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j.phytochem.2014.04.019.pdf2.86 MBAdobe PDF見る/開く
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dc.contributor.authorSato-Masumoto, Naokoen
dc.contributor.authorIto, Michihoen
dc.contributor.alternative佐藤(増本) , 直子ja
dc.contributor.alternative伊藤, 美千穂ja
dc.date.accessioned2014-06-06T02:13:55Z-
dc.date.available2014-06-06T02:13:55Z-
dc.date.issued2014-08-
dc.identifier.issn0031-9422-
dc.identifier.urihttp://hdl.handle.net/2433/187787-
dc.description.abstractStudies on the biosynthesis of oil compounds in Perilla will help in understanding regulatory systems of secondary metabolites and in elucidating reaction mechanisms for natural product synthesis. In this study, two types of alcohol dehydrogenases, an aldo-keto reductase (AKR) and a geraniol dehydrogenase (GeDH), which are thought to participate in the biosynthesis of perilla essential oil components, such as citral and perillaldehyde, were isolated from three pure lines of perilla. These enzymes shared high amino acid sequence identity within the genus Perilla, and were expressed regardless of oil type. The overall reaction from geranyl diphosphate to citral was performed in vitro using geraniol synthase and GeDH to form a large proportion of citral and relatively little geraniol as reaction products. The biosynthetic pathway from geranyl diphosphate to citral, the main compound of citral-type perilla essential oil, was established in this study.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier Ltd.en
dc.rights© 2014 Elsevier Ltd.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.rightsThis is not the published version. Please cite only the published version.en
dc.subjectPerillaen
dc.subjectLabiataeen
dc.subjectAldo–keto reductaseen
dc.subjectGeraniol dehydrogenaseen
dc.subjectGeraniolen
dc.subjectCitralen
dc.subjectSequential enzymatic reactionen
dc.subjectBiosynthetic pathwayen
dc.subjectEssential oilen
dc.titleTwo types of alcohol dehydrogenase from Perilla can form citral and perillaldehyde.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA00774558-
dc.identifier.jtitlePhytochemistryen
dc.identifier.volume104-
dc.identifier.spage12-
dc.identifier.epage20-
dc.relation.doi10.1016/j.phytochem.2014.04.019-
dc.textversionauthor-
dc.identifier.pmid24864017-
dcterms.accessRightsopen access-
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