Screening of mycelial fungi for 7α- and 7β-hydroxylase activity towards dehydroepiandrosterone
In total, 481 fungal strains were screened for the ability to carry out 7(α/β)-hydroxylation of dehydroepiandrosterone (DHEA, 3β-hydroxy-5-androsten-17-one). Representatives of 31 genera of 15 families and nine orders of ascomycetes, 17 genera of nine families and two orders of zygomycetes, two gene...
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Veröffentlicht in: | Biocatalysis and biotransformation 2007-01, Vol.25 (6), p.434-442 |
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creator | Lobastova, Tatyana G. Gulevskaya, Seraphima A. Sukhodolskaya, Galina V. Turchin, Konstantin F. Donova, Marina V. |
description | In total, 481 fungal strains were screened for the ability to carry out 7(α/β)-hydroxylation of dehydroepiandrosterone (DHEA, 3β-hydroxy-5-androsten-17-one). Representatives of 31 genera of 15 families and nine orders of ascomycetes, 17 genera of nine families and two orders of zygomycetes, two genera of two families and two orders of basidiomycetes, and 14 genera of mitosporic fungi expressed 7(α/β)-hydroxylase activity. The majority of strains were able to introduce a hydroxyl group to position 7α. Active strains selectively producing 3β,7α-dihydroxy-5-androsten-17-one were found among Actinomucor, Backusella, Benjaminiella, Epicoccum, Fusarium, Phycomyces and Trichothecium, with the highest yield of 1.25 and 1.9 g L
−1
from 2 and 5 g L
−1
DHEA, respectively, reached with F. oxysporum. Representatives of Acremonium, Bipolaris, Conidiobolus and Curvularia formed 3β,7β-dihydroxy-5-androsten-17-one as a major product from DHEA. The structures of the major steroid products were confirmed by TLC, gas chromatography (GC), mass spectra (MS), and
1
H-NMR analyses. |
doi_str_mv | 10.1080/10242420701568492 |
format | Article |
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−1
from 2 and 5 g L
−1
DHEA, respectively, reached with F. oxysporum. Representatives of Acremonium, Bipolaris, Conidiobolus and Curvularia formed 3β,7β-dihydroxy-5-androsten-17-one as a major product from DHEA. The structures of the major steroid products were confirmed by TLC, gas chromatography (GC), mass spectra (MS), and
1
H-NMR analyses.</description><identifier>ISSN: 1024-2422</identifier><identifier>EISSN: 1029-2446</identifier><identifier>DOI: 10.1080/10242420701568492</identifier><language>eng</language><publisher>Taylor & Francis</publisher><subject>1,4-Androstadiene-3,17-dione ; 4-androstene-3,17-dione ; 7(α/β)-hydroxy dehydroepiandrosterone ; dehydroepiandrosterone ; hydroxylation ; mycelial fungi</subject><ispartof>Biocatalysis and biotransformation, 2007-01, Vol.25 (6), p.434-442</ispartof><rights>2007 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c298t-858520acc7c6fe91d02635965cfacc620da7916890821cfd097168b72294a09c3</citedby><cites>FETCH-LOGICAL-c298t-858520acc7c6fe91d02635965cfacc620da7916890821cfd097168b72294a09c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/10242420701568492$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/10242420701568492$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,59623,60412</link.rule.ids></links><search><creatorcontrib>Lobastova, Tatyana G.</creatorcontrib><creatorcontrib>Gulevskaya, Seraphima A.</creatorcontrib><creatorcontrib>Sukhodolskaya, Galina V.</creatorcontrib><creatorcontrib>Turchin, Konstantin F.</creatorcontrib><creatorcontrib>Donova, Marina V.</creatorcontrib><title>Screening of mycelial fungi for 7α- and 7β-hydroxylase activity towards dehydroepiandrosterone</title><title>Biocatalysis and biotransformation</title><description>In total, 481 fungal strains were screened for the ability to carry out 7(α/β)-hydroxylation of dehydroepiandrosterone (DHEA, 3β-hydroxy-5-androsten-17-one). Representatives of 31 genera of 15 families and nine orders of ascomycetes, 17 genera of nine families and two orders of zygomycetes, two genera of two families and two orders of basidiomycetes, and 14 genera of mitosporic fungi expressed 7(α/β)-hydroxylase activity. The majority of strains were able to introduce a hydroxyl group to position 7α. Active strains selectively producing 3β,7α-dihydroxy-5-androsten-17-one were found among Actinomucor, Backusella, Benjaminiella, Epicoccum, Fusarium, Phycomyces and Trichothecium, with the highest yield of 1.25 and 1.9 g L
−1
from 2 and 5 g L
−1
