Synthesis of 3β-methyl ether of dehydroepiandrosterone by biotransformation of 3β-methyl ether of cholesterol with cells of mycobacteria Mycobacterium sp.
- Authors: Andryushina V.A.1, Stytsenko T.S.1, Karpova N.V.1, Yaderets V.V.1, Zavarzin I.V.2, Kurilov D.V.2
- 
							Affiliations: 
							- Federal Research Center “Fundamentals of Biotechnology”, Russian Academy of Sciences
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
 
- Issue: Vol 68, No 12 (2019)
- Pages: 2355-2358
- Section: Full Articles
- URL: https://journals.rcsi.science/1066-5285/article/view/243571
- DOI: https://doi.org/10.1007/s11172-019-2711-0
- ID: 243571
Cite item
Abstract
3p-Methyl ether of dehydroepiandrosterone was obtained by microbiological transformation of 3ß-methyl ether of cholesterol with Mycobacterium sp. Androstane-3,17-dione, androst-4-ene-3,17-dione, and androsta-1,4-diene-3,17-dione were minor transformation products.
About the authors
V. A. Andryushina
Federal Research Center “Fundamentals of Biotechnology”, Russian Academy of Sciences
							Author for correspondence.
							Email: andryushina@rambler.ru
				                					                																			                												                	Russian Federation, 							korp.1, 7 prosp. 60-letiya Oktyabrya, Moscow, 117312						
T. S. Stytsenko
Federal Research Center “Fundamentals of Biotechnology”, Russian Academy of Sciences
														Email: kur-dv@mail.ru
				                					                																			                												                	Russian Federation, 							korp.1, 7 prosp. 60-letiya Oktyabrya, Moscow, 117312						
N. V. Karpova
Federal Research Center “Fundamentals of Biotechnology”, Russian Academy of Sciences
														Email: kur-dv@mail.ru
				                					                																			                												                	Russian Federation, 							korp.1, 7 prosp. 60-letiya Oktyabrya, Moscow, 117312						
V. V. Yaderets
Federal Research Center “Fundamentals of Biotechnology”, Russian Academy of Sciences
														Email: kur-dv@mail.ru
				                					                																			                												                	Russian Federation, 							korp.1, 7 prosp. 60-letiya Oktyabrya, Moscow, 117312						
I. V. Zavarzin
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
														Email: kur-dv@mail.ru
				                					                																			                												                	Russian Federation, 							47 Leninsky prosp., Moscow, 119991						
D. V. Kurilov
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
							Author for correspondence.
							Email: kur-dv@mail.ru
				                					                																			                												                	Russian Federation, 							47 Leninsky prosp., Moscow, 119991						
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