Biocatalytic oxidation of phenolic compounds by bovine methemoglobin in the presence of H2O2: quantitative structure-activity relationships

J Hazard Mater. 2012 Nov 30:241-242:207-15. doi: 10.1016/j.jhazmat.2012.09.028. Epub 2012 Sep 23.

Abstract

In the present work, 13 p-substituted phenols with different functional groups have been systematically evaluated as metHb substrates by means of HPLC analysis. Non-hyperbolic kinetics were observed and Hill coefficients in the 0.37-1.00 range were obtained. The catalytic constants and the Hill coefficients were found to be quantitatively correlated with two independent variables: the energy level of the highest-occupied molecular orbital (E(HOMO)), which describes the intrinsic redox activity of the substrates and the pK(a)-values, which are related to substrate ionization. Oxygen evolution in the presence of each phenol derivative was also measured, and good correlation between peroxidase-like and catalase-like activities of the protein was observed. It is also shown that bovine metHb, although less active than other peroxidases, may represent a good alternative from an economical point of view for phenol removal processes. The equations here obtained may serve as a basis to further explore the potential use of metHb-mediated reactions in the treatment of phenols in wastewaters and to predict which phenol will be removed most efficiently under this treatment with satisfactory reliability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biocatalysis
  • Cattle
  • Hydrogen Peroxide / chemistry*
  • Kinetics
  • Methemoglobin / chemistry*
  • Oxidation-Reduction
  • Phenols / chemistry
  • Phenols / isolation & purification*
  • Quantitative Structure-Activity Relationship
  • Wastewater / analysis*
  • Water Pollutants, Chemical / chemistry
  • Water Pollutants, Chemical / isolation & purification*
  • Water Purification / methods*

Substances

  • Phenols
  • Waste Water
  • Water Pollutants, Chemical
  • Methemoglobin
  • Hydrogen Peroxide