Environmental And Evolutionary Microbiology

Less is more: reduced catechol production permits Pseudomonas putida F1 to grow on styrene

  • 1Field of Environmental Toxicology, Cornell University, Ithaca, NY 14850, USA
  • 2Department of Microbiology, Cornell University, Ithaca, NY 14850, USA
  • Correspondence
    Anthony Hay agh5{at}cornell.edu
  • Microbiology 2012; 158(Pt 11):2781–2788 · https://doi.org/10.1099/mic.0.058230-0

    View at publisher PubMed

    Abstract

    Pseudomonas putida F1 is unable to grow on styrene due to the accumulation of 3-vinylcatechol, a toxic metabolite that is produced through the toluene degradation (tod) pathway and causes catechol-2,3-dioxygenase (C23O) inactivation. In this study, we characterized a spontaneous F1 mutant, designated SF1, which acquired the ability to grow on styrene and did not accumulate 3-vinylcatechol. Whereas adaptation to new aromatic substrates has typically been shown to involve increased C23O activity or the acquisition of resistance to C23O inactivation, SF1 retained wild-type C23O activity. Surprisingly, SF1 grew more slowly on toluene, its native substrate, and exhibited reduced toluene dioxygenase (TDO) activity (approximately 50 % of that of F1), the enzyme responsible for ring hydroxylation and subsequent production of 3-vinylcatechol. DNA sequence analysis of the tod operon of SF1 revealed a single base pair mutation in todA (C479T), a gene encoding the reductase component of TDO. Replacement of the wild-type todA allele in F1 with todAC479T reduced TDO activity to SF1 levels, obviated vinylcatechol accumulation, and conferred the ability to grow on styrene. This novel ‘less is more’ strategy – reduced catechol production as a means to expand growth substrate range – sheds light on an alternative approach for managing catechol toxicity during the metabolism of aromatic compounds.

    • Two supplementary figures are available with the online version of this paper.

    • Edited by: W. Bitter

    Abbreviations:
    C23O
    catechol-2,3-dioxygenase
    TDO
    toluene dioxygenase
    6-vinyl HODA
    2-hydroxy-6-vinylhexa-2,4-dienoate