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Support Enzyme Loading Influences the Effect of Aldehyde Dextran Modification on the Specificity of Immobilized Ficin for Large Proteins

dc.contributor.authorSiar, El Hocine
dc.contributor.authorAbellanas Pérez, Pedro
dc.contributor.authorRocha Martín, Javier
dc.contributor.authorFernández Lafuente, Roberto
dc.date.accessioned2024-12-10T09:01:08Z
dc.date.available2024-12-10T09:01:08Z
dc.date.issued2024
dc.description.abstractIt has been reported that the modification of immobilized glyoxyl–ficin with aldehyde dextran can promote steric hindrances that greatly reduce the activity of the immobilized protease against hemoglobin, while the protease still maintained a reasonable level of activity against casein. In this paper, we studied if this effect may be different depending on the amount of ficin loaded on the support. For this purpose, both the moderately loaded and the overloaded glyoxyl–ficin biocatalysts were prepared and modified with aldehyde dextran. While the moderately loaded biocatalyst had a significantly reduced activity, mainly against hemoglobin, the activity of the overloaded biocatalyst was almost maintained. This suggests that aldehyde dextran was able to modify areas of the moderately loaded enzyme that were not available when the enzyme was overloaded. This modification promoted a significant increase in biocatalyst stability for both biocatalysts, but the stability was higher for the overloaded biocatalyst (perhaps due to a combination of inter- and intramolecular crosslinking).
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipAgencia Estatal de Investigación (España)
dc.description.statuspub
dc.identifier.citationSiar, E. H., Abellanas-Perez, P., Rocha-Martin, J., & Fernandez-Lafuente, R. (2024). Support Enzyme Loading Influences the Effect of Aldehyde Dextran Modification on the Specificity of Immobilized Ficin for Large Proteins. Molecules, 29(15). https://doi.org/10.3390/MOLECULES29153674
dc.identifier.doi10.3390/molecules29153674
dc.identifier.essn1420-3049
dc.identifier.officialurlhttps://doi.org/10.3390/molecules29153674
dc.identifier.relatedurlhttps://www.mdpi.com/1420-3049/29/15/3674
dc.identifier.urihttps://hdl.handle.net/20.500.14352/112286
dc.issue.number15
dc.journal.titleMolecules
dc.language.isoeng
dc.page.final13
dc.page.initial1
dc.publisherMDPI
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2022-136535OB-I00/NTEGRACION DE NANOTECNOLOGIA Y DISEÑO DE BIOCATALIZADORES: NUEVAS ESTRATEGIAS PARA ABORDAR LOS PROBLEMAS DE LA COIMMOVILIZACION DE ENZIMAS
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu577.1
dc.subject.cdu577.152.34
dc.subject.cdu577.2
dc.subject.cdu544.47
dc.subject.keywordSteric hindrances
dc.subject.keywordSize specificity
dc.subject.keywordTuning enzyme specificity
dc.subject.keywordEnzyme loading
dc.subject.keywordImmobilized proteases
dc.subject.ucmBioquímica (Biología)
dc.subject.ucmBiología molecular (Biología)
dc.subject.unesco2403 Bioquímica
dc.subject.unesco2302.09 Enzimología
dc.subject.unesco2210.01 Catálisis
dc.subject.unesco2415 Biología Molecular
dc.titleSupport Enzyme Loading Influences the Effect of Aldehyde Dextran Modification on the Specificity of Immobilized Ficin for Large Proteins
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number29
dspace.entity.typePublication
relation.isAuthorOfPublication9d7ac6de-a596-4647-a7fa-3a1c143055e4
relation.isAuthorOfPublication9d7ac6de-a596-4647-a7fa-3a1c143055e4
relation.isAuthorOfPublication.latestForDiscovery9d7ac6de-a596-4647-a7fa-3a1c143055e4

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