Complete nucleotide sequence and evolutionary significance of a chromosomally encoded naphthalene-degradation lower pathway from Pseudomonas stutzeri AN10

Gene. 2000 Mar 7;245(1):65-74. doi: 10.1016/s0378-1119(00)00038-x.

Abstract

Pseudomonas stutzeri strain AN10 is a naphthalene-degrading strain whose dissimilatory genes are chromosomally encoded. We sequenced the entire naphthalene-degradation lower pathway of P. stutzeri AN10, this being, together with the upper-pathway reported previously (Bosch R. et al., 1999a. Gene 236, 149-157) the first complete DNA sequence for an entire naphthalene-catabolic pathway. Eleven open reading frames were identified. The nahGTHINLOMKJ genes encode enzymes for the metabolism of salicylate to pyruvate and acetyl-CoA, and nahR encodes the NahR regulatory protein. Our findings suggest that catabolic modules were recruited through transposition events and recombination among tnpA-like genes, and subsequent rearrangements and deletions of non-essential DNA fragments allowed the formation of the actual catabolic pathway. Our results also suggest that the genes encoding the xylene/toluene-degradation enzymes of P. putida mt-2 (pWW0) have coexisted with the nah genes of the P. stutzeri AN10 ancestral genome. This could allow the selection, via recombination events among homologous genes, for a combination of genes enabling the metabolism of a given aromatic compound in the ancestral host strain. Such events accelerate the evolution of modern catabolic pathways and provide new genetic material to the environment, ultimately resulting in improved, natural, bioremediation potential.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacterial Proteins / genetics
  • Base Sequence
  • Chromosome Mapping
  • Chromosomes, Bacterial / genetics*
  • Cloning, Molecular
  • DNA, Bacterial / chemistry
  • DNA, Bacterial / genetics*
  • Evolution, Molecular*
  • Gene Expression Regulation, Bacterial
  • Molecular Sequence Data
  • Naphthalenes / metabolism*
  • Operon / genetics
  • Promoter Regions, Genetic
  • Pseudomonas / genetics*
  • Pseudomonas / metabolism
  • Salicylates / metabolism
  • Sequence Analysis, DNA
  • Transcription Factors / genetics

Substances

  • Bacterial Proteins
  • DNA, Bacterial
  • NahR protein, Bacteria
  • Naphthalenes
  • Salicylates
  • Transcription Factors
  • naphthalene

Associated data

  • GENBANK/AF039534