Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Jadwiga Dmochowska-Gładysz"'
Autor:
Tomasz Janeczko, D. Chmolowska, Monika Dymarska, Jadwiga Dmochowska-Gładysz, Ewa Kozłowska, Alina Świzdor, Edyta Kostrzewa-Susłow
Publikováno v:
PRZEMYSŁ CHEMICZNY. 1:195-199
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4e6ebddabc9e478bd33de1593da25b0
https://doi.org/10.15199/62.2016.8.41
https://doi.org/10.15199/62.2016.8.41
Autor:
Tomasz Janeczko, Monika Dymarska, Alina Świzdor, Jadwiga Dmochowska-Gładysz, Ewa Kozłowska, Edyta Kostrzewa-Susłow
Publikováno v:
PRZEMYSŁ CHEMICZNY. 1:99-101
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::128385a23219d72bd37a8d97a29cd71d
https://doi.org/10.15199/62.2016.9.15
https://doi.org/10.15199/62.2016.9.15
Autor:
Tomasz Janeczko, Jadwiga Dmochowska-Gładysz, Ewa Walczak, Edyta Kostrzewa-Susłow, Małgorzata Robak, Wojciech Bąkowski
Publikováno v:
Annals of Microbiology
The ability of 16 strains of Yarrowia lipolytica to biotransform acetophenone and its derivatives has been studied. Thirteen of these strains were derived from a wild-type strain Y. lipolytica A-101; six had the invertase gene (SUC2) from Saccharomyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::622bf869731eed96dc4dac8942339be9
https://doi.org/10.1007/s13213-014-0955-3
https://doi.org/10.1007/s13213-014-0955-3
Autor:
Jadwiga Dmochowska-Gładysz, Agata Białońska, Edyta Kostrzewa-Susłow, Zbigniew Ciunik, Alina Świzdor, Tomasz Janeczko
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 82:24-31
Dehydroepiandrosterone (DHEA) (10) and its five derivatives: testosterone (1), androstenedione (2), 17α-methyltestosterone (6), progesterone (13) and pregnenolone (14) were subjected to microbial transformation by the filamentous fungus Didymosphaer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e40da3059cb7c1e5fef798638280205a
https://doi.org/10.1016/j.molcatb.2012.05.009
https://doi.org/10.1016/j.molcatb.2012.05.009
Autor:
Jadwiga Dmochowska-Gładysz, Tomasz Janeczko, Edyta Kostrzewa-Susłow, Anna Panek, Alina Świzdor
Publikováno v:
Current Microbiology
α-Tetralone and β-tetralone were subjected to biotransformation by 14 fungal strains. Enantiomeric purity of the products depended on the reaction time. 3-Day transformation of α-tetralone in Absidia cylindrospora culture gave S-(+)-1,2,3,4-tetrah
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22bbceadf21b11e004b89008f24f5387
https://doi.org/10.1007/s00284-012-0143-2
https://doi.org/10.1007/s00284-012-0143-2
Publikováno v:
World Journal of Microbiology and Biotechnology. 26:2047-2051
Enantiospecific microbial reduction of bicyclic ketones was described. Racemic Wieland–Miescher (1) and Hajos–Parrish (2) ketones were used as substrates. In a 4-h biotransformation of Hajos–Parrish ketone (2) using the strain of Didymosphaeria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a721d2e86b9931653be3366284c9d46a
https://doi.org/10.1007/s11274-010-0390-y
https://doi.org/10.1007/s11274-010-0390-y
Autor:
Zbigniew Ciunik, Tomasz Janeczko, Agata Białońska, Edyta Kostrzewa-Susłow, Jadwiga Dmochowska-Gładysz
Publikováno v:
Steroids. 74:657-661
Biotransformations of steroid compounds: androstenedione, testosterone, progesterone, pregnenolone and DHEA using Chaetomium sp. 1 KCH 6651 strain as a biocatalyst were investigated. The microorganism proved capable of selective hydroxylation of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97eb326651a3d23be595cd83780c988e
https://doi.org/10.1016/j.steroids.2009.02.006
https://doi.org/10.1016/j.steroids.2009.02.006
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. :34-39
As a result of biotransformation of flavanone ( 1 ) by the strain Aspergillus niger MB (being the UV mutant) and by the wild strain Penicillium chermesinum 113 the products of hydroxylation at C-6 ( 2 ) and C-4′ ( 5 ) were obtained. Additionally, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08579be82ea414284a3c77b1990f83de
https://doi.org/10.1016/j.molcatb.2008.01.002
https://doi.org/10.1016/j.molcatb.2008.01.002
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 49:113-117
As a result of microbial transformation of baicalin and baicalein the products of 4 -hydroxylation of the B ring, O -methylation at C-6, and both O -methylation at C-6 and hydroxylation at C-4 were obtained. Transformations of baicalin were accompani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19c695a0fb12f396e51d54cc15b2616b
https://doi.org/10.1016/j.molcatb.2007.08.009
https://doi.org/10.1016/j.molcatb.2007.08.009
Publikováno v:
Enzyme and Microbial Technology. 40:1615-1621
Trichoderma hamatum KCh25 was used to study the mode of transformation of a series of 3-oxosteroids. This potential has not been previously examined. The strain promoted 1-dehydrogenation, which have been rarely observed in fungi cultures. The metabo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3107f51a15e85768bb0e4083c486705
https://doi.org/10.1016/j.enzmictec.2006.11.011
https://doi.org/10.1016/j.enzmictec.2006.11.011