TY - JOUR
T1 - Novel Floral Scent Compounds from Night-Blooming Araceae Pollinated by Cyclocephaline Scarabs (Melolonthidae, Cyclocephalini)
AU - Maia, Artur Campos D.
AU - Grimm, Christopher
AU - Schubert, Mario
AU - Etl, Florian
AU - Gonçalves, Eduardo Gomes
AU - Do Amaral Ferraz Navarro, Daniela Maria
AU - Schulz, Stefan
AU - Dötterl, Stefan
N1 - Publisher Copyright:
© 2018, The Author(s).
PY - 2019/2
Y1 - 2019/2
N2 - Nocturnal flowering plants often release strong scents to attract their pollinators. Among night active flower visitors are cyclocephaline scarab beetles, which have been demonstrated to respond to uncommon volatile organic compounds released in high amounts by their host plants. In Araceae, the molecular structure of several such compounds is yet to be unveiled. We investigated headspace floral scent samples of Philodendron squamiferum, Thaumatophyllum mello-baretoanum, and Xanthosoma hylaeae by a variety of approaches, leading to the identification of novel compounds. Dehydrojasmone, (Z)-4-methylene-5-(pent-2-en-1-yl)cyclopent-2-en-1-one (1), (Z)-3-methylene-2-(pent-2-en-1-yl)cyclopentyl acetate (isojasmyl acetate, 3), and (E)-4,8-dimethylnona-1,3,7-trien-5-yl acetate (4) had not been previously reported, while full analytical data of the recently described (Z)-3-methylene-2-(pent-2-en-1-yl)cyclopentan-1-ol (isojasmol, 2) are presented here. All these compounds are derived from more common precursors, (Z)-jasmone and (E)-4,8-dimethyl-1,3,7-nonatriene, likely through biosynthetic “post-processing”.
AB - Nocturnal flowering plants often release strong scents to attract their pollinators. Among night active flower visitors are cyclocephaline scarab beetles, which have been demonstrated to respond to uncommon volatile organic compounds released in high amounts by their host plants. In Araceae, the molecular structure of several such compounds is yet to be unveiled. We investigated headspace floral scent samples of Philodendron squamiferum, Thaumatophyllum mello-baretoanum, and Xanthosoma hylaeae by a variety of approaches, leading to the identification of novel compounds. Dehydrojasmone, (Z)-4-methylene-5-(pent-2-en-1-yl)cyclopent-2-en-1-one (1), (Z)-3-methylene-2-(pent-2-en-1-yl)cyclopentyl acetate (isojasmyl acetate, 3), and (E)-4,8-dimethylnona-1,3,7-trien-5-yl acetate (4) had not been previously reported, while full analytical data of the recently described (Z)-3-methylene-2-(pent-2-en-1-yl)cyclopentan-1-ol (isojasmol, 2) are presented here. All these compounds are derived from more common precursors, (Z)-jasmone and (E)-4,8-dimethyl-1,3,7-nonatriene, likely through biosynthetic “post-processing”.
KW - ATTRACTIVENESS
KW - Attractants
KW - BEETLE POLLINATION
KW - BIOSYNTHESIS
KW - Beetle pollination
KW - CHEMISTRY
KW - CIS-JASMONE
KW - ECOLOGY
KW - EVOLUTION
KW - Floral scents
KW - High resolution mass spectrometry
KW - NMR spectroscopy
KW - Preparative gas chromatography
KW - Volatile organic compounds
UR - http://www.scopus.com/inward/record.url?scp=85053693704&partnerID=8YFLogxK
U2 - 10.1007/s10886-018-1018-1
DO - 10.1007/s10886-018-1018-1
M3 - Article
SN - 1573-1561
VL - 45
SP - 204
EP - 213
JO - Journal of Chemical Ecology
JF - Journal of Chemical Ecology
IS - 2
ER -