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Insights into the formation of carlactone from in-depth analysis of the CCD8-catalyzed reactions

Insights into the formation of carlactone from in-depth analysis of the CCD8-catalyzed reactions

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BRUNO, Mark, Martina VERMATHEN, Adrian ALDER, Florian WÜST, Patrick SCHAUB, Rob VAN DER STEEN, Peter BEYER, Sandro GHISLA, Salim AL-BABILI, 2017. Insights into the formation of carlactone from in-depth analysis of the CCD8-catalyzed reactions. In: FEBS Letters. 591(5), pp. 792-800. ISSN 0014-5793. eISSN 1873-3468

@article{Bruno2017-03-09Insig-39011, title={Insights into the formation of carlactone from in-depth analysis of the CCD8-catalyzed reactions}, year={2017}, doi={10.1002/1873-3468.12593}, number={5}, volume={591}, issn={0014-5793}, journal={FEBS Letters}, pages={792--800}, author={Bruno, Mark and Vermathen, Martina and Alder, Adrian and Wüst, Florian and Schaub, Patrick and van der Steen, Rob and Beyer, Peter and Ghisla, Sandro and Al-Babili, Salim} }

<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/rdf/resource/123456789/39011"> <dc:contributor>Bruno, Mark</dc:contributor> <dc:creator>Ghisla, Sandro</dc:creator> <dc:creator>van der Steen, Rob</dc:creator> <dc:creator>Vermathen, Martina</dc:creator> <dc:contributor>van der Steen, Rob</dc:contributor> <dc:contributor>Alder, Adrian</dc:contributor> <dc:contributor>Schaub, Patrick</dc:contributor> <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/39011"/> <dc:creator>Schaub, Patrick</dc:creator> <dc:contributor>Ghisla, Sandro</dc:contributor> <dcterms:abstract xml:lang="eng">Strigolactones are a new class of phytohormones synthesized from carotenoids via carlactone. The complex structure of carlactone is not easily deducible from its precursor, a cis-configured β-carotene cleavage product, and is thus formed via a poorly understood series of reactions and molecular rearrangements, all catalyzed by only one enzyme, the carotenoid cleavage dioxygenase 8 (CCD8). Moreover, the reactions leading to carlactone are expected to form a second, yet unidentified product. In this study, we used (13) C and (18) O-labeling to shed light on the reactions catalyzed by CCD8. The characterization of the resulting carlactone by LC-MS and NMR, and the identification of the assumed, less accessible second product allowed us to formulate a minimal reaction mechanism for carlactone generation.</dcterms:abstract> <dc:language>eng</dc:language> <dc:creator>Alder, Adrian</dc:creator> <dc:contributor>Vermathen, Martina</dc:contributor> <dc:creator>Wüst, Florian</dc:creator> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2017-05-23T08:41:56Z</dc:date> <dc:creator>Beyer, Peter</dc:creator> <dc:contributor>Al-Babili, Salim</dc:contributor> <dcterms:issued>2017-03-09</dcterms:issued> <dc:contributor>Beyer, Peter</dc:contributor> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2017-05-23T08:41:56Z</dcterms:available> <dc:creator>Bruno, Mark</dc:creator> <dc:creator>Al-Babili, Salim</dc:creator> <dcterms:title>Insights into the formation of carlactone from in-depth analysis of the CCD8-catalyzed reactions</dcterms:title> <dc:contributor>Wüst, Florian</dc:contributor> </rdf:Description> </rdf:RDF>

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