Cloning, expression and characterization of catechol 1,2-dioxygenase from Burkholderia cepacia

J Gen Appl Microbiol. 2020 Aug 26;66(3):188-194. doi: 10.2323/jgam.2019.06.002. Epub 2019 Nov 12.

Abstract

The present study reports on the cloning, expression and characterization of catechol 1,2-dioxygenase (CAT) of bacterial strains isolated from dioxin-contaminated soils in Vietnam. Two isolated bacterial strains DF2 and DF4 were identified as Burkholderia cepacia based on their 16S rRNA sequences. Their genes coding CAT was amplified with a specific pair of primers. Recombinant CAT (rCAT) was expressed in E. coli M15 cells and its activity was confirmed by the detection of cis,cis-muconic acid, a product from catechol, by high-performance liquid chromatography (HPLC) analysis. The rCAT of DF4 had an optimal pH and temperature of 7 and 30°C, respectively. Metal ions, such as Zn2+ and Mn2+, and surfactants, such as SDS, Tween 20 and Triton X100, strongly inhibited enzyme activity, while K+ slightly increased the activity.

Keywords: Burkholderia cepacia; cat gene; catechol 1,2-dioxygenase; dibenzofuran.

MeSH terms

  • Burkholderia cepacia / enzymology*
  • Burkholderia cepacia / genetics
  • Catechol 1,2-Dioxygenase / antagonists & inhibitors
  • Catechol 1,2-Dioxygenase / chemistry
  • Catechol 1,2-Dioxygenase / genetics*
  • Catechol 1,2-Dioxygenase / metabolism*
  • Catechols / metabolism
  • Cloning, Molecular
  • Dioxins / analysis
  • Genes, Bacterial
  • Hydrogen-Ion Concentration
  • Metals / pharmacology
  • Soil Microbiology
  • Soil Pollutants / analysis
  • Surface-Active Agents / pharmacology
  • Temperature

Substances

  • Catechols
  • Dioxins
  • Metals
  • Soil Pollutants
  • Surface-Active Agents
  • Catechol 1,2-Dioxygenase