Bio-based and cost effective method for phenolic compounds removal using cross-linked enzyme aggregates

J Hazard Mater. 2021 Feb 5:403:124021. doi: 10.1016/j.jhazmat.2020.124021. Epub 2020 Sep 17.

Abstract

This work aimed at presenting a green method using a new source of peroxidase isolated from Raphanus sativus var. niger (RSVNP) in immobilized form, for the treatment of wastewater. To ensure stability and enzymatic activity in the biodegradation process, RSVNP was immobilized as a cross-linked enzyme aggregate (CLEAs). With more than 29% of recovered activity and 85% aggregation yield, acetone was selected as the best precipitating agent. The formed protein aggregates required 2% (v/v) of glutaraldehyde (GA) concentration and a ratio of 9:1 (v/v) enzyme (E) amount to cross-linker (E/GA). Compared to the free enzyme, RSVNP-CLEAs were found more chemically and thermally stable and exhibited good storage stability for more than 8 weeks. In addition, RSVNP-CLEAs were evaluated for their ability to remove phenol and p-cresol from aqueous solution by varying several operating conditions. A maximal yield (98%) of p-cresol conversion was recorded after 40 min; while 92% of phenol was degraded after 1 h duration time. The reusability of RSVNP-CLEAs was tested, displaying 71% degradation of phenol in the third batch carried out and more than 54% was achieved for p-cresol after four successive reuses in the presence of hydrogen peroxide at 2 mM concentration.

Keywords: CLEAs; Enzymatic transformation; Green process; Peroxidase immobilization; Phenols.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cost-Benefit Analysis
  • Cross-Linking Reagents
  • Enzyme Stability
  • Enzymes, Immobilized* / metabolism
  • Glutaral
  • Hydrogen-Ion Concentration
  • Phenols*
  • Temperature

Substances

  • Cross-Linking Reagents
  • Enzymes, Immobilized
  • Phenols
  • Glutaral