Metabolism of 2,6-dimethylnaphthalene by flavobacteria

Author:

Barnsley E A1

Affiliation:

1. Department of Biochemistry, Memorial University of Newfoundland, St. John's, Canada.

Abstract

Flavobacteria that were able to grow on 2,6-dimethylnaphthalene (2,6-DMN) were isolated from soil. Most were able to oxidize a broad range of aromatic hydrocarbons after growth on 2,6-DMN at rates comparable to that of the oxidation of 2,6-DMN itself. One small group was neither able to grow on naphthalene nor able to oxidize this compound after growth on 2,6-DMN, but metabolized 2,6-DMN by a pathway which converged with that previously described for naphthalene metabolism in pseudomonads. These organisms could also grow on salicylate or methylsalicylate, and in so doing, early enzymes for 2,6-DMN metabolism were induced.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference29 articles.

1. Substituent effects in naphthalene. I. The synthesis of 4,5,6,7 and 8-substituted 2- naphthoic acids;Adcock W.;Aust. J. Chem.,1965

2. The induction of the enzymes of naphthalene metabolism in pseudomonads by salicylate and 2-aminobenzoate;Barnsley E. A.;J. Gen. Microbiol.,1975

3. Naphthalene metabolism of pseudomonads: the oxidation of 1,2-dihydroxynaphthalene to 2-hydroxychromene-2-carboxylic acid and the formation of 2'-hydroxybenzalpyruvate;Barnsley E. A.;Biochem. Biophys. Res. Commun.,1976

4. Bacterial oxidation of naphthalene and phenanthrene;Barnsley E. A.;J. Bacteriol.,1983

5. Bayly R. C. and M. G. Barbour. 1984. The degradation of aromatic compounds by the meta and gentisate pathways p. 253-294. In D. T. Gibson (ed.) Microbial degradation of organic compounds. Marcel Dekker Inc. New York.

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