Robust Oxidase-Mimetic Supramolecular Nanocatalyst for Lignin Biodegradation

Nano Lett. 2024 Feb 28;24(8):2520-2528. doi: 10.1021/acs.nanolett.3c04505. Epub 2024 Feb 15.

Abstract

Enzymatic catalysis presents an eco-friendly, energy-efficient method for lignin degradation. However, challenges arise due to the inherent incompatibility between enzymes and native lignin. In this work, we introduce a supramolecular catalyst composed of fluorenyl-modified amino acids and Cu2+, designed based on the aromatic stacking of the fluorenyl group, which can operate in ionic liquid environments suitable for the dissolution of native lignin. Amino acids and halide anions of ionic liquids shape the copper site's coordination sphere, showcasing remarkable catechol oxidase-mimetic activity. The catalyst exhibits thermophilic property, and maintains oxidative activity up to 75 °C, which allows the catalyzed degradation of the as-dissolved native lignin with high efficiency even without assistance of the electron mediator. In contrast, at this condition, the native copper-dependent oxidase completely lost its activity. This catalyst with superior stability and activity offer promise for sustainable lignin valorization through biocatalytic routes compatible with ionic liquid pretreatment, addressing limitations in native enzymes for industrially relevant conditions.

Keywords: Enzyme mimic; Ionic liquid; Lignin degradation; Self-assembly; Supramolecular catalyst.

MeSH terms

  • Amino Acids
  • Catalysis
  • Copper
  • Ionic Liquids* / chemistry
  • Lignin / chemistry
  • Oxidoreductases

Substances

  • Ionic Liquids
  • Lignin
  • Copper
  • Oxidoreductases
  • Amino Acids