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Evaluation of Styrene-Divinylbenzene Beads as a Support to Immobilize Lipases

A commercial and very hydrophobic styrene-divinylbenzene matrix, MCI GEL(®) CHP20P, has been compared to octyl-Sepharose(®) beads as support to immobilize three different enzymes: lipases from Thermomyces lanuginosus (TLL) and from Rhizomucor miehie (RML) and Lecitase(®) Ultra, a commercial artifici...

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Detalles Bibliográficos
Autores principales: Garcia-Galan, Cristina, Barbosa, Oveimar, Hernandez, Karel, dos Santos, Jose C. S., Rodrigues, Rafael C., Fernandez-Lafuente, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271320/
https://www.ncbi.nlm.nih.gov/pubmed/24918537
http://dx.doi.org/10.3390/molecules19067629
Descripción
Sumario:A commercial and very hydrophobic styrene-divinylbenzene matrix, MCI GEL(®) CHP20P, has been compared to octyl-Sepharose(®) beads as support to immobilize three different enzymes: lipases from Thermomyces lanuginosus (TLL) and from Rhizomucor miehie (RML) and Lecitase(®) Ultra, a commercial artificial phospholipase. The immobilization mechanism on both supports was similar: interfacial activation of the enzymes versus the hydrophobic surface of the supports. Immobilization rate and loading capacity is much higher using MCI GEL(®) CHP20P compared to octyl-Sepharose(®) (87.2 mg protein/g of support using TLL, 310 mg/g using RML and 180 mg/g using Lecitase(®) Ultra). The thermal stability of all new preparations is much lower than that of the standard octyl-Sepharose(®) immobilized preparations, while the opposite occurs when the inactivations were performed in the presence of organic co-solvents. Regarding the hydrolytic activities, the results were strongly dependent on the substrate and pH of measurement. Octyl-Sepharose(®) immobilized enzymes were more active versus p-NPB than the enzymes immobilized on MCI GEL(®) CHP20P, while RML became 700-fold less active versus methyl phenylacetate. Thus, the immobilization of a lipase on this matrix needs to be empirically evaluated, since it may present very positive effects in some cases while in other cases it may have very negative ones.