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dc.contributor.authorYoshinaga, Naokoen
dc.contributor.authorIshikawa, Chihiroen
dc.contributor.authorSeidl-Adams, Irmgarden
dc.contributor.authorBosak, Elizabethen
dc.contributor.authorAboshi, Takakoen
dc.contributor.authorTumlinson, James Hen
dc.contributor.authorMori, Naokien
dc.contributor.alternative吉永, 直子ja
dc.date.accessioned2015-06-26T04:47:05Z-
dc.date.available2015-06-26T04:47:05Z-
dc.date.issued2014-05-11-
dc.identifier.issn0098-0331-
dc.identifier.urihttp://hdl.handle.net/2433/198564-
dc.description.abstractPlants attacked by insect herbivores release a blend of volatile organic compounds (VOCs) that serve as chemical cues for host location by parasitic wasps, natural enemies of the herbivores. Volicitin, N-(17-hydroxylinolenoyl)-L-glutamine, is one of the most active VOC elicitors found in herbivore regurgitants. Our previous study revealed that hydroxylation on the 17th position of the linolenic acid moiety of N-linolenoyl-L-glutamine increases by more than three times the elicitor activity in corn plants. Here, we identified N-(18-hydroxylinolenoyl)-L-glutamine (18OH-volicitin) from larval gut contents of tobacco hornworm (THW), Manduca sexta. Eggplant and tobacco, two solanaceous host plants of THW larvae, and corn, a non-host plant, responded differently to this new elicitor. Eggplant and tobacco seedlings emitted twice the amount of VOCs when 18OH-volicitin was applied to damaged leaf surfaces compared to N-linolenoyl-L-glutamine, while both these fatty acid amino acid conjugates (FACs) elicited a similar response in corn seedlings. In both solanaceous plants, there was no significant difference in the elicitor activity of 17OH- and 18OH-volicitin. Interestingly, other lepidopteran species that have 17OH-type volicitin also attack solanaceous plants. These data suggest that plants have developed herbivory-detection systems customized to their herbivorous enemies.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer USen
dc.rightsThe final publication is available at Springer via http://dx.doi.org/10.1007/s10886-014-0436-y.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.subjectVolicitinen
dc.subjectElicitoren
dc.subjectTobacco hornwormen
dc.subjectMaizeen
dc.subjectEggplanten
dc.subjectFACsen
dc.subject.meshAnimalsen
dc.subject.meshGlutamine/analogs & derivativesen
dc.subject.meshGlutamine/chemistryen
dc.subject.meshGlutamine/metabolismen
dc.subject.meshHerbivoryen
dc.subject.meshLinolenic Acids/chemistryen
dc.subject.meshLinolenic Acids/metabolismen
dc.subject.meshManduca/chemistryen
dc.subject.meshManduca/physiologyen
dc.subject.meshPlant Physiological Phenomenaen
dc.subject.meshPlants/chemistryen
dc.subject.meshSeedling/physiologyen
dc.subject.meshSolanum melongena/physiologyen
dc.subject.meshTobacco/physiologyen
dc.subject.meshVolatile Organic Compounds/analysisen
dc.subject.meshVolatile Organic Compounds/metabolismen
dc.subject.meshZea mays/physiologyen
dc.subject.meshalpha-Linolenic Acid/analogs & derivativesen
dc.subject.meshalpha-Linolenic Acid/chemistryen
dc.subject.meshalpha-Linolenic Acid/metabolismen
dc.titleN-(18-hydroxylinolenoyl)-L-glutamine: a newly discovered analog of volicitin in Manduca sexta and its elicitor activity in plants.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA00694914-
dc.identifier.jtitleJournal of chemical ecologyen
dc.identifier.volume40-
dc.identifier.issue5-
dc.identifier.spage484-
dc.identifier.epage490-
dc.relation.doi10.1007/s10886-014-0436-y-
dc.textversionauthor-
dc.startdate.bitstreamsavailable2015-05-11-
dc.identifier.pmid24817386-
dcterms.accessRightsopen access-
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