Magnetic Cross-Linked Enzyme Aggregates (mCLEAs) of Candida antarctica Lipase: An Efficient and Stable Biocatalyst for Biodiesel Synthesis


Autoria(s): Cruz Izquierdo, Álvaro; Picó, Enrique A.; López, Carmen; Serra Ferrer, Juan Luis; Llama Fontal, María Jesús
Data(s)

25/09/2015

25/09/2015

31/12/2014

Resumo

Enzyme-catalyzed production of biodiesel is the object of extensive research due to the global shortage of fossil fuels and increased environmental concerns. Herein we report the preparation and main characteristics of a novel biocatalyst consisting of Cross-Linked Enzyme Aggregates (CLEAs) of Candida antarctica lipase B (CALB) which are covalently bound to magnetic nanoparticles, and tackle its use for the synthesis of biodiesel from non-edible vegetable and waste frying oils. For this purpose, insolubilized CALB was covalently cross-linked to magnetic nanoparticles of magnetite which the surface was functionalized with –NH2 groups. The resulting biocatalyst combines the relevant catalytic properties of CLEAs (as great stability and feasibility for their reutilization) and the magnetic character, and thus the final product (mCLEAs) are superparamagnetic particles of a robust catalyst which is more stable than the free enzyme, easily recoverable from the reaction medium and reusable for new catalytic cycles. We have studied the main properties of this biocatalyst and we have assessed its utility to catalyze transesterification reactions to obtain biodiesel from non-edible vegetable oils including unrefined soybean, jatropha and cameline, as well as waste frying oil. Using 1% mCLEAs (w/w of oil) conversions near 80% were routinely obtained at 30°C after 24 h of reaction, this value rising to 92% after 72 h. Moreover, the magnetic biocatalyst can be easily recovered from the reaction mixture and reused for at least ten consecutive cycles of 24 h without apparent loss of activity. The obtained results suggest that mCLEAs prepared from CALB can become a powerful biocatalyst for application at industrial scale with better performance than those currently available.

Identificador

PLOS ONE 9 (12) : (2014) // Article ID 25551445

1932-6203

http://hdl.handle.net/10810/15686

10.1371/journal.pone.0115202

Idioma(s)

eng

Publicador

Public Library Science

Relação

http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0115202

Direitos

© 2014 Cruz-Izquierdo et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

info:eu-repo/semantics/openAccess

Palavras-Chave #iron-oxide nanoparticles #FE3O4 nanoparticles #immobilized lipase #catalyzed transesterification #enantioselective hydrolysis #covalent immobilization #potential applications #performance #CLEAs #stabilization
Tipo

info:eu-repo/semantics/article