Frydman R B, Bari S, Tomaro M L, Frydman B
Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Argentina.
Biochem Biophys Res Commun. 1990 Aug 31;171(1):465-73. doi: 10.1016/0006-291x(90)91416-p.
The substrate specificity of rat liver biliverdin reductase was probed using helical and extended biliverdins. The former were the ZZZ-all-syn biliverdins IX alpha and IX gamma, and the latter were the 5Z-syn, 10Z-syn, 15Z-anti; 5Z-anti, 10E-anti, 15E-anti biliverdins. It was found that the reduction rates of the biliverdins increased with the progressive stretching of their conformations. The most extended biliverdin was reduced at a higher rate than biliverdin IX alpha. The chemical reduction rates to bilirubins followed a similar pattern. Nucleophilic addition of 2-mercaptoethanol to the C10 methine was also favored in the extended biliverdins.