A study on the mechanism of the epimerization at C-3 of chenodeoxycholic acid by Clostridium perfringens.

The mechanism of 3-hydroxy epimerization of chenodeoxycholic acid by Clostridium perfringens was investigated in 3 alpha, 7 alpha-dihydroxy-2,2,4,4-2H4]-, 3 alpha, 7 alpha-dihydroxy-3 beta-2H]- and 3 beta, 7 alpha-dihydroxy-3 alpha-2H]-5 beta-cholanoic acid transformations. Our findings rule out a dehydration-rehydration pathway and agree with a redox mechanism involving 3-oxochenodeoxycholic acid as intermediate.