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Biotechnology Letters, Vol.21, No.3, 259-264, 1999
Evaluation of trichloroethylene degradation by E-coli transformed with dimethyl sulfide monooxygenase genes and/or cumene dioxygenase genes
Pseudomonas fluorescens IP01 grown on isopropylbenzene (cumene) and Acinetobacter sp. 20B grown on dimethyl sulfide (DMS) degraded up to 90% and 25% of 1.5 mg trichloroethylene (TCE)/l, respectively. Escherichia coli harboring the DMS monooxygenase genes from strain 20B, the cumene dioxygenase genes from strain IP01 and both oxygenase genes, degraded up to 50%, 75% and 88% of 75 mg TCE/l, respectively. The growth rates of the E. coli recombinants remained nearly unaffected by TCE at 15 150 mg/l. Thus, the E. coli recombinants were indicated to degrade high concentrations of TCE efficiently at least up to 150 mg l(-1).
Keywords:METHYLOSINUS-TRICHOSPORIUM OB3B;PSEUDOMONAS-PUTIDA F1;TOLUENEDIOXYGENASE;BIODEGRADATION;TOXICITY;OXIDATION;CLONING;METHANE;CHLOROFORM;BACTERIUM