Trenz, Stefan PeterStrubel, VolkerKnackmuss, Hans-JoachimEngesser, Karl-Heinrich2012-08-132016-03-312012-08-132016-03-311992370896475http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-75924http://elib.uni-stuttgart.de/handle/11682/2017http://dx.doi.org/10.18419/opus-2000Initial 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.eninfo:eu-repo/semantics/openAccessMikrobieller Abbau , Biaryle570Microbial degradation of biaryl structures: relationships between fluorene, dibenzofuran and biphenyl pathwaysconferenceObject2012-08-15