Publikation: Isethionate as a product from taurine during nitrogen-limited growth of Klebsiella oxytoca TauN1
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Klebsiella oxytoca TauN1 represents a group of isolates which utilise taurine (2-aminoethanesulfonate) quantitatively as a sole source of combined nitrogen for aerobic growth. During growth, a compound is excreted, which has now been identified as isethionate (2-hydroxyethanesulfonate). An ion-chromatographic separation of isethionate was developed to quantify the putative isethionate, whose identity was confirmed by matrix-assisted, laser-desorption ionisation time-of-flight mass spectrometry. Strain TauN1 utilised taurine (and excreted isethionate) concomitantly with growth. Cell-free extracts contained inducible taurine transaminase, which yielded sulfoacetaldehyde. A soluble, NADP-dependent isethionate dehydrogenase converted sulfoacetaldehyde to isethionate. The enzyme was partially purified and it apparently belonged to the family of short-chain alcohol dehydrogenases.
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STYP REKOWSKI, Katharina, Karin DENGER, Alasdair M. COOK, 2005. Isethionate as a product from taurine during nitrogen-limited growth of Klebsiella oxytoca TauN1. In: Archives of Microbiology. 2005, 183(5), pp. 325-330. ISSN 0302-8933. eISSN 1432-072X. Available under: doi: 10.1007/s00203-005-0776-7BibTex
@article{StypRekowski2005Iseth-7226,
year={2005},
doi={10.1007/s00203-005-0776-7},
title={Isethionate as a product from taurine during nitrogen-limited growth of Klebsiella oxytoca TauN1},
number={5},
volume={183},
issn={0302-8933},
journal={Archives of Microbiology},
pages={325--330},
author={Styp Rekowski, Katharina and Denger, Karin and Cook, Alasdair M.}
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<dcterms:abstract xml:lang="eng">Klebsiella oxytoca TauN1 represents a group of isolates which utilise taurine (2-aminoethanesulfonate) quantitatively as a sole source of combined nitrogen for aerobic growth. During growth, a compound is excreted, which has now been identified as isethionate (2-hydroxyethanesulfonate). An ion-chromatographic separation of isethionate was developed to quantify the putative isethionate, whose identity was confirmed by matrix-assisted, laser-desorption ionisation time-of-flight mass spectrometry. Strain TauN1 utilised taurine (and excreted isethionate) concomitantly with growth. Cell-free extracts contained inducible taurine transaminase, which yielded sulfoacetaldehyde. A soluble, NADP-dependent isethionate dehydrogenase converted sulfoacetaldehyde to isethionate. The enzyme was partially purified and it apparently belonged to the family of short-chain alcohol dehydrogenases.</dcterms:abstract>
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<dcterms:bibliographicCitation>First publ. in: Archives of Microbiology 183 (2005), 5, pp. 325-330</dcterms:bibliographicCitation>
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