Stabilization of Candida antarctica Lipase B (CALB) Immobilized on Octyl Agarose by Treatment with Polyethyleneimine (PEI)

• Published in: Molecules
• Main Authors: Peirce, Sara, Tacias-Pascacio, Veymar G., Russo, María Elena, Marzocchella, Antonio, Virgen-Ortíz, José J., Fernández-Lafuente, Roberto
• Other Authors: Ministerio de Economía y Competitividad (España), Università degli Studi di Napoli Federico II, Consejo Nacional de Ciencia y Tecnología (México), Consejo Superior de Investigaciones Científicas (España)
• Format: Article in Journal/Newspaper
• Language: unknown
• Published: Multidisciplinary Digital Publishing Institute 2016
• Subjects: Triton; Antarc*; Antarctica
• Online Access: http://hdl.handle.net/10261/142084; https://doi.org/10.3390/molecules21060751; https://doi.org/10.13039/501100003329; https://doi.org/10.13039/100007195; https://doi.org/10.13039/501100003141; https://doi.org/10.13039/501100003339

Lipase B from Candida antarctica (CALB) was immobilized on octyl agarose (OC) and physically modified with polyethyleneimine (PEI) in order to confer a strong ion exchange character to the enzyme and thus enable the immobilization of other enzymes on its surface. The enzyme activity was fully maintained during the coating and the thermal stability was marginally improved. The enzyme release from the support by incubation in the non-ionic detergent Triton X-100 was more difficult after the PEI-coating, suggesting that some intermolecular physical crosslinking had occurred, making this desorption more difficult. Thermal stability was marginally improved, but the stability of the OCCALB-PEI was significantly better than that of OCCALB during inactivation in mixtures of aqueous buffer and organic cosolvents. SDS-PAGE analysis of the inactivated biocatalyst showed the OCCALB released some enzyme to the medium during inactivation, and this was partially prevented by coating with PEI. This effect was obtained without preventing the possibility of reuse of the support by incubation in 2% ionic detergents. That way, this modified CALB not only has a strong anion exchange nature, while maintaining the activity, but it also shows improved stability under diverse reaction conditions without affecting the reversibility of the immobilization. We thank the support from MINECO, grant CTQ2013-41507-R. The predoctoral fellowships for Miss Peirce (Universita’ degli Studi di Napoli Federico II) and Miss Tacias-Pascacio (CONACyT, Mexico) are also gratefully recognized. Virgen-Ortíz thanks CONACyT Mexico for his Postdoctoral fellowship (No. 263815). We acknowledge support by the CSIC Open Access Publication Initiative through its Unit of Information Resources for Research (URICI).