Affiliation:
1. Insect Chemical Ecology Laboratory, USDA, Agricultural Research Service, Beltsville, MD, 20705 USA
Abstract
Experiments were conducted using tritiated European corn borer, Ostrinia nubilalis (Hübner), pheromone, (Z)-[11,12-3H2]-11-tetradecen-1-ol acetate, a tritiated fluorinated analog of the European corn borer pheromone, 2-fluoro-(Z)-[11,12-3H2]-11-tetradecen-1-ol acetate, and methyl-4-bromocrotonate (MBC) to determine if pheromone catabolism proceeds on the moth's antennae via the β-oxidation pathway of fatty acid degradation. When antennae were treated with tritiated natural pheromone plus MBC (a precursor of the known β-oxidation inhibitor, 4-bromocrotonic acid), catabolism of the pheromone was significantly inhibited. When the 2-fluoro pheromone analog was applied alone to antennae, it was hydrolyzed to the corresponding alcohol but was not degraded. MBC had no effect on catabolism of the 2-fluoro analog, and 2-fluoro substitution inhibited entrance of the compound into β-oxidation. These results demonstrate that β-oxidation is the primary oxidative pathway by which pheromone is degraded on the antennae of European corn borer moths.
Publisher
Georgia Entomological Society
Subject
Insect Science,Agronomy and Crop Science,Ecology, Evolution, Behavior and Systematics
Cited by
3 articles.
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1. Molecular Basis of Pheromone Detection in Insects ☆;Reference Module in Life Sciences;2017
2. Molecular Basis of Pheromone Detection in Insects;Comprehensive Molecular Insect Science;2005
3. Biochemical diversity of odor detection;Insect Pheromone Biochemistry and Molecular Biology;2003