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.
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Two supplementary figures are available with the online version of this paper.
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Edited by: W. Bitter
- Abbreviations:
- C23O
- catechol-2,3-dioxygenase
- TDO
- toluene dioxygenase
- 6-vinyl HODA
- 2-hydroxy-6-vinylhexa-2,4-dienoate