Purification and characterization of a 1,2-dihydroxynaphthalene dioxygenase from a bacterium that degrades naphthalenesulfonic acids

J Bacteriol. 1991 Jun;173(12):3795-802. doi: 10.1128/jb.173.12.3795-3802.1991.

Abstract

1,2-Dihydroxynaphthalene dioxygenase was purified to homogeneity from a bacterium that degrades naphthalenesulfonic acids (strain BN6). The enzyme requires Fe2+ for maximal activity and consists of eight identical subunits with a molecular weight of about 33,000. Analysis of the NH2-terminal amino acid sequence revealed a high degree of homology (22 of 29 amino acids) with the NH2-terminal amino acid sequence of 2,3-dihydroxybiphenyl dioxygenase from strain Pseudomonas paucimobilis Q1. 1,2-Dihydroxynaphthalene dioxygenase from strain BN6 shows a wide substrate specificity and also cleaves 5-, 6-, and 7-hydroxy-1,2-dihydroxynaphthalene, 2,3- and 3,4-dihydroxybiphenyl, catechol, and 3-methyl- and 4-methylcatechol. Similar activities against the hydroxy-1,2-dihydroxynaphthalenes were also found in cell extracts from naphthalene-degrading bacteria.

MeSH terms

  • Amino Acid Sequence
  • Bacteria / enzymology*
  • Bacteria / genetics
  • Biodegradation, Environmental
  • Dioxygenases*
  • Enzyme Induction
  • Genes, Bacterial
  • Molecular Sequence Data
  • Molecular Weight
  • Naphthalenesulfonates / metabolism*
  • Oxidation-Reduction
  • Oxygenases / biosynthesis
  • Oxygenases / genetics
  • Oxygenases / isolation & purification*
  • Oxygenases / metabolism
  • Pseudomonas / enzymology
  • Pseudomonas / genetics
  • Sequence Homology, Nucleic Acid
  • Spectrophotometry, Ultraviolet
  • Substrate Specificity

Substances

  • Naphthalenesulfonates
  • Oxygenases
  • dihydroxynaphthalene oxygenase
  • Dioxygenases
  • 2,3-dihydroxybiphenyl oxygenase