Optimization of the Method of Obtaining 9α-Hydroxy-androst-4-ene-3,17-dione—the Key Intermediate in the Synthesis of Highly Active Fluorinated Corticosteroids from Phytosterols
- Autores: Karpova N.V.1, Stytsenko T.S.1, Yaderets V.V.1, Andryushina V.A.1, Dzhavakhiya V.V.1
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Afiliações:
- Bioengineering Institute, Biotechnology Research Center, Russian Academy of Sciences
- Edição: Volume 55, Nº 1 (2019)
- Páginas: 37-40
- Seção: Article
- URL: https://journals.rcsi.science/0003-6838/article/view/152768
- DOI: https://doi.org/10.1134/S0003683819010071
- ID: 152768
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Resumo
A method of phytosterol conversion into 9α-hydroxy-androstenedione under high loads of steroid substrate has been developed with the use of mixed cultures of the actinobacteria M. neoaurum and R. erythropolis. The introduction of a 9α-hydroxylating culture after the first 70 h of conversion made it possible to increase process selectivity and to exclude the use of methylcyclodextrin, which is expensive and difficult to regenerate.
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Sobre autores
N. Karpova
Bioengineering Institute, Biotechnology Research Center, Russian Academy of Sciences
Email: andryushina@rambler.ru
Rússia, Moscow, 119071
T. Stytsenko
Bioengineering Institute, Biotechnology Research Center, Russian Academy of Sciences
Email: andryushina@rambler.ru
Rússia, Moscow, 119071
V. Yaderets
Bioengineering Institute, Biotechnology Research Center, Russian Academy of Sciences
Email: andryushina@rambler.ru
Rússia, Moscow, 119071
V. Andryushina
Bioengineering Institute, Biotechnology Research Center, Russian Academy of Sciences
Autor responsável pela correspondência
Email: andryushina@rambler.ru
Rússia, Moscow, 119071
V. Dzhavakhiya
Bioengineering Institute, Biotechnology Research Center, Russian Academy of Sciences
Email: andryushina@rambler.ru
Rússia, Moscow, 119071
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