Literature DB >> 6940948

Formation of urso- and ursodeoxy-cholic acids from primary bile acids by Clostridium absonum.

I A Macdonald, D M Hutchison, T P Forrest.   

Abstract

Eight strains of Clostridium absonum were shown to form ursocholic acid (UC) from cholic acid (C) and ursodeoxycholic acid (UDC) from chenodeoxycholic acid (CDC) but did not transform deoxycholic acid (DC) in whole cell cultures. The structures of UC and UDC were verified by mass spectroscopy, and by thin-layer chromatography using Komarowsky's spray reagent. The organism transformed C and CDC at concentrations below 1.5. 10(-3) M and 5.0. 10(-4) M, respectively; higher concentrations were inhibitory. Optimal yields of the final products were realized at about 15-22 hr and 9-15 hr of incubation, respectively, and were in the range of 60-70%. Additionally, the 7 keto-derivatives, 7 keto-deoxycholic acid (7K-DC) or 7 keto-lithocholic acid (7K-LC) were also formed from C and CDC. With longer periods of incubation, increasing yields of 7K-DC and 7K-LC and decreasing yields of UC and UDC were observed. These time course studies suggest that 7K-DC and 7K-LC are intermediates in the formation of UC and UDC from the primary bile acids. We propose the occurrence of C right harpoon over left harpoon 7K-DC right harpoon over left harpoon UC and CDC right harpoon over left harpoon 7K-LC right harpoon over left harpoon UDC with increasing dominance of back reaction of the second step on aging of the culture. When the initial pH value of the medium was manipulated within the range of 5.8-9.0, increasing yields of UDC from CDC were obtained at higher pH values (maximum yield at pH 9.0 was 83%), with total inhibition of growth and transformation at pH 5.8. In contrast, UC was produced from C at all pH values studied, with marginal differences in yields (maximum yield at pH 8.0 was 50%). In all cases, formation of UC from C was much slower than that of UDC from CDC. In contrast, C. paraperfringens transformed none of the above bile acids. We propose that C. absonum, or a biochemically similar species, may be present in the human gut and give rise to UDC (and UC) in vivo.-Macdonald, I. A., D. M. Hutchison, and T. P. Forrest. Formation of urso- and ursodeoxycholic acids from primary acids by Clostridium absonum.

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Year:  1981        PMID: 6940948

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  11 in total

Review 1.  Ursodeoxycholic acid in the treatment of cholesterol cholelithiasis. Part II.

Authors:  W H Bachrach; A F Hofmann
Journal:  Dig Dis Sci       Date:  1982-09       Impact factor: 3.199

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

Authors:  F Aragozzini; E Canzi; A Ferrari; E Maconi; A Sidjimov
Journal:  Biochem J       Date:  1985-09-01       Impact factor: 3.857

3.  Characterization of NADP-dependent 7 beta-hydroxysteroid dehydrogenases from Peptostreptococcus productus and Eubacterium aerofaciens.

Authors:  S Hirano; N Masuda
Journal:  Appl Environ Microbiol       Date:  1982-05       Impact factor: 4.792

4.  12 beta-dehydrogenation of bile acids by Clostridium paraputrificum, C. tertium, and C. difficile and epimerization at carbon-12 of deoxycholic acid by cocultivation with 12 alpha-dehydrogenating Eubacterium lentum.

Authors:  R Edenharder; J Schneider
Journal:  Appl Environ Microbiol       Date:  1985-04       Impact factor: 4.792

Review 5.  Ursodeoxycholic acid: a review of its pharmacological properties and therapeutic efficacy.

Authors:  A Ward; R N Brogden; R C Heel; T M Speight; G S Avery
Journal:  Drugs       Date:  1984-02       Impact factor: 9.546

6.  Contribution of the 7β-hydroxysteroid dehydrogenase from Ruminococcus gnavus N53 to ursodeoxycholic acid formation in the human colon.

Authors:  Ja-Young Lee; Hisashi Arai; Yusuke Nakamura; Satoru Fukiya; Masaru Wada; Atsushi Yokota
Journal:  J Lipid Res       Date:  2013-06-01       Impact factor: 5.922

7.  Formation of ursodeoxycholic acid from chenodeoxycholic acid by a 7 beta-hydroxysteroid dehydrogenase-elaborating Eubacterium aerofaciens strain cocultured with 7 alpha-hydroxysteroid dehydrogenase-elaborating organisms.

Authors:  I A MacDonald; Y P Rochon; D M Hutchison; L V Holdeman
Journal:  Appl Environ Microbiol       Date:  1982-11       Impact factor: 4.792

8.  Clostridium scindens baiCD and baiH genes encode stereo-specific 7alpha/7beta-hydroxy-3-oxo-delta4-cholenoic acid oxidoreductases.

Authors:  Dae-Joong Kang; Jason M Ridlon; Doyle Ray Moore; Stephen Barnes; Phillip B Hylemon
Journal:  Biochim Biophys Acta       Date:  2007-11-07

9.  Dysfunction of organic anion transporting polypeptide 1a1 alters intestinal bacteria and bile acid metabolism in mice.

Authors:  Youcai Zhang; Pallavi B Limaye; Lois D Lehman-McKeeman; Curtis D Klaassen
Journal:  PLoS One       Date:  2012-04-04       Impact factor: 3.240

10.  The three-dimensional structure of Clostridium absonum 7α-hydroxysteroid dehydrogenase: new insights into the conserved arginines for NADP(H) recognition.

Authors:  Deshuai Lou; Bochu Wang; Jun Tan; Liancai Zhu; Xiaoxi Cen; Qingzhi Ji; Yue Wang
Journal:  Sci Rep       Date:  2016-03-10       Impact factor: 4.379

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