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. 1981 Oct;42(4):737–739. doi: 10.1128/aem.42.4.737-739.1981

Isolation and Genetic Characterization of Bacteria That Degrade Chloroaromatic Compounds

Peter A Vandenbergh 1, Ronald H Olsen 1, Joseph F Colaruotolo 2
PMCID: PMC244092  PMID: 16345872

Abstract

Bacteria were isolated from a landfill site previously used for disposal of chlorinated organic wastes. These soil isolates were capable of utilizing various chloroaromatic compounds. One such bacterial strain, designated Pseudomonas cepacia HCV (2,6-DCT) and growing on 2,6-dichlorotoluene, transferred this trait to a catechol-1,2-oxygenase mutant of Pseudomonas aeruginosa.

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Selected References

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  1. Benson S., Shapiro J. Plasmid-determined alcohol dehydrogenase activity in alkane-utilizing strains of Pseudomonas putida. J Bacteriol. 1976 May;126(2):794–798. doi: 10.1128/jb.126.2.794-798.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Chakrabarty A. M. Genetic basis of the biodegradation of salicylate in Pseudomonas. J Bacteriol. 1972 Nov;112(2):815–823. doi: 10.1128/jb.112.2.815-823.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chakrabarty A. M. Plasmids in Pseudomonas. Annu Rev Genet. 1976;10:7–30. doi: 10.1146/annurev.ge.10.120176.000255. [DOI] [PubMed] [Google Scholar]
  4. Crawford R. L., Olson P. E., Frick T. D. Catabolism of 5-chlorosalicylate by a Bacillus isolated from the Mississippi River. Appl Environ Microbiol. 1979 Sep;38(3):379–384. doi: 10.1128/aem.38.3.379-384.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dunn N. W., Gunsalus I. C. Transmissible plasmid coding early enzymes of naphthalene oxidation in Pseudomonas putida. J Bacteriol. 1973 Jun;114(3):974–979. doi: 10.1128/jb.114.3.974-979.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hansen J. B., Olsen R. H. IncP2 group of Pseudomonas, a class of uniquely large plasmids. Nature. 1978 Aug 17;274(5672):715–717. doi: 10.1038/274715a0. [DOI] [PubMed] [Google Scholar]
  7. Mercer A. A., Loutit J. S. Transformation and transfection of Pseudomonas aeruginosa: effects of metal ions. J Bacteriol. 1979 Oct;140(1):37–42. doi: 10.1128/jb.140.1.37-42.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Olsen R. H. Evolution of Pseudomonas R-plasmids: consequences of Tn1 insertion and resultant partial diploidy to chromosome and Tra- R-plasmid mobilization. J Bacteriol. 1978 Jan;133(1):210–216. doi: 10.1128/jb.133.1.210-216.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Pemberton J. M., Fisher P. R. 2,4-D plasmids and persistence. Nature. 1977 Aug 25;268(5622):732–733. doi: 10.1038/268732a0. [DOI] [PubMed] [Google Scholar]
  10. Reineke W., Knackmuss H. J. Construction of haloaromatics utilising bacteria. Nature. 1979 Feb 1;277(5695):385–386. doi: 10.1038/277385a0. [DOI] [PubMed] [Google Scholar]
  11. Rheinwald J. G., Chakrabarty A. M., Gunsalus I. C. A transmissible plasmid controlling camphor oxidation in Pseudomonas putida. Proc Natl Acad Sci U S A. 1973 Mar;70(3):885–889. doi: 10.1073/pnas.70.3.885. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Stanier R. Y., Palleroni N. J., Doudoroff M. The aerobic pseudomonads: a taxonomic study. J Gen Microbiol. 1966 May;43(2):159–271. doi: 10.1099/00221287-43-2-159. [DOI] [PubMed] [Google Scholar]
  13. Worsey M. J., Williams P. A. Metabolism of toluene and xylenes by Pseudomonas (putida (arvilla) mt-2: evidence for a new function of the TOL plasmid. J Bacteriol. 1975 Oct;124(1):7–13. doi: 10.1128/jb.124.1.7-13.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]

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