Jasmonic acid is not a biosynthetic intermediate to produce the pyrethrolone moiety in pyrethrin II
Pyrethrum ( Tanacetum cinerariifolium ) produces insecticidal compounds known as pyrethrins. Pyrethrins are esters; the acid moiety is either trans -chrysanthemic acid or pyrethric acid and the alcohol moiety of pyrethrins is either pyrethrolone, cinerolone, or jasmolone. It was generally accepted t...
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Veröffentlicht in: | Scientific reports 2020-04, Vol.10 (1), p.6366-6366, Article 6366 |
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Sprache: | eng |
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Zusammenfassung: | Pyrethrum (
Tanacetum
cinerariifolium
) produces insecticidal compounds known as pyrethrins. Pyrethrins are esters; the acid moiety is either
trans
-chrysanthemic acid or pyrethric acid and the alcohol moiety of pyrethrins is either pyrethrolone, cinerolone, or jasmolone. It was generally accepted that
cis
-jasmone was biosynthetic intermediate to produce the alcohol moieties of pyrethrin, and the biosynthetic origin of the
ci
s-jasmone was postulated to be jasmonic acid. However, there was no direct evidence to prove this hypothesis. In order to uncover the origin of pyrethrolone moiety in pyrethrin II, feeding experiments were performed employing deuterium- and
13
C-labeled compounds as substrates, and the expected labeled compounds were analyzed using UPLC MS/MS system. It was found that the pyrethrolone moiety in pyrethrin II was derived from 12-oxo-phytodienoic acid (OPDA),
iso
-OPDA and
cis
-jasmone but not from methyl jasmonate and 3-oxo-2-(2′-[
Z
]-pentenyl)-cyclopentane-1-hexanoic acid. The results supported that the biosynthesis of the pyrethrolone moiety in pyrethrin II partially used part of the jasmonic acid biosynthetic pathway, but not whole. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-020-63026-3 |