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dc.contributor.authorOhno, Shoen
dc.contributor.authorYokota, Mizukien
dc.contributor.authorYamada, Harukaen
dc.contributor.authorTatsuzawa, Fumien
dc.contributor.authorDoi, Motoakien
dc.contributor.alternative大野, 翔ja
dc.contributor.alternative横田, 瑞季ja
dc.contributor.alternative山田, 晴香ja
dc.contributor.alternative土井, 元章ja
dc.date.accessioned2022-02-22T09:42:00Z-
dc.date.available2022-02-22T09:42:00Z-
dc.date.issued2021-
dc.identifier.urihttp://hdl.handle.net/2433/268024-
dc.description.abstractYellow color in dahlia flowers is conferred from chalcones, butein and isoliquiritigenin. The color intensity of yellow dahlia cultivars is diverse, but a detailed study on this has not yet been performed. In this study, we first identified structures of flavonoids by nuclear magnetic resonance imaging in ray florets of the red-white bicolor ‘Shukuhai’, which contains chalcones, flavones and anthocyanins. Four anthocyanins, four flavone derivatives, five isoliquiritigenin derivatives and five butein derivatives were identified. Among the identified compounds, butein 4'-malonylsophoroside is considered to be the final product for butein derivatives and the presence of chalcone 4'-glucosyltransferase, chalcone 4'-glucoside glucosyltransferase, and chalcone 4'-glucoside malonyltransferase for isoliquiritigenin and butein modification was predicted. Also, the biosynthetic pathway of butein and isoliquiritigenin derivatives in dahlia with butein 4'-malonylsophoroside as the final product was predicted from the identified compounds. Next, we used nine yellow cultivars and lines with different color intensities and analyzed the correlation between the b* value, an indicator of yellow color, and level of chalcones. There was no difference in the presence or absence of major peaks among the cultivars and lines. Peak area per fresh weight measured by HPLC was high in butein 4'-malonylglucoside, butein 4'-sophoroside and isoliquiritigenin 4'-malonylglucoside, suggesting these three compounds were accumulated abundantly. Among the identified chalcones, the highest correlation coefficient was detected between the b* value and butein 4'-malonylglucoside (r = 0.86), butein 4'-sophoroside (r = 0.82) or isoliquiritigenin 4'-malonylglucoside (r = 0.76). These results suggest that these three chalcones confer yellow color in dahlia ray florets. The findings in this study will contribute not only to efforts at breeding new yellow dahlia cultivars, but also to molecular breeding of yellow flowers in other species by introducing the butein biosynthetic pathway.en
dc.language.isoeng-
dc.publisherJapanese Society for Horticultural Scienceen
dc.publisher.alternative園芸学会ja
dc.rights© 2021 The Japanese Society for Horticultural Science (JSHS), All rights reserved.en
dc.rights発行元の許可を得て登録しています.ja
dc.subjectbuteinen
dc.subjectflavonoiden
dc.subjectflower coloren
dc.subjectisoliquiritigeninen
dc.subjectNMRen
dc.titleIdentification of Chalcones and their Contribution to Yellow Coloration in Dahlia (Dahlia variabilis) Ray Floretsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleThe Horticulture Journalen
dc.identifier.volume90-
dc.identifier.issue4-
dc.identifier.spage450-
dc.identifier.epage459-
dc.relation.doi10.2503/hortj.utd-305-
dc.textversionpublisher-
dc.relation.NAID130008107330-
dcterms.accessRightsopen access-
datacite.awardNumber 18K14455-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-18K14455/-
dc.identifier.pissn2189-0102-
dc.identifier.eissn2189-0110-
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitle鮮黄色フラボノイドであるブテイン生合成機構の解明ja
出現コレクション:学術雑誌掲載論文等

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