Abstract
1. Thirty-eight steroids were tested as substrates for a 7 alpha-hydroxy steroid dehydrogenase preparation from a strain of Escherichia coli; an improved method of making the crude enzyme is described. 2. Steroids having a 7 alpha-hydroxyl group in the molecule were substrates except (a) when the 5 beta-cholan-24-oic acid side chain was shortened to less than four carbon atoms and (b) in certain cases when sulphate ester groups were present in the molecule. 3. For testing with the enzyme, a new specimen of 7 alpha-hydroxy-3,12-dioxo-5 beta-cholan-24-oic acid was made, which had properties different from those previously described.
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- Anderson I. G., Haslewood G. A. Comparative studies of 'bile salts'. 20. Bile salts of the coelacanth, Latimeria chalumnae Smith. Biochem J. 1964 Oct;93(1):34–39. doi: 10.1042/bj0930034. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anderson I. G., Haslewood G. A. Comparative studies of bile salts. 5 alpha-Chimaerol, a new bile alcohol from the white sucker Catostomus commersoni Lacépède. Biochem J. 1970 Feb;116(4):581–585. doi: 10.1042/bj1160581. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anderson I. G., Haslewood G. A., Oldham R. S., Amos B., Tökés L. A more detailed study of bile salt evolution, including techniques for small-scale identification and their application to amphibian biles. Biochem J. 1974 Aug;141(2):485–494. doi: 10.1042/bj1410485. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Aries V., Hill M. J. Degradation of steroids by intestinal bacteria. II. Enzymes catalysing the oxidoreduction of the 3 alpha-, 7 alpha- and 12 alpha-hydroxyl groups in cholic acid, and the dehydroxylation of the 7-hydroxyl group. Biochim Biophys Acta. 1970 May 5;202(3):535–543. doi: 10.1016/0005-2760(70)90124-4. [DOI] [PubMed] [Google Scholar]
- BRIDGWATER R. J., BRIGGS T., HASLEWOOD G. A. Comparative studies of 'bile salts'. 14. Isolation from shark bile and partial synthesis of scymnol. Biochem J. 1962 Feb;82:285–290. doi: 10.1042/bj0820285. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Haslewood E. S., Haslewood G. A. Preparation of the 3-monosulphates of cholic acid, chenodeoxycholic acid and deoxycholic acid. Biochem J. 1976 May 1;155(2):401–404. doi: 10.1042/bj1550401. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Haslewood G. A. Bile salts of germ-free domestic fowl and pigs. Biochem J. 1971 Jun;123(1):15–18. doi: 10.1042/bj1230015. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Haslewood G. A. Metabolism of steroids: 5. Ketonic derivatives of cholic acid from cows' bile. Biochem J. 1946;40(1):52–54. doi: 10.1042/bj0400052. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Haslewood G. A., Murphy G. M., Richardson J. M. A direct enzymic assay for 7 -hydroxy bile acids and their conjugates. Clin Sci. 1973 Jan;44(1):95–98. doi: 10.1042/cs0440095. [DOI] [PubMed] [Google Scholar]
- Macdonald I. A., Williams C. N., Mahony D. E. 7Alpha-hydroxysteroid dehydrogenase from Escherichia coli B: preliminary studies. Biochim Biophys Acta. 1973 Jun 6;309(2):243–253. doi: 10.1016/0005-2744(73)90022-3. [DOI] [PubMed] [Google Scholar]