Diastereoselective Synthesis of a Lilac Aldehyde Isomer and Its Electrophysiological Detection by a Moth
Autor: | Stefan Dötterl, Karlheinz Seifert, Marc-André Schneider |
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Rok vydání: | 2013 |
Předmět: |
Male
Stereochemistry Monoterpene Bioengineering Flowers Moths Biochemistry Aldehyde Electroantennography Magnoliopsida Pollinator medicine Animals Silene latifolia Organic chemistry Molecular Biology chemistry.chemical_classification Aldehydes Olfactory receptor Behavior Animal biology lilac fungi food and beverages Stereoisomerism General Chemistry General Medicine biology.organism_classification Hadena bicruris Electrophysiological Phenomena medicine.anatomical_structure chemistry Monoterpenes Molecular Medicine Female |
Zdroj: | Chemistry & Biodiversity. 10:1252-1259 |
ISSN: | 1612-1872 |
DOI: | 10.1002/cbdv.201200385 |
Popis: | The monoterpene lilac aldehyde (=2-(5-ethenyl-5-methyloxolan-2-yl)propanal) is a widespread flower scent. Lilac aldehyde is emitted in high amounts from nocturnal plant species, and it is highly attractive to nocturnal moth pollinators, such as Hadena bicruris, the pollinating seed predator of Silene latifolia. Lilac aldehyde possesses three stereogenic centers and can occur in eight stereoisomers which induce different antennal responses in H. bicruris. The distribution pattern of stereoisomers differs among plant species, and if H. bicruris has different receptors for detecting different isomers, it may use these differences to discriminate flowers of S. latifolia hosts from flowers of non-host plants. To investigate the question whether the moths have in their antennae one olfactory receptor or several different receptors for the detection of the single lilac aldehyde isomers, (2S,2'S,5'S)-lilac aldehyde was diastereoselectively synthesized. (2S,2'S,5'S)-Lilac aldehyde and its isomeric mixture were tested electrophysiologically on antennae of H. bicruris. The results displayed antennal responses, which are characteristic for a single receptor that detects the different lilac aldehyde isomers. |
Databáze: | OpenAIRE |
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