Enhanced Biodiesel Production with Eversa Transform 2.0 Lipase on Magnetic Nanoparticles.

Langmuir

Instituto de Engenharia e Desenvolvimento Sustentável - IEDS, Campus das Auroras, Universidade da Integração Internacional da Lusofonia Afro-Brasileira - UNILAB, Rua José Franco de Oliveira, s/n - Zona Rural, Redenção 62790-970, CE, Brazil.

Published: December 2024

AI Article Synopsis

  • This research explores using magnetic iron oxide nanoparticles to immobilize the lipase enzyme ET 2.0 for enhanced biodiesel production through the synthesis of ethyl oleate.
  • The study optimized conditions for enzyme immobilization, achieving a yield of 78% and demonstrating higher performance from the immobilized enzyme compared to its free form.
  • Kinetic studies confirmed successful esterification with 88.1% conversion and sustainable production, while molecular docking suggested strong stability and binding affinity between the lipase and the substrate.

Article Abstract

This research investigated the usefulness of magnetic iron oxide nanoparticles (FeO) as a support to immobilize the lipase Eversa Transform 2.0 (ET 2.0) to obtain an active and stable biocatalyst, easily recoverable from the reaction medium for applications in the production of biodiesel. Biodiesel was an alternative fuel composed mainly of fatty acid esters with strong transesterification and esterification capabilities. The study focused on the esterification of oleic acid with ethanol to synthesize ethyl oleate. Magnetic nanoparticles were prepared by coprecipitation, then activated with glutaraldehyde and functionalized with γ-aminopropyltriethoxysilane (APTES). The optimal conditions for immobilizing ET 2.0 were pH 10, 25 mM sodium carbonate buffer, an enzymatic load of 200 U/g, and 1 h of contact time, obtaining 78% yield and enzymatic activity of 205.9 U/g. Postimmobilization evaluation showed that the immobilized enzyme performed better than its free form. Kinetic studies were conducted under these optimized conditions (2-96 h at 150 rpm and 37 °C). The biocatalyst was tested for the synthesis of ethyl oleate using oleic acid as the substrate and ethanol, achieving a conversion of 88.1%. Subsequent recirculation tests maintained approximately 80% conversion until the fourth cycle, confirming the sustainability of ester production. Molecular docking studies revealed that the binding affinity for the enzyme-docked oil composition was estimated at -5.8 kcal/mol, suggesting that the combination of the substrate and lipase was stable and suitable for esterification.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11673575PMC
http://dx.doi.org/10.1021/acs.langmuir.4c02542DOI Listing

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