Sex attractant pheromone from the rice stalk stink bug, Tibraca limbativentris Stal

被引:42
作者
Borges, Miguel
Birkett, Michael
Aldrich, Jeffrey R.
Oliver, James E.
Chiba, Mitsuo
Murata, Yasuhiro
Laumann, Raul A.
Barrigossi, Jose Alexandre
Pickett, John A.
Moraes, Maria C. B.
机构
[1] EMBRAPA, Genet Resources & Biotechnol, BR-70849970 Brasilia, DF, Brazil
[2] USDA ARS, Beltsville Agr Res Ctr, Beltsville Agr Res Ctr W, Chem Affecting Insect Behav Lab, Beltsville, MD 20705 USA
[3] Rothamsted Res, Biol Chem Div, Harpenden AL5 2JQ, Herts, England
[4] Fuji Flavor Co Ltd, Hamura City, Tokyo 2058503, Japan
[5] EMBRAPA, Rice & Beans, BR-75375000 Goiania, Go, Brazil
基金
英国生物技术与生命科学研究理事会;
关键词
semiochemical; zingiberenol; (1RS; 4RS; 1; S)-4-(1; 5; '-dimethylhex-4; '-enyl)-1-methylcyclohex-2-en-1-ol; allomone;
D O I
10.1007/s10886-006-9197-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The male-produced sex pheromone from the Brazilian rice stalk stink bug Tibraca limbativentris is reported. Olfactometer bioassays with sexually mature males and females showed that males attracted females, which suggests that males release a sex pheromone. Males were not attracted to either sex, nor were females attractive to conspecific females. Attraction of the females to males was highest at night. The headspace volatiles collected from male and female bugs were analyzed by gas chromatography (GC) and GC-mass spectrometry. Two male-specific compounds were identified as isomers of 1'S-zingiberenol, whereas a series of defensive compounds were identified in extracts from both sexes. Zingiberenol has three chiral centers, and the nonselective syntheses used produced two groups of isomers, zingiberenol I containing four isomers, namely (1RS,4RS,1'R)-4-(1',5'-dimethylhex-4'-enyl)-1-methylcyclohex-2-en-1-ol, and zingiberenol II containing the other four isomers, namely (1RS,4RS,1'S)-4-(1',5'-dimethylhex-4'-enyl)-1-methylcyclohex-2-en-1-ol. Both groups of stereoisomers were more attractive than hexane controls. The absolute configuration of the insect-produced pheromonal components remains to be elucidated, but the 1'S stereochemistry was established for at least one of the isomers.
引用
收藏
页码:2749 / 2761
页数:13
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