Transformation of some 3α-substituted steroids by Aspergillus tamarii KITA reveals stereochemical restriction of steroid binding orientation in the minor hydroxylation pathway
暂无分享,去创建一个
[1] Alina Świzdor,et al. Studies on Baeyer–Villiger oxidation of steroids: DHEA and pregnenolone d-lactonization pathways in Penicillium camemberti AM83 , 2009, Steroids.
[2] C. Dedi,et al. An unusual ring—A opening and other reactions in steroid transformation by the thermophilic fungus Myceliophthora thermophila , 2009, The Journal of Steroid Biochemistry and Molecular Biology.
[3] G. Carrea,et al. Enzymatic Baeyer-Villiger oxidation of steroids with cyclopentadecanone monooxygenase , 2009 .
[4] A. C. Hunter,et al. Transformation of 5-ene steroids by the fungus Aspergillus tamarii KITA: mixed molecular fate in lactonization and hydroxylation pathways with identification of a putative 3beta-hydroxy-steroid dehydrogenase/Delta5-Delta4 isomerase pathway. , 2009, Biochimica et biophysica acta.
[5] Alina Świzdor,et al. Baeyer-Villiger oxidation of DHEA, pregnenolone, and androstenedione by Penicillium lilacinum AM111 , 2008, Steroids.
[6] Atta-ur-rahman,et al. Microbial transformation of testosterone by Rhizopus stolonifer and Fusarium lini , 2008, Natural Product Research.
[7] A. A. Zohri,et al. Progesterone side-chain degradation by some species ofAspergillus flavus group , 2008, Folia Microbiologica.
[8] A. C. Hunter,et al. Distinct metabolic handling of 3beta-hydroxy-17a-oxa-D-homo-5alpha-androstan-17-one by the filamentous fungus Aspergillus tamarii KITA: Evidence in support of steroid/hydroxylase binding hypothesis. , 2007, Biochimica et biophysica acta.
[9] Hong-min Liu,et al. Synthesis of steroidal lactone by penicillium citreo-viride , 2006, Steroids.
[10] A. C. Hunter,et al. Ring-B functionalized androst-4-en-3-ones and ring-C substituted pregn-4-en-3-ones undergo differential transformation in Aspergillus tamarii KITA: ring-A transformation with all C-6 substituted steroids and ring-D transformation with C-11 substituents. , 2006, Biochimica et biophysica acta.
[11] M. Donova,et al. Steroid 17β-reduction by microorganisms—a review , 2005 .
[12] A. C. Hunter,et al. Fate of novel Quasi reverse steroidal substrates by Aspergillus tamarii KITA: bypass of lactonisation and an exclusive role for the minor hydroxylation pathway. , 2005, Biochimica et biophysica acta.
[13] J. Dmochowska‐Gladysz,et al. Steroids’ transformations in Penicillium notatum culture , 2005, Steroids.
[14] M. Faramarzi,et al. Microbial production of testosterone and testololactone in the culture of Aspergillus terreus , 2004 .
[15] A. Hunter,et al. Flexibility of the endogenous progesterone lactonisation pathway in Aspergillus tamarii KITA: transformation of a series of cortical steroid analogues , 2003, The Journal of Steroid Biochemistry and Molecular Biology.
[16] J. R. Hanson,et al. The hydroxylation of steroidal ring D lactones by Cephalosporium aphidicola. , 1998 .
[17] A. M. Khallil,et al. Microbiological transformation of progesterone by some zoosporic fungi , 1996 .
[18] H. Holland. Models for the regiochemistry and stereochemistry of microbial hydroxylation and sulfoxidation , 1994 .
[19] K. A. White,et al. A survey of the high-field 1H NMR spectra of the steroid hormones, their hydroxylated derivatives, and related compounds , 1990 .
[20] H. Holland. The mechanism of the microbial hydroxylation of steroids , 1982 .
[21] J. Blunt,et al. 13C n.m.r. spectra of steroids —a survey and commentary† , 1977 .
[22] R. McCrindle,et al. Microbiological hydroxylation of 17-norkauran-16-one and ent-17-norkauran-16-one with the fungus Rhizopus nigricans , 1975 .
[23] E. R. Jones. The microbiological hydroxylation of steroids and related compounds , 1973, Pure and applied chemistry. Chimie pure et appliquee.
[24] F. W. Parrish,et al. Microbial transformation of a series of androgens with Aspergillus tamarii. , 1967, The Journal of organic chemistry.
[25] A. Oehlschlager,et al. TRANSFORMATION OF PROGESTERONE AND RELATED STEROIDS BY ASPERGILLUS TAMARII. , 1965, Journal of Organic Chemistry.