Microbial Hydroxylation of Progesterone with Phomopsis Sp.

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Abstract:

Microbial hydroxylation of progesterone occurred in the biotransformation by Phomopsis sp.. The conversion products were purified by column chromatography with ether/EtOAc and characterized by spectroscopic methods including 1HNMR, 13C NMR, IR, UV and MS. Those conversion products were identified as 11α-hydroxyprogesterone (2), 11α,15β-dihydroxy progesterone (3),11α-dihydroxypreg-1,4-dien-3,20-dione (4), 6β,15βdihydroxypregesterone (5) and 7β,15βdihydroxypregesterone (6).

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Advanced Materials Research (Volumes 781-784)

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1168-1171

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September 2013

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© 2013 Trans Tech Publications Ltd. All Rights Reserved

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[1] D. H. Peterson and H. C. Murray, Journal of the American Chemical Society Vol. 74 (1952), p.1871.

Google Scholar

[2] M. Shibahara, J. A. Moody and L. L. Smith, Biochimica et biophysica acta Vol. 202 (1970), p.172.

Google Scholar

[3] S. H. Hu, X. F. Tian, Y. H. Sun and G. D. Han, Steroids Vol. 61 (1996), p.407.

Google Scholar

[4] M. L. Choudhary, I. Batool, S. A. A. Shah, S. A. Nawaz and R. Atta Ur, Chemical & Pharmaceutical Bulletin Vol. 53 (2005), p.1455.

DOI: 10.1248/cpb.53.1455

Google Scholar

[5] L. Tan and L. L. Smith, Biochim Biophys Acta Vol. 152 (1968), p.758.

Google Scholar

[6] K. Yildirim, Collection of Czechoslovak Chemical Communications Vol. 75 (2010), p.1273.

Google Scholar

[7] R. V. Smith and J. P. Rosazza, Archives of Biochemistry and Biophysics Vol. 161 (1974), p.551.

Google Scholar

[8] A. Li and J. C. Bigelow, Steroids Vol. 75 (2010), p.404.

Google Scholar

[9] M. Yoshihama, M. Nakakoshi, K. Tamura, N. Miyata, G. Kawanishi and M. Iida, Journal of Fermentation and Bioengineering Vol. 67 (1989), p.238.

DOI: 10.1016/0922-338x(89)90225-0

Google Scholar

[10] J. Schneide, Journal of Steroid Biochemistry and Molecular Biology Vol. 5 (1974), p.9.

Google Scholar

[11] S. Sun, M. Y. Kim, T. Chaisan, Y. W. Lee, K. Van and S. H. Lee, J. Phytopathol. Vol. 161 (2013), p.131.

Google Scholar

[12] Q. Wu, Y. Guo, Z. K. Guo, Y. L. Chu, T. Wang and R. X. Tan, Chemistry of Natural Compounds Vol. 48 (2013), p.938.

Google Scholar

[13] K. E. Smith, S. Latif and D. N. Kirk, J Steroid Biochem Vol. 32 (1989), p.445.

Google Scholar

[14] D. N. Kirk, B. W. Miller, S. A. Latif and D. J. Morris, Journal of Chemical Research-S Vol. 6(1989), p.164.

Google Scholar

[15] M. I. Choudhary, I. Batool, S. A. Shah, S. A. Nawaz and R. Atta ur, Chem Pharm Bull (Tokyo) Vol. 53 (2005), p.1455.

DOI: 10.1248/cpb.53.1455

Google Scholar

[16] I.C. Muhammad, N Muhammad, N.K. Shamsun, A Muhammad, A.A. Rahat, Syed M. Khalil, Atta-ur-Rahman, Z Naturforsch Vol. 62b (2007), p.593.

Google Scholar

[17] A. Y. Reeder and G. E. Joannou, Steroids Vol. 61 (1996), p.74.

Google Scholar