Please use this identifier to cite or link to this item: http://dx.doi.org/10.18419/opus-2000
Authors: Trenz, Stefan Peter
Strubel, Volker
Knackmuss, Hans-Joachim
Engesser, Karl-Heinrich
Title: Microbial degradation of biaryl structures: relationships between fluorene, dibenzofuran and biphenyl pathways
Issue Date: 1992
metadata.ubs.publikation.typ: Konferenzbeitrag
metadata.ubs.publikation.source: Behrens, Dieter (Hrsg.): Mikrobiologische Reinigung von Böden. Frankfurt am Main : DECHEMA, 1992. - ISBN 3-926959-29-0, S. 284-288
URI: http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-75924
http://elib.uni-stuttgart.de/handle/11682/2017
http://dx.doi.org/10.18419/opus-2000
Abstract: Initial dioxygenation of fluorene by dibenzofuran degrading strains occurs in the unusual angular position. The resulting dihydrodiendiol is converted to 3-(2-carboxyphenyl)catechol by action of a dehydrogenase. This is a novel activity for a dehydrogenase causing a C-C-bond cleavage. After growth with dibenzofuran and biphenyl respectively two different initial dioxygenases are expressed. The first enzyme shows a broad substrate range, the second enzyme only converts biphenyl. Strains degrading fluorene, dibenzofuran and biphenyl may constitute a unique physiological group.
Appears in Collections:04 Fakultät Energie-, Verfahrens- und Biotechnik

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