Synthesis of Novel Polymer-Assisted Organic-Inorganic Hybrid Nanoflowers and Their Application in Cascade Biocatalysis.

GOx/HRP enzyme cascade enzyme kinetics hybrid nanoflowers polyamide microparticles polymer-assisted biocatalysts synchrotron WAXS/SAXS

Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
14 Jan 2023
Historique:
received: 28 10 2022
revised: 04 01 2023
accepted: 10 01 2023
entrez: 21 1 2023
pubmed: 22 1 2023
medline: 25 1 2023
Statut: epublish

Résumé

This study reports on the synthesis of novel bienzyme polymer-assisted nanoflower complexes (PANF), their morphological and structural characterization, and their effectiveness as cascade biocatalysts. First, highly porous polyamide 6 microparticles (PA6 MP) are synthesized by activated anionic polymerization in solution. Second, the PA6 MP are used as carriers for hybrid bienzyme assemblies comprising glucose oxidase (GOx) and horseradish peroxidase (HRP). Thus, four PANF complexes with different co-localization and compartmentalization of the two enzymes are prepared. In samples NF GH/PA and NF GH@PA, both enzymes are localized within the same hybrid flowerlike organic-inorganic nanostructures (NF), the difference being in the way the PA6 MP are assembled with NF. In samples NF G/PAiH and NF G@PAiH, only GOx is located in the NF, while HRP is preliminary immobilized on PA6 MP. The morphology and the structure of the four PANF complexes have been studied by microscopy, spectroscopy, and synchrotron X-ray techniques. The catalytic activity of the four PANF was assessed by a two-step cascade reaction of glucose oxidation. The PANF complexes are up to 2-3 times more active than the free GOx/HRP dyad. They also display enhanced kinetic parameters, superior thermal stability in the 40-60 °C range, optimum performance at pH 4-6, and excellent storage stability. All PANF complexes are active for up to 6 consecutive operational cycles.

Identifiants

pubmed: 36677897
pii: molecules28020839
doi: 10.3390/molecules28020839
pmc: PMC9864776
pii:
doi:

Substances chimiques

Glucose Oxidase EC 1.1.3.4
Horseradish Peroxidase EC 1.11.1.-
Enzymes, Immobilized 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Fundação para a Ciência e Tecnologia
ID : UID/CTM/50025/2019
Organisme : ALBA Synchrotron (Spain)
ID : Project ID 2018/022726
Organisme : Fundação para a Ciência e Tecnologia
ID : Personal program contract CTTI-51/18-IPC
Organisme : Fundação para a Ciência e Tecnologia
ID : PhD grant FCT UI/BD/150854/2021

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Auteurs

Joana F Braz (JF)

IPC-Institute for Polymers and Composites, University of Minho, 4800-056 Guimarães, Portugal.

Nadya V Dencheva (NV)

IPC-Institute for Polymers and Composites, University of Minho, 4800-056 Guimarães, Portugal.

Marc Malfois (M)

ALBA Synchrotron Facility, Cerdanyola del Valés, 0890 Barcelona, Spain.

Zlatan Z Denchev (ZZ)

IPC-Institute for Polymers and Composites, University of Minho, 4800-056 Guimarães, Portugal.

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Classifications MeSH