Repression of phenol catabolism by organic acids in Ralstonia eutropha

Appl Environ Microbiol. 1998 Jan;64(1):1-6. doi: 10.1128/AEM.64.1.1-6.1998.

Abstract

During batch growth of Ralstonia eutropha (previously named Alcaligenes eutrophus) on phenol in the presence of acetate, acetate was found to be the preferred substrate; this organic acid was rapidly metabolized, and the specific rate of phenol consumption was considerably decreased, although phenol consumption was not abolished. This decrease corresponded to a drop in phenol hydroxylase and catechol-2,3-dioxygenase specific activities, and the synthesis of the latter was repressed at the transcriptional level. Studies with a mutant not able to consume acetate indicated that the organic acid itself triggers the repression. Other organic acids were also found to repress phenol degradation. One of these, benzoate, was found to completely block the catabolism of phenol (diauxic growth). A mutant unable to metabolize benzoate was also unable to develop on benzoate-phenol mixtures, indicating that the organic acid rather than a metabolite involved in benzoate degradation was responsible for the repression observed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / metabolism
  • Alcaligenes / enzymology
  • Alcaligenes / genetics
  • Alcaligenes / metabolism*
  • Benzoates / metabolism
  • Benzoic Acid
  • Catechol 2,3-Dioxygenase
  • DNA Transposable Elements
  • Dioxygenases*
  • Enzyme Repression
  • Kinetics
  • Mixed Function Oxygenases / biosynthesis
  • Mixed Function Oxygenases / metabolism
  • Mutagenesis, Insertional
  • Oxygenases / biosynthesis
  • Oxygenases / metabolism
  • Phenols / metabolism*
  • Plasmids
  • Transcription, Genetic

Substances

  • Acetates
  • Benzoates
  • DNA Transposable Elements
  • Phenols
  • Benzoic Acid
  • Mixed Function Oxygenases
  • Oxygenases
  • Dioxygenases
  • Catechol 2,3-Dioxygenase
  • phenol 2-monooxygenase