Summary
A culture of Actinomyces albus 3006 is incapable of reducing the 20-keto group of 17α,21-deoxy-Δ4-3-keto steroids except when the substrate contains an oxygen function in the 11-position.
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Leonid M. Kogan, I. V. Ulezlo, G. K. Skryabin, N. N. Suvorov, and I. V. Torgov, Izv. AN SSSR, Otd. khim. n.,1963, 328.
F. Lindner, R. Junk, G. Nesemann, and J. Schmidt-Thome, Z. physiol. Chem.,313, 117 (1958).
M. Welsh and C. Heusghem, Compt. rend. Soc. Biol.,142, 1074 (1948).
B. J. Magerlein and R. H. Levin, J. Am. Chem. Soc.,75, 3654 (1953).
L. F. Fieser and M. Fieser, Steroids (New York, 1959), p. 612.
J. K. Noryrnberski and G. F. Woods, J. Chem. Soc.,1955, 3426.
E. A. Mistryukov, Coll. Czechosl. chem. Comm.,26, 2071 (1961).
L. Cerny, J. Joska, and L. Labler, Coll. Czechosl. chem. Comm.,26, 1658 (1961).
L. Starka, and J. Malikova, J. Endocrinol.22, 215 (1961).
D. H. Peterson and H. C. Murray, J. Am. Chem. Soc.,74, 1852 (1952).
H. L. Herzog, M. J. Gentles, H. Marchall, and E. B. Hershberg, J. Am. Chem. Soc.,83, 4073 (1961).
K. Heusler, J. Kalvoda, P. Wieland, and A. Wettstein, Helv. chim. Acta,44, 179 (1961).
J. M. Constantin, A. C. Haven, and L. H. Sarett, J. Am. Chem. Soc.,75, 1716 (1953).
R. Neher and A. Wettstein, Helv. chim. Acta,43, 1189 (1960).
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We are deeply grateful to Dr. M. Shirasaka (Japan), Dr. P. Djassi (USA), and Dr. B. Camerino (Italy) for kindly providing samples of 7β-hydroxyprogesterone, 15α-hydroxyprogesterone, and 15β-hydroxyprogesterone.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya No. 11, pp. 2008–2015, November, 1964
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Kogan, L.M., Ulezlo, I.V., Kozlova, I.K. et al. Microbiological transformations of steroids. Russ Chem Bull 13, 1908–1913 (1964). https://doi.org/10.1007/BF00844486
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DOI: https://doi.org/10.1007/BF00844486