Abstract

Whole cells and cell extracts of Eubacterium species V. P. I. 12708 7-dehydroxylated [3H]ursodeoxycholic acid or [14C]chenodeoxycholic forming lithocholic acid. 7 beta-Dehydroxylation specific activity was 146 and 386 nmol hr-1 mg protein-1 for cell extracts and whole cells, respectively. 7 alpha- or 7 beta-Dehydroxylation activity was detected only in whole cells or cell extracts prepared from cultures grown in the presence of cholic acid. The addition of NAD+ (0.5 mM) to anaerobically dialyzed cell extracts stimulated 7 beta- and 7 alpha-dehydroxylation activity by 5- and 40-fold, respectively. The level of 7 beta-dehydroxylation specific activity was approximately 3- to 5-fold lower than 7 alpha-dehydroxylation in whole cells and 3-fold lower in cell extracts. Substrate saturation kinetics for ursodeoxycholic acid and chenodeoxycholic acid were hyperbolic and showed substrate inhibition at concentrations above 200 microM. The apparent Km values for ursodeoxycholic and chenodeoxycholic acid were 14.5 microM and 49 microM, respectively. Both 7 alpha- and 7 beta-dehydroxylase activities were inactivated (60% to 70%) by heating for 6 min at 45 degrees C. Moreover, both activities co-eluted from a anaerobic Bio-Gel A 1.5-M column as a single peak at approximately 114,000 (Mr). These data show that this intestinal anaerobic bacterium has both 7 alpha- and 7 beta-dehydroxylase activities which may be catalyzed by the same enzyme.U

Highlights

  • Whole cells and cell extracts of Eubacterium species V

  • This difference has been attributed to the decreased microbial formation and circulation of lithocholic acid in the bile of ursodeoxycholic acid-treated animals as compared to the large amounts of lithocholic acid found in chenodeoxycholicacid-treated animals

  • We have previously reported that Eubacterium sp

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Summary

Introduction

Whole cells and cell extracts of Eubacterium species V. 78-Dehydroxylation of ursodeoxycholic acid by whole cells and cell extracts of the intestinal anaerobic bacterium, Eubacterium species V. Ursodeoxycholic acid, the 76-epimer of chenodeoxycholicacid, has been reported to be efficient in the dissolution of cholesterol gallstones ( 6 ) , but does not appear to induce the hepatotoxicity seen during chenodeoxycholicacid treatment [7]. T h e epimerization is carried out by the intestinal microbial flora and is believed to proceed through a 7-ketolithocholic acid intermediate In this regard, Macdonald, Hutchison, and Forrest [12] recently reported that pure cultures of Clostridium absonum could epimerize chenodeoxycholicacid to ursodeoxycholic acid and the biotransformation proceeded through a 7-ketolithocholic acid intermediate.

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