<p>Polyethylene glycol (PEG), a widely used synthetic polymer, poses significant environmental concerns due to its persistence, highlighting the need for effective degradation strategies. This study presents a novel hybrid chemo-biological system, which combines magnetic nanoparticles (Fe<sub>3</sub>O<sub>4</sub>-MNPs), hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), and recombinant (carboxylesterase/lipase) enzymes, along with magnesium (Mg<sup>2</sup>⁺) and calcium (Ca<sup>2</sup>⁺) ions as cofactors, to efficiently break down and valorize PEG. The Fe<sub>3</sub>O<sub>4</sub>-MNPs / H<sub>2</sub>O<sub>2</sub> system generates hydroxyl radicals, initiating polymer depolymerization, while enzymatic catalysis further cleaves ester bonds to produce low-molecular-weight intermediates. These intermediates are then converted into ethanol through microbial fermentation, establishing a direct pathway from PEG waste to biofuel. Optimization of the process using a central composite design (CCD) revealed synergistic effects among Fe<sub>3</sub>O<sub>4</sub>-MNPs, H<sub>2</sub>O<sub>2</sub>, and divalent ions, with moderate concentrations yielding a maximum ethanol output of 1.14%, outperforming non-optimized conditions. Our findings demonstrate a proof-of-concept platform for integrating radical chemistry with biocatalysis to degrade recalcitrant polymers and enable resource recovery. This approach provides a foundation for scalable PEG valorization and contributes to the development of sustainable polymer waste management strategies.</p><p></p>

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Single-pot nanoparticle-enzyme integration enables synergistic PEG valorization for bioethanol production

  • Anoth Maharjan,
  • Bashu Dev Pardhe,
  • Hyo Seon Kim,
  • Jungoh Ahn,
  • Jung-Ho Park

摘要

Polyethylene glycol (PEG), a widely used synthetic polymer, poses significant environmental concerns due to its persistence, highlighting the need for effective degradation strategies. This study presents a novel hybrid chemo-biological system, which combines magnetic nanoparticles (Fe3O4-MNPs), hydrogen peroxide (H2O2), and recombinant (carboxylesterase/lipase) enzymes, along with magnesium (Mg2⁺) and calcium (Ca2⁺) ions as cofactors, to efficiently break down and valorize PEG. The Fe3O4-MNPs / H2O2 system generates hydroxyl radicals, initiating polymer depolymerization, while enzymatic catalysis further cleaves ester bonds to produce low-molecular-weight intermediates. These intermediates are then converted into ethanol through microbial fermentation, establishing a direct pathway from PEG waste to biofuel. Optimization of the process using a central composite design (CCD) revealed synergistic effects among Fe3O4-MNPs, H2O2, and divalent ions, with moderate concentrations yielding a maximum ethanol output of 1.14%, outperforming non-optimized conditions. Our findings demonstrate a proof-of-concept platform for integrating radical chemistry with biocatalysis to degrade recalcitrant polymers and enable resource recovery. This approach provides a foundation for scalable PEG valorization and contributes to the development of sustainable polymer waste management strategies.