TY - JOUR
T1 - Male-released sex pheromone of the stink bug piezodorus hybneri
AU - Leal, Walter Soares
AU - Kuwahara, Shigefumi
AU - Shi, Xiongwei
AU - Higuchi, Hiroya
AU - Marino, Claudia E.B.
AU - Ono, Mikio
AU - Meinwald, Jerrold
PY - 1998
Y1 - 1998
N2 - Male-released semiochemicals of the stink bug Piezodorus hybneri (Heteroptera: Pentatomidae) elicit attraction of male and female bugs and homosexual behavior in males. Three active components were isolated from the airborne volatiles of males by flash chromatography, with the activity monitored by GC-EAD and behavioral bioassay. The pheromone system was characterized as a mixture of β-sesquiphellandrene, (R)-15-hexadecanolide, and methyl 8-(Z)-hexadecenoate (ratio: 10:4:1), and the activity of the semiochemicals was assessed with authentic samples. Enantiomerically pure samples of the R and S macrolactones were obtained by Yamaguchi's and Mitsunobu's macrolactonization of a key intermediate, (R)-15- hydroxyhexadecanoic acid. The nonnatural S steroisomer was neither a beneficial nor a behavioral antagonist. Individual constituents or binary mixtures were active, but the optimal male response was elicited only by the full mixture. Behavioral observation and the fact that the onset of pheromone production is coincident with ovarian development strongly suggest that these semiochemicals are, in fact, sex pheromones.
AB - Male-released semiochemicals of the stink bug Piezodorus hybneri (Heteroptera: Pentatomidae) elicit attraction of male and female bugs and homosexual behavior in males. Three active components were isolated from the airborne volatiles of males by flash chromatography, with the activity monitored by GC-EAD and behavioral bioassay. The pheromone system was characterized as a mixture of β-sesquiphellandrene, (R)-15-hexadecanolide, and methyl 8-(Z)-hexadecenoate (ratio: 10:4:1), and the activity of the semiochemicals was assessed with authentic samples. Enantiomerically pure samples of the R and S macrolactones were obtained by Yamaguchi's and Mitsunobu's macrolactonization of a key intermediate, (R)-15- hydroxyhexadecanoic acid. The nonnatural S steroisomer was neither a beneficial nor a behavioral antagonist. Individual constituents or binary mixtures were active, but the optimal male response was elicited only by the full mixture. Behavioral observation and the fact that the onset of pheromone production is coincident with ovarian development strongly suggest that these semiochemicals are, in fact, sex pheromones.
KW - Homosexual behavior, aggregation pheromone, β-sesquiphellandrene, (R)- 15-hexadecanolide, methyl 8-(Z)-hexadecenoate
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U2 - 10.1023/A:1022307600446
DO - 10.1023/A:1022307600446
M3 - Article
AN - SCOPUS:0031762470
VL - 24
SP - 1817
EP - 1829
JO - Journal of Chemical Ecology
JF - Journal of Chemical Ecology
SN - 0098-0331
IS - 11
ER -