Taguchi orthogonal design assisted immobilization of Candida rugosa lipase onto nanocellulose-silica reinforced polyethersulfone membrane: physicochemical characterization and operational stability

A greener processing route to replace the current environmentally-unfriendly esterification technique to produce biofuels such as pentyl valerate (PeVa) was explored. This study statistically optimized the covalent immobilization of Candida rugosa lipase (CRL) onto biomass-based nanocellulose-silica...

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Main Authors: Elias, Nursyafiqah, Abdul Wahab, Roswanira, Lau, Woei Jye, Mahat, Naji Arafat, Chandren, Sheela, Jamalis, Joazaizulfazli
Format: Article
Published: Springer Science and Business Media B.V. 2021
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Online Access:http://eprints.utm.my/id/eprint/95774/
http://dx.doi.org/10.1007/s10570-021-03886-8
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Summary:A greener processing route to replace the current environmentally-unfriendly esterification technique to produce biofuels such as pentyl valerate (PeVa) was explored. This study statistically optimized the covalent immobilization of Candida rugosa lipase (CRL) onto biomass-based nanocellulose-silica (NC-SiO2) reinforced polyethersulfone (PES) membrane to synthesize PeVa. Raman spectroscopy, field emission scanning electron microscopy, high-resolution transmission electron microscopy, and atomic force microscopy of NC-SiO2-PES/CRL proved that CRL was successfully conjugated to the membrane. The optimized Taguchi Design-assisted immobilization of CRL onto NC-SiO2-PES membrane (5% glutaraldehyde, 4 h of immobilization, 20 mg/mL CRL concentration, 40 °C and pH 5) gave 90% yield of PeVa in 3 h. The thermal stability of NC-SiO2-PES/CRL was ~ 30% greater over the free CRL, with reusability for up to 14 successive esterification cycles. In a nutshell, the greener NC-SiO2-PES membrane effectively hyperactivated and stabilized the CRL for the esterification production of PeVa. This research provides a promising approach for expanding the use of sustainably sourced NC and SiO2 nanoparticles, as fillers in a PES for improving CRL activity and durability for an extended catalytic process. Graphical abstract: [Figure not available: see fulltext.].