The generation of a steroid library using filamentous fungi immobilized in calcium alginate
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[1] W. Reynolds,et al. The facile bioconversion of testosterone by alginate-immobilised filamentous fungi , 2013 .
[2] W. Reynolds,et al. Entrapment of mycelial fragments in calcium alginate: A general technique for the use of immobilized filamentous fungi in biocatalysis , 2012, Steroids.
[3] A. Lamm,et al. Steroid hydroxylation by Whetzelinia sclerotiorum, Phanerochaete chrysosporium and Mucor plumbeus , 2007, Steroids.
[4] F. Roussi,et al. The Design and Synthesis of New Steroidal Compounds as Potential Mimics of Taxoids , 2005 .
[5] A. Lamm,et al. Stemodane and stemarane diterpenoid hydroxylation by Mucor plumbeus and Whetzelinia sclerotiorum. , 2005, Phytochemistry.
[6] Atta-ur-rahman,et al. Biotransformation of (+)-androst-4-ene-3,17-dione , 2004, Natural product research.
[7] V. Nigam,et al. Continuous Production of Cephalosporin‐C by Immobilized Microbial Cells Using Symbiotic Mode in a Packed Bed Bioreactor , 2003, Artificial cells, blood substitutes, and immobilization biotechnology.
[8] P. Reese,et al. Steroid transformations with Fusarium oxysporum var. cubense and Colletotrichum musae , 1999, Steroids.
[9] J. A. Scott,et al. Defined coimmobilization of mixed microorganism cultures , 1995 .
[10] R. Azerad,et al. Microbial transformation of steroids: Contribution to 14α-hydroxylations , 1995, Steroids.
[11] R. Rogers,et al. Preparation, characterization, and antiviral activity of microbial metabolites of stemodin. , 1991, Journal of natural products.
[12] Y. Khang,et al. Enhanced β-lactam antibiotic production by coimmobilization of fungus and alga , 1988, Biotechnology Letters.
[13] B. Mattiasson,et al. Oxygen supply to immobilized cells : 1. Oxygen production by immobilized Chlorella pyrenoidosa , 1982 .
[14] K. Mosbach,et al. Formation of α-keto acids from amino acids using immobilized bacteria and algae , 1982, Biotechnology Letters.
[15] E. Chambaz,et al. Microbiological 7- and 15-hydroxylations of C-19 steroids. , 1978, Journal of steroid biochemistry.
[16] H. Tada,et al. Preparation of A-Ring conjugated enones and the corresponding alpha, beta-epoxy ketones of 17beta-acetoxy-5alpha-androstane. , 1968, The Journal of organic chemistry.
[17] H. Metz,et al. Darstellung von 7α‐Hydroxy‐ und 7α‐Methoxytestosteron‐Derivaten , 1964 .
[18] R. Dodson,et al. Microbiological Transformations. VIII. The Oxidation of Androstenedione at C-16 , 1962 .
[19] M. J. Weiss,et al. The Synthesis of Certain 7α-Alkylthio and 7α-Acylthio Steroid Hormone Derivatives , 1961 .
[20] R. Dodson,et al. Microbiological Transformations. IV. The Oxidation of Dehydroisoandrosterone at C-7 , 1959 .
[21] J. Bolte,et al. Use of biological systems for the preparation of chiral molecules. 3. Application in pheromone synthesis: preparation of sulcatol enantiomers , 1987 .
[22] A. Wettstein. Über Steroide. (24. Mitteilung). Über Δ4;6-3-Ketone der Androstan- und Pregnan-Reihe , 1940 .