Fig. 2From: Evolution of the codling moth pheromone via an ancient gene duplicationPathway of codlemone biosynthesis. Palmitic acyl (C16) is first formed by the fatty acid synthesis pathway. Lauric acyl (C12) is then produced following two recurring reactions of beta-oxidation. A first desaturation occurs, introducing an E9 double bond between carbons 9 and 10 from the carboxyl terminus. The resulting monoenoic fatty acyl is then the substrate of a second desaturation via the removal of hydrogen atoms at the carbons 8 and 11, causing the formation of a E8E10 conjugated diene system. Finally, an unknown fatty acyl-CoA reductase converts the fatty acyl precursor into the fatty alcohol (E8,E10)-8,10-dodecadienol commonly known as codlemone. The steps characterized in this study are highlighted in redBack to article page