(6R, 10R)-6,10,14-Trimethylpentadecan-2-one, a Dominant and Behaviorally Active Component in Male Orchid Bee Fragrances

被引:20
|
作者
Eltz, Thomas [2 ]
Hedenstrom, Erik [1 ]
Bang, Joakim [1 ]
Wallin, Erika A. [1 ]
Andersson, Jimmy [1 ]
机构
[1] Mid Sweden Univ, Dept Nat Sci Engn & Math, SE-85170 Sundsvall, Sweden
[2] Univ Dusseldorf, Sensory Ecol Grp, D-40225 Dusseldorf, Germany
关键词
Hexahydrofarnesyl acetone; Hymenoptera; Euglossini; Euglossa; Pheromone; (6R, 10R)-6,10,14-trimethylpentadecan-2-one; Synthesis; Stereoisomer; DIFFERENTIATION; ACCUMULATION; COLLECTION;
D O I
10.1007/s10886-010-9873-4
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
6,10,14-Trimethylpentadecan-2-one (Hexahydrofarnesyl acetone; HHA) previously has been found to be a major component in tibial fragrances of male orchid bees, Euglossa spp. HHA is a chiral molecule with four possible stereoisomers, (6R, 10R)-, (6R, 105)-, (6S, 10R)-, and (6S, 10S)-6,10,14-trimethylpentadecan-2-one. In the present study, we characterized HHA extracted from Euglossa as the pure enantiomer (6R, 10R)-6,10,14-trimethylpentadecan-2-one. During bioassays in Mexico and Panama, the synthetic RR-isomer attracted males of six species of orchid bees, including three that were known to contain HHA in their tibial fragrances. Possible sources of HHA for wild bees are flowers of euglossophilous orchids and aroids. With a molecular weight of 268, HHA is the largest natural molecule known to attract male orchid bees in pure form, Its attractiveness to males suggests that low-volatility compounds have a function in male signals, e.g., serve as a "base note" in complex odor bouquets.
引用
收藏
页码:1322 / 1326
页数:5
相关论文
共 50 条
  • [1] (6R, 10R)-6,10,14-Trimethylpentadecan-2-one, a Dominant and Behaviorally Active Component in Male Orchid Bee Fragrances
    Thomas Eltz
    Erik Hedenström
    Joakim Bång
    Erika A. Wallin
    Jimmy Andersson
    Journal of Chemical Ecology, 2010, 36 : 1322 - 1326
  • [2] Chemoenzymatic Synthesis of (2R,6R,10R)-6,10,14-Trimethylpentadecan-2-ol, Sex Pheromone of Rice Moth (Corcyra cephalonica), and of Its (2S,6R,10R)-Diastereomer
    Shafikov, R. V.
    Spivak, A. Yu
    Odinokov, V. N.
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2011, 47 (02) : 290 - 294
  • [3] Chemoenzymatic synthesis of (2R,6R,10R)-6,10,14-trimethylpentadecan-2-ol, sex pheromone of rice moth (Corcyra cephalonica), and of its (2S,6R,10R)-diastereomer
    R. V. Shafikov
    A. Yu. Spivak
    V. N. Odinokov
    Russian Journal of Organic Chemistry, 2011, 47 : 290 - 294
  • [4] Synthesis of (2R,6R,10R)- and (2S,6R,10R)-Pristanic Acid Diastereomers
    Sugamoto, Kazuhiro
    Nishikawa, Ryoya
    Nakanishi, Tomonori
    LETTERS IN ORGANIC CHEMISTRY, 2025,
  • [5] 6,10,14-TRIMETHYLPENTADECAN-2-ONE - A BERMUDA GRASS PHAGOSTIMULANT TO FALL ARMYWORM (LEPIDOPTERA, NOCTUIDAE)
    MOHAMED, MA
    QUISENBERRY, SS
    MOELLENBECK, DJ
    JOURNAL OF CHEMICAL ECOLOGY, 1992, 18 (04) : 673 - 682
  • [6] BOUND 6,10,14-TRIMETHYLPENTADECAN-2-ONE - A USEFUL MARKER FOR PHOTODEGRADATION OF CHLOROPHYLLS WITH A PHYTOL ESTER GROUP IN SEAWATER
    RONTANI, JF
    GIRAL, PJP
    BAILLET, G
    RAPHEL, D
    ORGANIC GEOCHEMISTRY, 1992, 18 (01) : 139 - 142
  • [7] Aerobic and anaerobic metabolism of 6,10,14-trimethylpentadecan-2-one by a denitrifying bacterium isolated from marine sediments
    Rontani, JF
    Gilewicz, MJ
    Michotey, VD
    Zheng, TL
    Bonin, PC
    Bertrand, JC
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (02) : 636 - 643
  • [8] 6,10,14-TRIMETHYLPENTADECAN-2-ONE AND 6,10,14-TRIMETHYL-5-TRANS, 9-TRANS, 13-PENTADECATRIEN-2-ONE FROM ANDROGENIC GLANDS OF MALE CRAB CARCINUS-MAENAS
    FEREZOU, JP
    BERREURBONNENFANT, J
    MEUSY, JJ
    BARBIER, M
    SUCHY, M
    WIPF, HK
    EXPERIENTIA, 1977, 33 (03): : 290 - 290
  • [9] SYNTHESIS OF (-)-(6R,10R)-MATSUONE - ASSIGNMENT OF RELATIVE STEREOCHEMISTRY TO A PHEROMONE OF MATSUCOCCUS PINE BAST SCALES
    CYWIN, CL
    WEBSTER, FX
    KALLMERTEN, J
    JOURNAL OF ORGANIC CHEMISTRY, 1991, 56 (09): : 2953 - 2955
  • [10] (6R*,10R*)-Dimethyl 1,4-dioxaspiro[4.5]-decane-6,10-dicarboxylate
    Jahangiri, Amita
    Wendt, Ola F.
    Strand, Daniel
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2013, 69 : O265 - +