{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T14:09:14Z","timestamp":1790863754773,"version":"4.1.0"},"reference-count":56,"publisher":"Oxford University Press (OUP)","issue":"1","license":[{"start":{"date-parts":[[2001,1,1]],"date-time":"2001-01-01T00:00:00Z","timestamp":978307200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2001,1,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Alamethicin (ALA), a voltage-gated, ion channel-forming peptide mixture from Trichoderma viride, is a potent elicitor of the biosynthesis of volatile compounds in lima bean (Phaseolus lunatus). Unlike elicitation with jasmonic acid or herbivore damage, the blend of substances emitted comprises only the two homoterpenes, 4,11-dimethylnona-1,3,7-triene and 4,8,12-trimethyltrideca-1,3,7,11-tetraene, and methyl salicylate. Inhibition of octadecanoid signaling by aristolochic acid and phenidone as well as mass spectrometric analysis of endogenous jasmonate demonstrate that ALA induces the biosynthesis of volatile compounds principally via the octadecanoid-signaling pathway (20-fold increase of jasmonic acid). ALA also up-regulates salicylate biosynthesis, and the time course of the production of endogenous salicylate correlates well with the appearance of the methyl ester in the gas phase. The massive up-regulation of the SA-pathway (90-fold) interferes with steps in the biosynthetic pathway downstream of 12-oxophytodienoic acid and thereby reduces the pattern of emitted volatiles to compounds previously shown to be induced by early octadecanoids. ALA also induces tendril coiling in various species like Pisum, Lathyrus, and Bryonia, but the response appears to be independent from octadecanoid biosynthesis, because inhibitors of lipoxygenase and phospholipase A2 do not prevent the coiling reaction.<\/jats:p>","DOI":"10.1104\/pp.125.1.369","type":"journal-article","created":{"date-parts":[[2002,7,27]],"date-time":"2002-07-27T04:59:39Z","timestamp":1027745979000},"page":"369-377","source":"Crossref","is-referenced-by-count":206,"title":["Ion Channel-Forming Alamethicin Is a Potent Elicitor of Volatile Biosynthesis and Tendril Coiling. Cross Talk between Jasmonate and Salicylate Signaling in Lima Bean"],"prefix":"10.1093","volume":"125","author":[{"given":"Ju\u0308rgen","family":"Engelberth","sequence":"first","affiliation":[{"name":"Max Planck Institute for Chemical Ecology, Carl-Zeiss-Promenade 10, D\u201307745 Jena, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thomas","family":"Koch","sequence":"additional","affiliation":[{"name":"Max Planck Institute for Chemical Ecology, Carl-Zeiss-Promenade 10, D\u201307745 Jena, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Go\u0308de","family":"Schu\u0308ler","sequence":"additional","affiliation":[{"name":"Max Planck Institute for Chemical Ecology, Carl-Zeiss-Promenade 10, D\u201307745 Jena, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nadine","family":"Bachmann","sequence":"additional","affiliation":[{"name":"Max Planck Institute for Chemical Ecology, Carl-Zeiss-Promenade 10, D\u201307745 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