Pseudomonas fluorescens lipase immobilization on polysiloxane–polyvinyl alcohol composite chemically modified with epichlorohydrin

• Published in: Journal of molecular catalysis. B, Enzymatic Vol. 52; pp. 49 - 57
• Main Authors: Santos, J.C., Paula, A.V., Nunes, G.F.M., de Castro, H.F.
• Format: Journal Article Conference Proceeding
• Language: English
• Published: Amsterdam Elsevier B.V 01-06-2008; Elsevier Science
• Subjects: Biological and medical sciences; Biotechnology; Enzyme immobilization; Epichlorohydrin; Fundamental and applied biological sciences. Psychology; Glutaraldehyde; Immobilization of enzymes and other molecules; Immobilization techniques; Lipase; Methods. Procedures. Technologies; Polysiloxane–polyvinyl alcohol; Epichlorohydrin; Polysiloxane–polyvinyl alcohol; Enzyme immobilization; Glutaraldehyde; Lipase; Pseudomonadales; Enzyme; Epichlorhydrin; Immobilization; Triacylglycerol lipase; Esterases; Pseudomonas fluorescens; Glutaral; Polysiloxane-polyvinyl alcohol; Carboxylic ester hydrolases; Polyvinylalcohol; Chemical modification; Bacteria; Hydrolases; Pseudomonadaceae; Siloxane polymer
• ISSN: 1381-1177; 1873-3158
• DOI: 10.1016/j.molcatb.2007.11.005

The technique based on sol–gel approach was used to generate silica matrices derivatives by hydrolysis of silane compounds. The present work evaluates a hybrid matrix obtained with tetraethoxysilane (TEOS) and polyvinyl alcohol (PVA) on the immobilization yield of lipase from
Pseudomonas fluorescens. The resulting polysiloxane–polyvinyl alcohol (POS–PVA) matrix combines the property of PVA as a suitable polymer to retain proteins with an excellent optical, thermal and chemical stability of the host silicon oxide matrix. Aiming to render adequate functional groups to the covalent binding with the enzyme the POS–PVA matrix was chemically modified using epichlorohydrin. The results were compared with immobilized derivative on POS–PVA activated with glutaraldehyde. Immobilization yield based on the recovered lipase activity depended on the activating agent and the highest efficiency (32%) was attained when lipase was immobilized on POS–PVA activated with epichlorohydrin, which, probably, provided more linkage points for the covalent bind of the enzyme on the support. This was confirmed by determining the morphological properties using different techniques as X-ray diffraction and scanning electron microscopy (SEM). Comparative studies were carried out to attain optimal activities for free lipase and immobilized systems. For this purpose, a central composite experimental design with different combinations of pH and temperature was performed. Enzymatic hydrolysis with the immobilized enzyme in the framework of the Michaelis–Menten mechanism was also reported. Under optimum conditions, the immobilized derivative on POS–PVA activated with epichlorohydrin showed to have more affinity for the substrate in the hydrolysis of olive oil, with a Michaelis–Menten constant value (
K
m) of 293
mM, compared to the value of 401
mM obtained for the immobilized lipase on support activated with glutaraldehyde. Data generated by DSC showed that both immobilized derivatives have similar thermal stabilities.