Nanostructured materials represent promising substrates for biocatalyst immobilization and activation. Cellulose nanocrystals (CNCs), accessible from waste and/or renewable sources, are sustainable and biodegradable, show high specific surface area for anchoring a high number of enzymatic units, and high thermal and mechanical stability. In this work, we present a holistic enzyme-based approach to functional antibacterial materials by bioconjugation between the lysozyme from chicken egg white and enzymatic cellulose nanocrystals. The neutral CNCs were prepared by endoglucanase hydrolysis from Avicel. We explore the covalent immobilization of lysozyme on enzymatic CNCs and on their TEMPO oxidized derivatives (TO-CNCs), comparing immobilization yields, material properties, and enzymatic activities. The materials were characterized by X-ray diffractometry (XRD), attenuated total reflectance Fourier Transform infrared spectroscopy (ATR-FTIR), bicinchoninic acid (BCA) assay, field-emission scanning electron microscopy (FE-SEM) and dynamic light scattering (DLS). We demonstrate the higher overall efficiency of the immobilization process carried out on TO-CNCs, based on the success of covalent bonding and on the stability of the isolated bioconjugates.TEMPO-oxidized cellulose nanocrystals (TO-CNCs) are an excellent substrate for the covalent immobilization of lysozyme from chicken egg white. The bioconjugates are synthesized, isolated and characterized and are potential candidates as antibacterial materials. image

Spagnuolo, L., Micheli, L., Dufresne, A., Beneventi, D., Operamolla, A. (2024). Covalent Lysozyme Immobilization on Enzymatic Cellulose Nanocrystals. CHEMISTRY-A EUROPEAN JOURNAL, 30(60) [10.1002/chem.202402171].

Covalent Lysozyme Immobilization on Enzymatic Cellulose Nanocrystals

Micheli L.;
2024-01-01

Abstract

Nanostructured materials represent promising substrates for biocatalyst immobilization and activation. Cellulose nanocrystals (CNCs), accessible from waste and/or renewable sources, are sustainable and biodegradable, show high specific surface area for anchoring a high number of enzymatic units, and high thermal and mechanical stability. In this work, we present a holistic enzyme-based approach to functional antibacterial materials by bioconjugation between the lysozyme from chicken egg white and enzymatic cellulose nanocrystals. The neutral CNCs were prepared by endoglucanase hydrolysis from Avicel. We explore the covalent immobilization of lysozyme on enzymatic CNCs and on their TEMPO oxidized derivatives (TO-CNCs), comparing immobilization yields, material properties, and enzymatic activities. The materials were characterized by X-ray diffractometry (XRD), attenuated total reflectance Fourier Transform infrared spectroscopy (ATR-FTIR), bicinchoninic acid (BCA) assay, field-emission scanning electron microscopy (FE-SEM) and dynamic light scattering (DLS). We demonstrate the higher overall efficiency of the immobilization process carried out on TO-CNCs, based on the success of covalent bonding and on the stability of the isolated bioconjugates.TEMPO-oxidized cellulose nanocrystals (TO-CNCs) are an excellent substrate for the covalent immobilization of lysozyme from chicken egg white. The bioconjugates are synthesized, isolated and characterized and are potential candidates as antibacterial materials. image
2024
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore CHIM/06
Settore CHIM/01
Settore CHEM-05/A - Chimica organica
Settore CHEM-01/A - Chimica analitica
English
Con Impact Factor ISI
Biocatalysis
Bioconjugation
Cellulose nanocrystals
Enzymes immobilization
Lysozyme
project “BIHO 2022-Bando Incentivi di Ateneo Horizon e Oltre”(Prot. n. 0048740/2022), MUR (Ministerodell’Università e della Ricerca) for the project PON 2014–2020(D.M. 1061/2021
Spagnuolo, L., Micheli, L., Dufresne, A., Beneventi, D., Operamolla, A. (2024). Covalent Lysozyme Immobilization on Enzymatic Cellulose Nanocrystals. CHEMISTRY-A EUROPEAN JOURNAL, 30(60) [10.1002/chem.202402171].
Spagnuolo, L; Micheli, L; Dufresne, A; Beneventi, D; Operamolla, A
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/396765
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