2009
DOI: 10.1016/j.molcatb.2008.09.003
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Transformation of C19-steroids and testosterone production by sterol-transforming strains of Mycobacterium spp.

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Cited by 36 publications
(30 citation statements)
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“…and ergosterol (98.5 mg) 6.1% to dry wt. Egorova et al (2009) reported that the formation of testosterone from androstadiendione by sterol-transforming strains of Mycobacterium spp reached maximum level of 0.21 mM (6%) at neutral pH, and decreased at the acid or basic pH values, which clearly correlates with the results obtained in the present study.…”
Section: Resultssupporting
confidence: 92%
“…and ergosterol (98.5 mg) 6.1% to dry wt. Egorova et al (2009) reported that the formation of testosterone from androstadiendione by sterol-transforming strains of Mycobacterium spp reached maximum level of 0.21 mM (6%) at neutral pH, and decreased at the acid or basic pH values, which clearly correlates with the results obtained in the present study.…”
Section: Resultssupporting
confidence: 92%
“…the free and conjugated forms (glucuronides and sulfates) (Mota et al, 2014). When entering the pond of F3, some residual conjugated steroids are likely deconjugated into free forms (Gomes et al, 2009) or converted from some other steroids with similar molecular structures (Egorova et al, 2009;Jenkins et al, 2004). Ten synthetic steroids were detected in water samples of the aquaculture farms (Table 1).…”
Section: Resultsmentioning
confidence: 99%
“…An important pharmaceutical androgen—testosterone—can also be the product of microbiological transformation of sterols. Testosterone is obtained from the AD(D) either by a four-step chemical synthesis, or using microbial 17β-reduction by yeasts or fungi [55]. Microbial conversion of sterols to testosterone by using the strains capable of both sterol side chain cleavage and 17β-reduction of AD allows formation of testosterone in one biotechnological step.…”
Section: Production Of Optically Active Compoundsmentioning
confidence: 99%
“…The strain of Mycobacterium sp. VKM Ac-1815D, capable of sterol side chain degradation and expressing 17β-hydroxysteroid dehydrogenase activity, converted β-sitosterol (5 g/L) to testosterone with 50%–55% molar yield [55]. …”
Section: Production Of Optically Active Compoundsmentioning
confidence: 99%