4.5 Article

Enzyme stabilization by glutaraldehyde crosslinking of adsorbed proteins on aminated supports

Journal

JOURNAL OF BIOTECHNOLOGY
Volume 119, Issue 1, Pages 70-75

Publisher

ELSEVIER
DOI: 10.1016/j.jbiotec.2005.05.021

Keywords

glucose oxidase; glutaryl acylase; D-Amino acid oxidase; glutaraldehyde; enzyme stabilization; enzyme immobilization

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The stabilization achieved by different immobilization protocols have been compared using three different enzymes (glutaryl acylase (GAC), D-aminoacid oxidase (DAAO), and glucose oxidase (GOX)): adsorption on animated supports, treatment of this adsorbed enzymes with glutaraldehyde, and immobilization on glutaraldehyde pre-activated supports. In all cases, the treatment of adsorbed enzymes on amino-supports with glutaraldehyde yielded the higher stabilizations: in the case of GOX, a stabilization over 400-fold was achieved. After this treatment, the enzymes could no longer be desorbed from the supports using high ionic strength (suggesting the support-protein reaction). Modification of the enzymes immobilized on supports that did not offer the possibility of react with glutaraldehyde showed the same stability that the non modified preparations demonstrating that the mere chemical modification did not have effect on the enzyme stability. This simple strategy seems to permit very good results in terms of immobilization rate and stability, offering some advantages when compared to the immobilization on glutaraldehyde pre-activated supports. (c) 2005 Elsevier B.V. All rights reserved.

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