DHEA, respectively, reached with F. oxysporum. Representatives of Acremonium, Bipolaris, Conidiobolus and Curvularia formed 3β,7β-dihydroxy-5-androsten-17-one as a major product from DHEA. The structures of the major steroid products were confirmed by TLC, gas chromatography (GC), mass spectra (MS), and
1
H-NMR analyses.</description><subject>1,4-Androstadiene-3,17-dione</subject><subject>4-androstene-3,17-dione</subject><subject>7(α/β)-hydroxy dehydroepiandrosterone</subject><subject>dehydroepiandrosterone</subject><subject>hydroxylation</subject><subject>mycelial fungi</subject><issn>1024-2422</issn><issn>1029-2446</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp1UEtOAzEMjRBIlMIB2OUCA05mJh-JDar4SZVYAOsh5FOCpkmVDJQ5FhyEMxFadgh54ednP1t-CB0TOCEg4JQAbUoAB9Iy0Ui6gyaFkxVtGra7wU3BlO6jg5xfAEhNJZ-gxzudrA0-LHB0eDlq23vVY_caFh67mDD_-qiwCqaAz-p5NCm-j73KFis9-Dc_jHiIa5VMxsZu2nbly3iKebApBnuI9pzqsz36zVP0cHlxP7uu5rdXN7PzeaWpFEMlWtFSUFpzzZyVxABldStZq10hGQWjuCRMSBCUaGdA8lI9cUplo0DqeorIdq8up3Oyrlslv1Rp7Ah0PxZ1fywqmrOtxofy6lKtY-pNN6ixj8klFbTPXf2__Bve324S</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>Lobastova, Tatyana G.</creator><creator>Gulevskaya, Seraphima A.</creator><creator>Sukhodolskaya, Galina V.</creator><creator>Turchin, Konstantin F.</creator><creator>Donova, Marina V.</creator><general>Taylor & Francis</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20070101</creationdate><title>Screening of mycelial fungi for 7α- and 7β-hydroxylase activity towards dehydroepiandrosterone</title><author>Lobastova, Tatyana G. ; Gulevskaya, Seraphima A. ; Sukhodolskaya, Galina V. ; Turchin, Konstantin F. ; Donova, Marina V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c298t-858520acc7c6fe91d02635965cfacc620da7916890821cfd097168b72294a09c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>1,4-Androstadiene-3,17-dione</topic><topic>4-androstene-3,17-dione</topic><topic>7(α/β)-hydroxy dehydroepiandrosterone</topic><topic>dehydroepiandrosterone</topic><topic>hydroxylation</topic><topic>mycelial fungi</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lobastova, Tatyana G.</creatorcontrib><creatorcontrib>Gulevskaya, Seraphima A.</creatorcontrib><creatorcontrib>Sukhodolskaya, Galina V.</creatorcontrib><creatorcontrib>Turchin, Konstantin F.</creatorcontrib><creatorcontrib>Donova, Marina V.</creatorcontrib><collection>CrossRef</collection><jtitle>Biocatalysis and biotransformation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lobastova, Tatyana G.</au><au>Gulevskaya, Seraphima A.</au><au>Sukhodolskaya, Galina V.</au><au>Turchin, Konstantin F.</au><au>Donova, Marina V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Screening of mycelial fungi for 7α- and 7β-hydroxylase activity towards dehydroepiandrosterone</atitle><jtitle>Biocatalysis and biotransformation</jtitle><date>2007-01-01</date><risdate>2007</risdate><volume>25</volume><issue>6</issue><spage>434</spage><epage>442</epage><pages>434-442</pages><issn>1024-2422</issn><eissn>1029-2446</eissn><abstract>In total, 481 fungal strains were screened for the ability to carry out 7(α/β)-hydroxylation of dehydroepiandrosterone (DHEA, 3β-hydroxy-5-androsten-17-one). Representatives of 31 genera of 15 families and nine orders of ascomycetes, 17 genera of nine families and two orders of zygomycetes, two genera of two families and two orders of basidiomycetes, and 14 genera of mitosporic fungi expressed 7(α/β)-hydroxylase activity. The majority of strains were able to introduce a hydroxyl group to position 7α. Active strains selectively producing 3β,7α-dihydroxy-5-androsten-17-one were found among Actinomucor, Backusella, Benjaminiella, Epicoccum, Fusarium, Phycomyces and Trichothecium, with the highest yield of 1.25 and 1.9 g L
−1
from 2 and 5 g L
−1
DHEA, respectively, reached with F. oxysporum. Representatives of Acremonium, Bipolaris, Conidiobolus and Curvularia formed 3β,7β-dihydroxy-5-androsten-17-one as a major product from DHEA. The structures of the major steroid products were confirmed by TLC, gas chromatography (GC), mass spectra (MS), and
1
H-NMR analyses.</abstract><pub>Taylor & Francis</pub><doi>10.1080/10242420701568492</doi><tpages>9</tpages></addata></record> |
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subjects | 1,4-Androstadiene-3,17-dione 4-androstene-3,17-dione 7(α/β)-hydroxy dehydroepiandrosterone dehydroepiandrosterone hydroxylation mycelial fungi |
title | Screening of mycelial fungi for 7α- and 7β-hydroxylase activity towards dehydroepiandrosterone |
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