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

G. J. Zylstra, L. P. Wackett, D. T. Gibson

Research output: Contribution to journalArticlepeer-review

86 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)3162-3166
Number of pages5
JournalApplied and environmental microbiology
Volume55
Issue number12
DOIs
StatePublished - 1989

Fingerprint

Dive into the research topics of 'Trichloroethylene degradation by Escherichia coli containing the cloned Pseudomonas putida F1 toluene dioxygenase genes'. Together they form a unique fingerprint.

Cite this