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Phosphotriesterase-Magnetic Nanoparticle Bioconjugates with Improved Enzyme Activity in a Biocatalytic Membrane Reactor.
Gebreyohannes, Abaynesh Yihdego; Mazzei, Rosalinda; Marei Abdelrahim, Mohamed Yahia; Vitola, Giuseppe; Porzio, Elena; Manco, Giuseppe; Barboiu, Mihail; Giorno, Lidietta.
Afiliación
  • Gebreyohannes AY; Institute on Membrane Technology , ITM-CNR, University of Calabria , via P. Bucci, 17/C , 87030 Rende , Cosenza , Italy.
  • Mazzei R; Institute on Membrane Technology , ITM-CNR, University of Calabria , via P. Bucci, 17/C , 87030 Rende , Cosenza , Italy.
  • Marei Abdelrahim MY; Institute on Membrane Technology , ITM-CNR, University of Calabria , via P. Bucci, 17/C , 87030 Rende , Cosenza , Italy.
  • Vitola G; Institut Européen des Membranes (IEM) , Université de Montpellier , Case courrier 047, 2 Place Eugène Bataillon , 34095 Montpellier cedex 5, France.
  • Porzio E; Department of Chemistry, Faculty of Science , Helwan University , Ain-Helwan, Cairo 11795 , Egypt.
  • Manco G; Institute on Membrane Technology , ITM-CNR, University of Calabria , via P. Bucci, 17/C , 87030 Rende , Cosenza , Italy.
  • Barboiu M; Institute of Protein Biochemistry , National Research Council, IBP-CNR , via P. Castellino 111 , 80131 Naples , Italy.
  • Giorno L; Institute of Protein Biochemistry , National Research Council, IBP-CNR , via P. Castellino 111 , 80131 Naples , Italy.
Bioconjug Chem ; 29(6): 2001-2008, 2018 06 20.
Article en En | MEDLINE | ID: mdl-29792416
ABSTRACT
The need to find alternative bioremediation solutions for organophosphate degradation pushed the research to develop technologies based on organophosphate degrading enzymes, such as phosphotriesterase. The use of free phosphotriesterase poses limits in terms of enzyme reuse, stability, and process development. The heterogenization of enzyme on a support and their use in bioreactors implemented by membranes seems a suitable strategy, thanks to the ability of membranes to compartmentalize, to govern mass transfer, and to provide a microenvironment with tuned physicochemical and structural properties. Usually, hydrophilic membranes are used since they easily guarantee the presence of water molecules needed for the enzyme catalytic activity. However, hydrophobic materials exhibit a larger shelf life and are preferred for the construction of filters and masks. Therefore, in this work, hydrophobic polyvinylidene fluoride (PVDF) porous membranes were used to develop biocatalytic membrane reactors (BMR). The phosphotriesterase-like lactonase (PLL) enzyme ( SsoPox triple mutant from S. solfataricus) endowed with thermostable phosphotriesterase activity was used as model biocatalyst. The enzyme was covalently bound directly to the PVDF hydrophobic membrane or it was bound to magnetic nanoparticles and then positioned on the hydrophobic membrane surface by means of an external magnetic field. Investigation of kinetic properties of the two BMRs and the influence of immobilized enzyme amount revealed that the performance of the BMR was mostly dependent on the amount of enzyme and its distribution on the immobilization support. Magnetic nanocomposite mediated immobilization showed a much better performance, with an observed specific activity higher than 90% compared to grafting of the enzyme on the membrane. Even though the present work focused on phosphotriesterase, it can be easily translated to other classes of enzymes and related applications.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Reactores Biológicos / Hidrolasas de Triéster Fosfórico / Sulfolobus solfataricus / Enzimas Inmovilizadas / Nanopartículas de Magnetita Idioma: En Revista: Bioconjug Chem Asunto de la revista: BIOQUIMICA Año: 2018 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Reactores Biológicos / Hidrolasas de Triéster Fosfórico / Sulfolobus solfataricus / Enzimas Inmovilizadas / Nanopartículas de Magnetita Idioma: En Revista: Bioconjug Chem Asunto de la revista: BIOQUIMICA Año: 2018 Tipo del documento: Article País de afiliación: Italia