3-(2-hydroxyphenyl)catechol as substrate for proximal meta ring cleavage in dibenzofuran degradation by Brevibacterium sp. strain DPO 1361

dc.contributor.authorStrubel, Volkerde
dc.contributor.authorEngesser, Karl-Heinrichde
dc.contributor.authorFischer, Peterde
dc.contributor.authorKnackmuss, Hans-Joachimde
dc.date.accessioned2012-08-13de
dc.date.accessioned2016-03-31T07:48:28Z
dc.date.available2012-08-13de
dc.date.available2016-03-31T07:48:28Z
dc.date.issued1991de
dc.description.abstractBrevibacterium sp. strain DPO 1361 oxygenates dibenzofuran in the unusual angular position. The 3-(2-hydroxyphenyl)catechol thus generated is subject to meta ring cleavage in the proximal position, yielding 2-hydroxy-6-(2-hydroxyphenyl)-6-oxo-2,4-hexadienoic acid, which is hydrolyzed to 2-oxo-4-pentenoate and salicylate by 2-hydroxy-6-oxo-6-phenyl-2,4-hexadienoic acid hydrolase. The proximal mode of ring cleavage is definitely established by isolation and unequivocal structural characterization of a cyclization product of 2-hydroxy-6-(2-hydroxyphenyl)-6-oxo-2,4-hexadienoic acid, i.e., 3-(chroman-4-on-2-yl)pyruvate.en
dc.identifier.other371085195de
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-76035de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/1384
dc.identifier.urihttp://dx.doi.org/10.18419/opus-1367
dc.language.isoende
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.subject.classificationMikrobieller Abbau , Brevibacterium , Biaryle , Dibenzofurande
dc.subject.ddc570de
dc.title3-(2-hydroxyphenyl)catechol as substrate for proximal meta ring cleavage in dibenzofuran degradation by Brevibacterium sp. strain DPO 1361en
dc.typearticlede
ubs.fakultaetFakultät Chemiede
ubs.fakultaetFakultät Energie-, Verfahrens- und Biotechnikde
ubs.institutInstitut für Organische Chemiede
ubs.institutInstitut für Mikrobiologiede
ubs.opusid7603de
ubs.publikation.sourceJournal of bacteriology 173 (1991), S. 1932-1937. URL http://jb.asm.org/content/173/6/1932.abstractde
ubs.publikation.typZeitschriftenartikelde

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