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Designing tailor-made steric matters to improve the immobilized ficin specificity for small versus large proteins

dc.contributor.authorSiar, El Hocine
dc.contributor.authorAbellanas Pérez, Pedro
dc.contributor.authorMorellon Sterling, Roberto
dc.contributor.authorBolívar Bolívar, Juan Manuel
dc.contributor.authorRocha Martín, Javier
dc.contributor.authorFernandez Lafuente, Roberto
dc.date.accessioned2024-12-03T09:39:40Z
dc.date.available2024-12-03T09:39:40Z
dc.date.issued2024
dc.descriptionThis research was funded by Ministerio de Ciencia e Innovación and Agencia Estatal de Investigación (Spanish Government) (PID2022–136535OB-I00). We gratefully recognize Prof. Ángel Berenguer-Murcia for his suggestions and help during the writing of this paper.
dc.description.abstractThe development of strategies that can permit to adjust the size specificity of immobilized proteases by the generation of steric hindrances may enlarge its applicability. Using as a model ficin immobilized on glyoxyl agarose, two strategies were assayed to generate tailor made steric hindrances. First, ficin has been coimmobilized on supports coated with large proteins (hemoglobin or bovine serum albumin (BSA)). While coimmobilization of ficin with BSA presented no effect on the activity versus any of the assayed substrates, coimmobilization with hemoglobin permitted to improve the immobilized ficin specificity for casein versus hemoglobin, but still significant activity versus hemoglobin remained. Second, aldehyde-dextran has been employed to modify the immobilized ficin, trying to generate steric hindrances to avoid the entry of large proteins (hemoglobin) while enabling the entry of small ones (casein). This also increased the size specificity of ficin, but still did not suppress the activity versus hemoglobin. The combination of both strategies and the use of 37ºC during the proteolysis enabled to almost fully nullify the hydrolytic activity versus hemoglobin while preserving a high percentage of the activity versus casein. The modifications improved enzyme stability and the biocatalyst could be reused for 5 cycles without alteration of its properties.
dc.description.departmentDepto. de Ingeniería Química y de Materiales
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Ciencias Químicas
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia, Innovación y Universidades (España)
dc.description.statuspub
dc.identifier.citationSiar, E. H., Abellanas-Perez, P., Morellon-Sterling, R., Bolivar, J. M., Rocha-Martin, J., & Fernandez-Lafuente, R. (2024). Designing tailor-made steric matters to improve the immobilized ficin specificity for small versus large proteins. Journal of Biotechnology, 395, 12-21. https://doi.org/10.1016/j.jbiotec.2024.09.005
dc.identifier.doi10.1016/j.jbiotec.2024.09.005
dc.identifier.essn1873-4863
dc.identifier.issn0168-1656
dc.identifier.officialurlhttps://doi.org/10.1016/j.jbiotec.2024.09.005
dc.identifier.relatedurlhttps://www.sciencedirect.com/science/article/pii/S0168165624002475?via%3Dihub
dc.identifier.urihttps://hdl.handle.net/20.500.14352/111933
dc.journal.titleJournal of Biotechnology
dc.language.isoeng
dc.page.final21
dc.page.initial12
dc.publisherElsevier
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICIU//PID2022–136535OB-I00/ES
dc.rightsAttribution-NonCommercial 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subject.cdu577.1
dc.subject.cdu577.15
dc.subject.cdu66.098
dc.subject.keywordProtease immobilization
dc.subject.keywordSize specificity tuning
dc.subject.keywordSteric hindrances
dc.subject.ucmBioquímica (Biología)
dc.subject.unesco3302 Tecnología Bioquímica
dc.subject.unesco2403 Bioquímica
dc.subject.unesco2302.09 Enzimología
dc.titleDesigning tailor-made steric matters to improve the immobilized ficin specificity for small versus large proteins
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number395
dspace.entity.typePublication
relation.isAuthorOfPublicationdd41e7a5-3013-4b28-8263-915921ecf30a
relation.isAuthorOfPublication9d7ac6de-a596-4647-a7fa-3a1c143055e4
relation.isAuthorOfPublication.latestForDiscoverydd41e7a5-3013-4b28-8263-915921ecf30a

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