Literature DB >> 28004294

Identification, Synthesis, and Field Tests of the Sex Pheromone of Margarodes prieskaensis (Jakubski).

Barend V Burger1, C André de Klerk2, Michael Morr3, Wilhelmina J G Burger4.   

Abstract

Here, we report the identification and synthesis of the sex pheromone of female Margarodes prieskaensis (Jakubski), and the attractiveness of the synthetic pheromone to males in field trapping tests. Volatile organic compounds were collected from virgin females using a sample enrichment probe (SEP). Analyses by gas chromatography coupled to mass spectrometry revealed the presence of only two constituents. By scaling up the SEP, sufficient of the major constituent was collected for 1H and 13C nuclear magnetic resonance (NMR) analyses and ancillary NMR techniques. The sex attractant was identified as (2R,4R,6R,8R)-2,4,6,8-tetramethylundecan-1-ol. The enantiomerically pure compound was synthesized from octadecyl (2R,4R,6R,8R)-2,4,6,8-tetramethylundecanoate, a minor component of the uropygial (preen) gland secretion of the domestic goose, Anser domesticus. Field trapping experiments, carried out in vineyards in the Northern Cape Province of South Africa, showed that the synthetic compound was as attractive to winged males of M. prieskaensis as virgin females. The second compound detected was identified as the corresponding acetate, but addition of this did not affect the attractiveness of the major component. We believe this to be the first identification of a sex attractant of the Margarodidae.

Entities:  

Keywords:  (2R,4R,6R,8R)-2,4,6,8-tetramethylundecan-1-ol; Bioassay; Headspace analysis; Hemiptera; Margarodes prieskaensis; Margarodidae; SEP; Sample enrichment probe; Sex pheromone; Sternorrhyncha

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Year:  2016        PMID: 28004294     DOI: 10.1007/s10886-016-0801-0

Source DB:  PubMed          Journal:  J Chem Ecol        ISSN: 0098-0331            Impact factor:   2.626


  10 in total

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Journal:  Hoppe Seylers Z Physiol Chem       Date:  1952

2.  Direct assignment of the relative configuration in 1,3,n-methyl-branched carbon chains by (1)H NMR spectroscopy.

Authors:  Yvonne Schmidt; Bernhard Breit
Journal:  Org Lett       Date:  2010-05-21       Impact factor: 6.005

3.  Enantioselective total synthesis and determination of the absolute configuration of the 4,6,8,10,16,18-hexamethyldocosane from Antitrogus parvulus.

Authors:  Christian Herber; Bernhard Breit
Journal:  Angew Chem Int Ed Engl       Date:  2005-08-19       Impact factor: 15.336

4.  Simplified analysis of organic compounds in headspace and aqueous samples by high-capacity sample enrichment probe.

Authors:  Ben V Burger; Brenda Marx; Maritha le Roux; Wina J G Burger
Journal:  J Chromatogr A       Date:  2006-05-11       Impact factor: 4.759

5.  Controlled-release pheromone dispenser for use in traps to monitor flight activity of false codling moth.

Authors:  J H Hofmeyr; B V Burger
Journal:  J Chem Ecol       Date:  1995-03       Impact factor: 2.626

Review 6.  Chiral methyl-branched pheromones.

Authors:  Tetsu Ando; Rei Yamakawa
Journal:  Nat Prod Rep       Date:  2015-07       Impact factor: 13.423

7.  Novel cuticular hydrocarbons from the cane beetle Antitrogus parvulus--4,6,8,10,16-penta- and 4,6,8,10,16,18-hexamethyldocosanes-unprecedented anti-anti-anti-stereochemistry in the 4,6,8,10-methyltetrad.

Authors:  Sharon Chow; Mary T Fletcher; Lynette K Lambert; Oliver P Gallagher; Christopher J Moore; Bronwen W Cribb; Peter G Allsopp; William Kitching
Journal:  J Org Chem       Date:  2005-03-04       Impact factor: 4.354

8.  Assignment of relative configuration of desoxypropionates by 1H NMR spectroscopy: method development, proof of principle by asymmetric total synthesis of xylarinic acid A and applications.

Authors:  Yvonne Schmidt; Konrad Lehr; Lucie Colas; Bernhard Breit
Journal:  Chemistry       Date:  2012-04-27       Impact factor: 5.236

9.  Development of second-generation sample enrichment probe for improved sorptive analysis of volatile organic compounds.

Authors:  B V Burger; M le Roux; B Marx; S A Herbert; K T Amakali
Journal:  J Chromatogr A       Date:  2011-01-20       Impact factor: 4.759

10.  Mammalian exocrine secretions. XVIII: Chemical characterization of interdigital secretion of red hartebeest, Alcelaphus buselaphus caama.

Authors:  B Reiter; B V Burger; J Dry
Journal:  J Chem Ecol       Date:  2003-10       Impact factor: 2.626

  10 in total

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