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Microbiology 152 (2006), 1179-1186; DOI  10.1099/mic.0.28622-0
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Microbiology 152 (2006), 1179-1186; DOI  10.1099/mic.0.28622-0
© 2006 Society for General Microbiology

The sulfonated osmolyte N-methyltaurine is dissimilated by Alcaligenes faecalis and by Paracoccus versutus with release of methylamine

Sonja Weinitschke1, Karin Denger1, Theo H. M. Smits1, Klaus Hollemeyer2 and Alasdair M. Cook1

1 Department of Biology, University of Konstanz, D-78457 Konstanz, Germany
2 Institute of Biochemical Engineering, Saarland University, Box 50 11 50, D-66041 Saarbrücken, Germany

Correspondence
Alasdair Cook
alasdair.cook{at}uni-konstanz.de

Selective enrichments yielded bacterial cultures able to utilize the osmolyte N-methyltaurine as sole source of carbon and energy or as sole source of fixed nitrogen for aerobic growth. Strain MT1, which degraded N-methyltaurine as a sole source of carbon concomitantly with growth, was identified as a strain of Alcaligenes faecalis. Stoichiometric amounts of methylamine, whose identity was confirmed by matrix-assisted, laser-desorption ionization time-of-flight mass spectrometry, and of sulfate were released during growth. Inducible N-methyltaurine dehydrogenase, sulfoacetaldehyde acetyltransferase (Xsc) and a sulfite dehydrogenase could be detected. Taurine dehydrogenase was also present and it was hypothesized that taurine dehydrogenase has a substrate range that includes N-methyltaurine. Partial sequences of a tauY-like gene (encoding the putative large component of taurine dehydrogenase) and an xsc gene were obtained by PCR with degenerate primers. Strain N-MT utilized N-methyltaurine as a sole source of fixed nitrogen for growth and could also utilize the compound as sole source of carbon. This bacterium was identified as a strain of Paracoccus versutus. This organism also expressed inducible (N-methyl)taurine dehydrogenase, Xsc and a sulfite dehydrogenase. The presence of a gene cluster with high identity to a larger cluster from Paracoccus pantotrophus NKNCYSA, which is now known to dissimilate N-methyltaurine via Xsc, allowed most of the overall pathway, including transport and excretion, to be defined. N-Methyltaurine is thus another compound whose catabolism is channelled directly through sulfoacetaldehyde.


Abbreviations: DCPIP, dichlorophenol indophenol; MALDI-TOF-MS, matrix-assisted laser-desorption ionization time-of-flight mass spectrometry

The GenBank/EMBL/DDBJ accession numbers for the partial sequences in Alcaligenes faecalis MT1 reported in this paper are: 16S rRNA gene, AM048879; putative large subunit of taurine dehydrogenase (tauY), AM048880; sulfoacetaldehyde acetyltransferase (xsc), AM048881. The sequences for Paracoccus versutus N-MT are: 16S rRNA gene, AM048882; tauCXY-xsc gene cluster, AM087667; tauZ-pta gene cluster, AM087668.




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