Isethionate formation from taurine in Chromohalobacter salexigens: purification of sulfoacetaldehyde reductase
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Amination MeSH
- Genes, Bacterial MeSH
- Bacterial Proteins genetics isolation & purification metabolism MeSH
- Chromohalobacter genetics growth & development metabolism MeSH
- Electrophoresis, Polyacrylamide Gel MeSH
- Isomerism MeSH
- Isoenzymes genetics isolation & purification metabolism MeSH
- Klebsiella oxytoca metabolism MeSH
- Isethionic Acid metabolism MeSH
- Marinomonas metabolism MeSH
- Metabolic Networks and Pathways genetics MeSH
- Multigene Family MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Taurine metabolism MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Bacterial Proteins MeSH
- Isoenzymes MeSH
- Isethionic Acid MeSH
- Taurine MeSH
Bacterial generation of isethionate (2-hydroxyethanesulfonate) from taurine (2-aminoethanesulfonate) by anaerobic gut bacteria was established in 1980. That phenomenon in pure culture was recognized as a pathway of assimilation of taurine-nitrogen. Based on the latter work, we predicted from genome-sequence data that the marine gammaproteobacterium Chromohalobacter salexigens DSM 3043 would exhibit this trait. Quantitative conversion of taurine to isethionate, identified by mass spectrometry, was confirmed, and the taurine-nitrogen was recovered as cell material. An eight-gene cluster was predicted to encode the inducible vectorial, scalar and regulatory enzymes involved, some of which were known from other taurine pathways. The genes (Csal_0153-Csal_0156) encoding a putative ATP-binding-cassette (ABC) transporter for taurine (TauAB(1)B(2)C) were shown to be inducibly transcribed by reverse transcription (RT-) PCR. An inducible taurine : 2-oxoglutarate aminotransferase [EC 2.6.1.55] was found (Csal_0158); the reaction yielded glutamate and sulfoacetaldehyde. The sulfoacetaldehyde was reduced to isethionate by NADPH-dependent sulfoacetaldehyde reductase (IsfD), a member of the short-chain alcohol dehydrogenase superfamily. The 27 kDa protein (SDS-PAGE) was identified by peptide-mass fingerprinting as the gene product of Csal_0161. The putative exporter of isethionate (IsfE) is encoded by Csal_0160; isfE was inducibly transcribed (RT-PCR). The presumed transcriptional regulator, TauR (Csal_0157), may autoregulate its own expression, typical of GntR-type regulators. Similar gene clusters were found in several marine and terrestrial gammaproteobacteria, which, in the gut canal, could be the source of not only mammalian, but also arachnid and cephalopod isethionate.
Agroscope Changins Wädenswil ACW Schloss Postfach CH 8820 Wädenswil Switzerland
Department of Biology The University D 78457 Konstanz Germany
Institute of Biochemical Engineering Saarland University Box 50 11 50 D 66041 Saarbrücken Germany
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