Construction and utilization of Fe3O4@Al3 + immobilized laccase for enhancing organic diethylstilbestrol removal: A multi-spectroscopy and molecular docking investigation

As one of the endocrine-disrupting compounds (EDCs), diethylstilbestrol (DES) poses significant risks to ecosystems and human health. This study reports the development of a magnetic nanocomposite (Fe₃O₄@Al³⁺@laccase) <i>via</i> glutaraldehyde (GA) crosslinking to enhance DES degradation. The single factor experiments revealed that the optimum immobilization conditions were: temperature 40℃, pH 5, enzyme concentration 1.0 mg/mL, and immobilization time 1.0 h. Under these conditions, Fe₃O₄@Al³ ⁺@laccase achieved 91.71 %±2.95 % DES degradation within 12 h, as validated by HPLC, retaining 31.29 %±1.99 % of its initial catalytic activity after 10 reuse cycles. Notably, the immobilized laccase exhibited superior stability in organic solvents compared to free laccase. Fourier-transform infrared (FTIR) analysis confirmed that laccase was successfully conjugated onto Fe₃O₄@Al³ ⁺. Scanning electron microscopy and transmission electron microscopy revealed that the immobilization process preserved the original morphology and crystalline structure of Fe₃O₄@Al³ ⁺. Multi-spectroscopic analyses, including enzyme kinetics, fluorescence, and three-dimensional (3D) spectroscopy, elucidated the binding affinity and conformational changes between laccase and DES. Molecular docking simulations predicted a binding free energy of -6.4 kJ·mol⁻¹ , indicating that the conformation stability between laccase and surrounding free amino acids was mainly maintained <i>via</i> van der Waals, pi-pi T-shaped, Pi-Donor Hydrogen Bond, and Pi-Alkyl. This work provides proof-of-concept for using Fe₃O₄@Al³ ⁺ as a reusable magnetic support for laccase, offering a promising strategy for DES degradation and guiding the design of advanced nanomaterials for environmental bioremediation.

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Journal
Computational and Structural Biotechnology Journal
Published
2025-01-01
DOI
https://doi.org/10.1016/j.csbj.2025.07.044
Primary Topic
Enzyme-mediated dye degradation
Type
article
Field-Weighted Citation Impact
0.00

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article

Construction and utilization of Fe3O4@Al3 + immobilized laccase for enhancing organic diethylstilbestrol removal: A multi-spectroscopy and molecular docking investigation

Canfeng Bian, Tianzhu Guan, Huaxiang Li, Qingling Wang et al.
Computational and Structural Biotechnology Journal
Enzyme-mediated dye degradation
article

Construction and utilization of Fe3O4@Al3 + immobilized laccase for enhancing organic diethylstilbestrol removal: A multi-spectroscopy and molecular docking investigation

Canfeng Bian, Tianzhu Guan, Huaxiang Li, Qingling Wang, Chenxi Ren, Y P Feng
article en

Abstract

As one of the endocrine-disrupting compounds (EDCs), diethylstilbestrol (DES) poses significant risks to ecosystems and human health. This study reports the development of a magnetic nanocomposite (Fe₃O₄@Al³⁺@laccase) <i>via</i> glutaraldehyde (GA) crosslinking to enhance DES degradation. The single factor experiments revealed that the optimum immobilization conditions were: temperature 40℃, pH 5, enzyme concentration 1.0 mg/mL, and immobilization time 1.0 h. Under these conditions, Fe₃O₄@Al³ ⁺@laccase achieved 91.71 %±2.95 % DES degradation within 12 h, as validated by HPLC, retaining 31.29 %±1.99 % of its initial catalytic activity after 10 reuse cycles. Notably, the immobilized laccase exhibited superior stability in organic solvents compared to free laccase. Fourier-transform infrared (FTIR) analysis confirmed that laccase was successfully conjugated onto Fe₃O₄@Al³ ⁺. Scanning electron microscopy and transmission electron microscopy revealed that the immobilization process preserved the original morphology and crystalline structure of Fe₃O₄@Al³ ⁺. Multi-spectroscopic analyses, including enzyme kinetics, fluorescence, and three-dimensional (3D) spectroscopy, elucidated the binding affinity and conformational changes between laccase and DES. Molecular docking simulations predicted a binding free energy of -6.4 kJ·mol⁻¹ , indicating that the conformation stability between laccase and surrounding free amino acids was mainly maintained <i>via</i> van der Waals, pi-pi T-shaped, Pi-Donor Hydrogen Bond, and Pi-Alkyl. This work provides proof-of-concept for using Fe₃O₄@Al³ ⁺ as a reusable magnetic support for laccase, offering a promising strategy for DES degradation and guiding the design of advanced nanomaterials for environmental bioremediation.

Computational and Structural Biotechnology JournalVol. 29
State Key Laboratory of Food Science and Technology (CN), Yangzhou University (CN)
Government of Jiangsu Province, Natural Science Foundation of Jiangsu Province
Openalex Percentile: Top 85%
Enzyme-mediated dye degradation
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