Please use this identifier to cite or link to this item: http://dx.doi.org/10.18419/opus-2008
Authors: Engesser, Karl-Heinrich
Rubio, Miguel Angel
Knackmuss, Hans-Joachim
Title: Bacterial metabolism of side-chain-fluorinated aromatics: unproductive meta-cleavage of 3-trifluoromethylcatechol
Issue Date: 1990
metadata.ubs.publikation.typ: Zeitschriftenartikel
metadata.ubs.publikation.source: Applied microbiology and biotechnology 32 (1990), S. 600-608. URL http://dx.doi.org./10.1007/BF00173734
URI: http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-76440
http://elib.uni-stuttgart.de/handle/11682/2025
http://dx.doi.org/10.18419/opus-2008
Abstract: Sixteen bacterial strains capable of degrading alkylbenzenes and alkylphenols were directly isolated from soil and water. The degradation pathways are discussed. Alkylcatechols are almost exclusively cleaved via meta-ring fission. Meta-cleavage of 3-trifluoromethyl-(TFM)-catechol was observed with all strains at different rates although the reaction rates compared to catechol as a substrate varied considerably. All 2-hydroxy-6-oxohepta-2,4-dienoic acid hydrolases investigated showed strong binding of 7,7,7-trifluoro-2-hydroxy-6-oxohepta-2,4-dienoic acid, the ring fission product of 3-TFM-catechol. Turnover rates, however, were negligible indicating this compound to be a general dead-end metabolite during metabolism of TFM-substituted compounds via meta-cleavage pathways.
Appears in Collections:04 Fakultät Energie-, Verfahrens- und Biotechnik

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