| Literature DB >> 21651981 |
Bao-Jian Ding1, Marjorie A Liénard, Hong-Lei Wang, Cheng-Hua Zhao, Christer Löfstedt.
Abstract
The winter moth (Operophtera brumata L., Lepidoptera: Geometridae) utilizes a single hydrocarbon, 1,Z3,Z6,Z9-nonadecatetraene, as its sex pheromone. We tested the hypothesis that a fatty acid precursor, Z11,Z14,Z17,19-nonadecanoic acid, is biosynthesized from α-linolenic acid, through chain elongation by one 2-carbon unit, and subsequent methyl-terminus desaturation. Our results show that labeled α-linolenic acid is indeed incorporated into the pheromone component in vivo. A fatty-acyl-CoA desaturase gene that we found to be expressed in the abdominal epidermal tissue, the presumed site of biosynthesis for type II pheromones, was characterized and expressed heterologously in a yeast system. The transgenic yeast expressing this insect derived gene could convert Z11,Z14,Z17-eicosatrienoic acid into Z11,Z14,Z17,19-eicosatetraenoic acid. These results provide evidence that a terminal desaturation step is involved in the winter moth pheromone biosynthesis, prior to the decarboxylation.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21651981 DOI: 10.1016/j.ibmb.2011.05.003
Source DB: PubMed Journal: Insect Biochem Mol Biol ISSN: 0965-1748 Impact factor: 4.714