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. Author manuscript; available in PMC: 2022 Mar 19.
Published in final edited form as: ACS Chem Biol. 2021 Feb 18;16(3):480–490. doi: 10.1021/acschembio.0c00832

Figure 7.

Figure 7.

Cartoon of the different steps of carotenoid cleavage by BCO2. The carotenoid molecule enters the substrate-binding tunnel. Cleaves at the 9,10 double bond results in the removal of one ionone ring site and the formation of an apocarotenoid. The apocarotenoid product leaves the substrate-binding cavity. The apocarotenoid then reenters the substrate-binding cavity in reverse direction followed by cleavage at the 9’,10’ double bond position. The results in the removal of the second ionone ring site and the formation of a diapocarotenoid product.