7alpha- and 12alpha-Hydroxysteroid dehydrogenases from Acinetobacter calcoaceticus lwoffii: a new integrated chemo-enzymatic route to ursodeoxycholic acid

Steroids. 2008 Dec 22;73(14):1385-90. doi: 10.1016/j.steroids.2008.06.013. Epub 2008 Jul 12.

Abstract

We report the very efficient biotransformation of cholic acid to 7-keto- and 7,12-diketocholic acids with Acinetobacter calcoaceticus lwoffii. The enzymes responsible of the biotransformation (i.e. 7alpha- and 12alpha-hydroxysteroid dehydrogenases) are partially purified and employed in a new chemo-enzymatic synthesis of ursodeoxycholic acid starting from cholic acid. The first step is the 12alpha-HSDH-mediated total oxidation of sodium cholate followed by the Wolf-Kishner reduction of the carbonyl group to chenodeoxycholic acid. This acid is then quantitatively oxidized with 7alpha-HSDH to 7-ketochenodeoxycholic acid, that was chemically reduced to ursodeoxycholic acid (70% overall yield).

MeSH terms

  • Acinetobacter calcoaceticus / enzymology*
  • Biotransformation
  • Catalysis
  • Cells, Cultured
  • Cholic Acids / metabolism
  • Hydroxysteroid Dehydrogenases / isolation & purification
  • Hydroxysteroid Dehydrogenases / metabolism*
  • Ursodeoxycholic Acid / metabolism*

Substances

  • Cholic Acids
  • Ursodeoxycholic Acid
  • Hydroxysteroid Dehydrogenases
  • 7 alpha-hydroxysteroid dehydrogenase
  • 12 alpha-hydroxysteroid dehydrogenase