Trichloroethylene degradation by Escherichia coli containing the cloned Pseudomonas putida F1 toluene dioxygenase genes

Appl Environ Microbiol. 1989 Dec;55(12):3162-6. doi: 10.1128/aem.55.12.3162-3166.1989.

Abstract

Toluene dioxygenase from Pseudomonas putida F1 has been implicated as an enzyme capable of degrading trichloroethylene. This has now been confirmed with Escherichia coli JM109(pDTG601) that contains the structural genes (todC1C2BA) of toluene dioxygenase under the control of the tac promoter. The extent of trichloroethylene degradation by the recombinant organism depended on the cell concentration and the concentration of trichloroethylene. A linear rate of trichloroethylene degradation was observed with the E. coli recombinant strain. In contrast, P. putida F39/D, a mutant strain of P. putida F1 that does not contain cis-toluene dihydrodiol dehydrogenase, showed a much faster initial rate of trichloroethylene degradation which decreased over time.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Biodegradation, Environmental
  • Chemical Phenomena
  • Chemistry
  • Chromatography, Gas
  • Cloning, Molecular
  • Escherichia coli / enzymology*
  • Escherichia coli / genetics
  • Oxidation-Reduction
  • Oxygenases / genetics*
  • Oxygenases / metabolism
  • Pseudomonas / enzymology*
  • Pseudomonas / genetics
  • Trichloroethylene / metabolism*

Substances

  • Trichloroethylene
  • Oxygenases
  • toluene dioxygenase