Nanostructured materials are promising substrates for biocatalyst immobilization. We report a green and sustainable strategy for enzyme immobilization using cellulose nanocrystals (CNCs) derived from renewable sources. CNCs offer biodegradability, low toxicity, and high surface area, enabling efficient immobilization of Candida rugosa lipase (CRL). Covalent bioconjugation on TEMPO-oxidized cellulose nanocrystals (TO_CNCs) provides an almost quantitative immobilization yield without releasing toxic byproducts, but with reduced enzymatic activity per mg of immobilized protein. Conversely, nonspecific immobilization on sulfated cellulose nanocrystals (S_CNCs) shows very low immobilization yield but preserves enzyme mobility and slightly enhances activity. The immobilized biocatalysts were characterized by attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, high-resolution synchrotron X-ray diffractometry (XRD), ultraviolet-visible spectroscopy (UV-vis), field emission scanning electron microscopy (FE-SEM), bicinchoninic acid assay (BCA), solid-state nuclear magnetic resonance (ssNMR) spectroscopy, and enzymatic activity measurements. Notably, ssNMR reveals the effectiveness of TO_CNCs in preventing enzyme dispersion.

Spagnuolo, L., Lasorsa, A., D'Orsi, R., Capodieci, L., Hassan Omar, O., Micheli, L., et al. (2026). Candida rugosa Lipase Bioconjugation to Cellulose Nanocrystals with High Immobilization Efficiency: Comparison with Nonspecific Approach. BIOMACROMOLECULES, 27(2), 1612-1624 [10.1021/acs.biomac.5c02245].

Candida rugosa Lipase Bioconjugation to Cellulose Nanocrystals with High Immobilization Efficiency: Comparison with Nonspecific Approach

Micheli L.;
2026-01-01

Abstract

Nanostructured materials are promising substrates for biocatalyst immobilization. We report a green and sustainable strategy for enzyme immobilization using cellulose nanocrystals (CNCs) derived from renewable sources. CNCs offer biodegradability, low toxicity, and high surface area, enabling efficient immobilization of Candida rugosa lipase (CRL). Covalent bioconjugation on TEMPO-oxidized cellulose nanocrystals (TO_CNCs) provides an almost quantitative immobilization yield without releasing toxic byproducts, but with reduced enzymatic activity per mg of immobilized protein. Conversely, nonspecific immobilization on sulfated cellulose nanocrystals (S_CNCs) shows very low immobilization yield but preserves enzyme mobility and slightly enhances activity. The immobilized biocatalysts were characterized by attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, high-resolution synchrotron X-ray diffractometry (XRD), ultraviolet-visible spectroscopy (UV-vis), field emission scanning electron microscopy (FE-SEM), bicinchoninic acid assay (BCA), solid-state nuclear magnetic resonance (ssNMR) spectroscopy, and enzymatic activity measurements. Notably, ssNMR reveals the effectiveness of TO_CNCs in preventing enzyme dispersion.
2026
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore CHIM/01
Settore CHIM/06
Settore CHEM-01/A - Chimica analitica
Settore CHEM-05/A - Chimica organica
English
The authors would like to thank Prof. Paola Vitale for fruitful scientific discussion and Rosa Giannelli, Martina Tognoni, Maria Montrone and Erica Colaprico for preliminary experiments. Dr. Danilo Vona is acknowledged for the SDS PAGE experiment.
Spagnuolo, L., Lasorsa, A., D'Orsi, R., Capodieci, L., Hassan Omar, O., Micheli, L., et al. (2026). Candida rugosa Lipase Bioconjugation to Cellulose Nanocrystals with High Immobilization Efficiency: Comparison with Nonspecific Approach. BIOMACROMOLECULES, 27(2), 1612-1624 [10.1021/acs.biomac.5c02245].
Spagnuolo, L; Lasorsa, A; D'Orsi, R; Capodieci, L; Hassan Omar, O; Micheli, L; Van Der Wel, Pca; Operamolla, A
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/465725
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