing the enzyme. To boost the immobilization in a manner broadly applicable to enzymes, we coated borosilicate microchannels with silica nanosprings and attached the enzyme, sucrose phosphorylase, via a silica-binding module genetically fused to it. We showed with confocal fluorescence microscopy that the enzyme was able to penetrate the ∼70 μm-thick nanospring layer and became distributed uniformly in it. Compared with the plain surface, the activity of immobilized enzyme was enhanced 4.5-fold upon surface coating with nanosprings and further increased up to 10-fold by modifying the surface of the nanosprings with sulfonate groups. Operational stability during continuous-flow biocatalytic synthesis of α-glucose 1-phosphate was improved by a factor of 11 when the microreactor coated with nanosprings was used. More than 85% of the initial conversion rate was retained after 840 reactor cycles performed with a single loading of enzyme. By varying the substrate flow rate, the microreactor performance was conveniently switched between steady states of quantitative product yield (50 mM) and optimum productivity (19 mM min–1) at a lower product yield of 40%. Surface coating with silica nanosprings thus extends the possibilities for enzyme immobilization in microchannels. It effectively boosts the biocatalytic function of a microstructured reactor limited otherwise by the solid surface available for immobilizing the enzyme.
dc.description.departmentDepto. de Ingeniería Química y de Materiales
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipEuropean Commission
dc.description.sponsorshipUnited States Office of Naval Research
dc.description.statuspub
dc.identifier.citationValikhani, D., Bolivar, J. M., Viefhues, M., McIlroy, D. N., Vrouwe, E. X., & Nidetzky, B. (2017). A Spring in Performance: Silica Nanosprings Boost Enzyme Immobilization in Microfluidic Channels. ACS Applied Materials and Interfaces, 9(40), 34641-34649. https://doi.org/10.1021/ACSAMI.7B09875
dc.identifier.doi10.1021/acsami.7b09875
dc.identifier.essn1944-8252
dc.identifier.issn1944-8244
dc.identifier.officialurlhttps://doi.org/10.1021/acsami.7b09875
dc.identifier.urihttps://hdl.handle.net/20.500.14352/91976
dc.issue.number40
dc.journal.titleACS Applied Materials and Interfaces
dc.language.isoeng
dc.page.final34649
dc.page.initial34641
dc.publisherAmerican Chemical Society
dc.relation.projectIDMarie Curie ITN project EUROMBR, Grant 608104
dc.relation.projectIDGrant N00014-16-1-2277
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.cdu66.0
dc.subject.cdu577.1
dc.subject.keywordSurface modificacion
dc.subject.keywordSilica nanosprings
dc.subject.keywordMicroreactor
dc.subject.keywordBiocatalysis
dc.subject.keywordEnzyme immobilization
dc.subject.ucmQuímica industrial
dc.subject.ucmIngeniería química
dc.subject.ucmBioquímica (Química)
dc.subject.ucmBiotecnología
dc.subject.unesco2302 Bioquímica
dc.subject.unesco3302 Tecnología Bioquímica
dc.subject.unesco3303 Ingeniería y Tecnología Químicas
dc.titleA Spring in Performance: Silica Nanosprings Boost Enzyme Immobilization in Microfluidic Channels
dc.typejournal article
dc.type.hasVersionAM
dc.volume.number9
dspace.entity.typePublication
relation.isAuthorOfPublicationdd41e7a5-3013-4b28-8263-915921ecf30a
relation.isAuthorOfPublication.latestForDiscoverydd41e7a5-3013-4b28-8263-915921ecf30a

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