Glutaraldehyde in bio-catalysts design: a useful crosslinker and a versatile tool in enzyme immobilization

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10045/37704
Registro completo de metadatos
Registro completo de metadatos
Campo DCValorIdioma
dc.contributorMateriales Carbonosos y Medio Ambientees
dc.contributor.authorBarbosa, Oveimar-
dc.contributor.authorOrtiz, Claudia-
dc.contributor.authorBerenguer-Murcia, Ángel-
dc.contributor.authorTorres, Rodrigo-
dc.contributor.authorRodrigues, Rafael C.-
dc.contributor.authorFernández Lafuente, Roberto-
dc.contributor.otherUniversidad de Alicante. Departamento de Química Inorgánicaes
dc.contributor.otherUniversidad de Alicante. Instituto Universitario de Materialeses
dc.date.accessioned2014-05-28T11:21:09Z-
dc.date.available2014-05-28T11:21:09Z-
dc.date.issued2014-
dc.identifier.citationRSC Advances. 2014, 4, 1583-1600. doi:10.1039/C3RA45991Hes
dc.identifier.issn2046-2069-
dc.identifier.urihttp://hdl.handle.net/10045/37704-
dc.description.abstractGlutaraldehyde is one of the most widely used reagents in the design of biocatalysts. It is a powerful crosslinker, able to react with itself, with the advantages that this may bring forth. In this review, we intend to give a general vision of its potential and the precautions that must be taken when using this effective reagent. First, the chemistry of the glutaraldehyde/amino reaction will be commented upon. This reaction is still not fully clarified, but it seems to be based on the formation of 6-membered heterocycles formed by 5 C and one O. Then, we will discuss the production of intra- and inter-molecular enzyme crosslinks (increasing enzyme rigidity or preventing subunit dissociation in multimeric enzymes). Special emphasis will be placed on the preparation of cross-linked enzyme aggregates (CLEAs), mainly in enzymes that have low density of surface reactive groups and, therefore, may be problematic to obtain a final solid catalyst. Next, we will comment on the uses of glutaraldehyde in enzymes previously immobilized on supports. First, the treatment of enzymes immobilized on supports that cannot react with glutaraldehyde (only inter and intramolecular cross-linkings will be possible) to prevent enzyme leakage and obtain some enzyme stabilization via cross-linking. Second, the cross-linking of enzymes adsorbed on aminated supports, where together with other reactions enzyme/support crosslinking is also possible; the enzyme is incorporated into the support. Finally, we will present the use of aminated supports preactivated with glutaraldehyde. Optimal glutaraldehyde modifications will be discussed in each specific case (one or two glutaraldehyde molecules for amino group in the support and/or the protein). Using preactivated supports, the heterofunctional nature of the supports will be highlighted, with the drawbacks and advantages that the heterofunctionality may have. Particular attention will be paid to the control of the first event that causes the immobilization depending on the experimental conditions to alter the enzyme orientation regarding the support surface. Thus, glutaraldehyde, an apparently old fashioned reactive, remains the most widely used and with broadest application possibilities among the compounds used for the design of biocatalyst.es
dc.languageenges
dc.publisherRoyal Society of Chemistryes
dc.rights© Royal Society of Chemistry 2014es
dc.subjectGlutaraldehydees
dc.subjectBio-catalysts designes
dc.subjectCrosslinkeres
dc.subjectEnzyme immobilizationes
dc.subject.otherQuímica Inorgánicaes
dc.titleGlutaraldehyde in bio-catalysts design: a useful crosslinker and a versatile tool in enzyme immobilizationes
dc.typeinfo:eu-repo/semantics/articlees
dc.peerreviewedsies
dc.identifier.doi10.1039/C3RA45991H-
dc.relation.publisherversionhttp://dx.doi.org/10.1039/C3RA45991Hes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
Aparece en las colecciones:INV - MCMA - Artículos de Revistas

Archivos en este ítem:
Archivos en este ítem:
Archivo Descripción TamañoFormato 
Thumbnail2014_Barbosa_etal_RSC-Advances.pdfVersión final (acceso restringido)1,8 MBAdobe PDFAbrir    Solicitar una copia
Thumbnail2014_Barbosa_etal_RSC-Advances_preprint.pdfPreprint (acceso abierto)1,84 MBAdobe PDFAbrir Vista previa


Todos los documentos en RUA están protegidos por derechos de autor. Algunos derechos reservados.