M V Donova
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Explore the profile of M V Donova including associated specialties, affiliations and a list of published articles.
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25
Citations
185
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Recent Articles
1.
Poshekhontseva V, Fokina V, Tarlachkov S, Machulin A, Shutov A, Donova M
Appl Biochem Microbiol
. 2021 Dec;
57(9):939-948.
PMID: 34924587
The sp. VKM Ac-2618D strain has been identified, and its morphological and physiological features have been studied in relation to the production of the immunosuppressant tacrolimus. The phenotypic variability of...
2.
Bragin E, Shtratnikova V, Dovbnya D, Schelkunov M, Pekov Y, Malakho S, et al.
J Steroid Biochem Mol Biol
. 2020 May;
200:105666.
PMID: 32408066
No abstract available.
3.
Lobastova T, Khomutov S, Shutov A, Donova M
Appl Microbiol Biotechnol
. 2019 Apr;
103(12):4967-4976.
PMID: 31028438
Microbiological synthesis of 7α- and 7β-hydroxy derivatives of testololactone and testolactone was developed based on bioconversion of dehydroepiandrosterone (DHEA) by fungus of Isaria fumosorosea VKM F-881 with subsequent modification of...
4.
Kollerov V, Lobastova T, Monti D, Deshcherevskaya N, E Ferrandi E, Fronza G, et al.
Steroids
. 2016 Jan;
107:20-9.
PMID: 26718089
More than 100 filamentous fungi strains, mostly ascomycetes and zygomycetes from different phyla, were screened for the ability to convert deoxycholic acid (DCA) to valuable bile acid derivatives. Along with...
5.
Lobastova T, Khomutov S, Donova M
Prikl Biokhim Mikrobiol
. 2015 Jun;
51(2):174-82.
PMID: 26027352
The transformation of dehydroepiandrosterone by Spicaria fumoso-rosea VKM F-881 produced 7alpha- and 7beta-hydroxy-dehydroepiandrosterone, 3beta,7alpha-dihydroxy-17a-oxa-D-homo-androst-5-en-17-one, and 3beta,7beta-dihydroxy- 17a-oxa-D-homo-androst-5-en-17-one. The yield of the main product-3beta,7beta-dihydroxy-17a-oxa-D-homo-androst-5-en-17-one-was 49.5-72 mol % at substrate loadings of...
6.
Kollerov V, Fokina V, Sukhodolskaya G, Shutov A, Donova M
Prikl Biokhim Mikrobiol
. 2015 Jun;
51(2):161-73.
PMID: 26027351
Selected filamentous fungi--98 strains of 31 genera--were screened for the ability to catalyze 11beta-hydroxylation of 6alpha-fluoro-16alpha-methyl-deoxycorticosterone 21-acetate (FM-DCA). It was established that representatives of the genera Gongronella, Scopulariopsis, Epicoccum, and...
7.
Bragin E, Shtratnikova V, Dovbnya D, Schelkunov M, Pekov Y, Malakho S, et al.
J Steroid Biochem Mol Biol
. 2013 Mar;
138:41-53.
PMID: 23474435
A comparative genome analysis of Mycobacterium spp. VKM Ac-1815D, 1816D and 1817D strains used for efficient production of key steroid intermediates (androst-4-ene-3,17-dione, AD, androsta-1,4-diene-3,17-dione, ADD, 9α-hydroxy androst-4-ene-3,17-dione, 9-OH-AD) from phytosterol...
8.
Kollerov V, Monti D, Deshcherevskaya N, Lobastova T, E Ferrandi E, Larovere A, et al.
Steroids
. 2013 Jan;
78(3):370-8.
PMID: 23333587
Selected actinobacteria and filamentous fungi of different taxonomy were screened for the ability to carry out regio- and stereospecific hydroxylation of lithocholic acid (LCA) at position 7β. The production of...
9.
Kollerov V, Shutov A, Fokina V, Sukhodolskaia G, Gulevskaia S, Donova M
Prikl Biokhim Mikrobiol
. 2010 Apr;
46(2):212-20.
PMID: 20391766
Regio- and stereospecificity of microbial hydroxylation was studied at the transformation of 3-keto-4-ene steroids of androstane and pregnane series by the filamentous fungus of Curvularia lunata VKMF-644. The products of...
10.
Lobastova T, Gulevskaia S, Sukhodolskaia G, Donova M
Prikl Biokhim Mikrobiol
. 2010 Jan;
45(6):684-9.
PMID: 20067153
The ability of 485 fungal strains is studied for catalysis of the process of 7alpha, 15alpha-dihydroxylation of dehydroepiandrosterone (DHEA, 3alpha-hydroxy-5-androstene-17-one), a key intermediate of the synthesis of physiologically active compounds....