“…In ripe tomatoes, the cytosolic enzymes LeCCD1A and LeCCD1B perform an oxidative cleavage of multiple linear carotenoids, either at the 5,6, 7,8, or 9,10 positions, and cyclic carotenoids at the 9,10 position. This leads to the biosynthesis of dialdehydes and ketones, forming several C13 volatiles such as pseudoionone, β-ionone, 6-methyl-5-hepten-2-one, β-damascenone and geranylacetone, which is reported to be generated by the oxidative cleavage of phytoene, phytofluene, ζ-carotene, and neurosporene [18,26,[47][48][49]. In tomatoes, the LeCCD1 cleavage of lycopene at the 5,6 position leads to 6-methyl-5-hepten-2-one, which is associated with the tomato-like flavour and sweet floral aroma of tomatoes [48,50].…”