Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ali Kerridge"'
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 22:219-223
A version of Rhodococcus erythropolis IGTS8 BKO-53, designed as a model system for the biodesulfurization of crude oil with a high conversion activity of dibenzothiophenes to the corresponding sulfoxides has been used for oxidation of a large number
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d047add19d66b888056b5a36b0611ae4
https://doi.org/10.1016/s1381-1177(03)00040-7
https://doi.org/10.1016/s1381-1177(03)00040-7
Autor:
Dean V. Johnson, Benjamin Mayne, Herbert L. Holland, Frances M. Brown, Carl D Turner, Aaron J van Vliet, Ali Kerridge
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 17:249-256
Treatment of N -methoxycarbonyl C -carboxylate ester derivatives of S -methyl- l -cysteine by chloroperoxidase (CPO)/hydrogen peroxide resulted in oxidation at sulfur to produce the ( R S ) sulfoxide in moderate to high diastereomeric excess (DE). Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d03f2cd4d64226444072c27a37f00098
https://doi.org/10.1016/s1381-1177(02)00041-3
https://doi.org/10.1016/s1381-1177(02)00041-3
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 6:463-471
Benzyl methyl sulfides substituted with methyl, chloro, cyano, bromo, methoxy, nitro and amino groups in the ortho or meta positions of the aromatic ring have been converted to ( S ) sulfoxides by biotransformation using the fungal biocatalyst Helmin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23bf46196e165dabe034dc45536b5016
https://doi.org/10.1016/s1381-1177(99)00006-5
https://doi.org/10.1016/s1381-1177(99)00006-5
Publikováno v:
Biocatalysis and Biotransformation. 17:305-317
Para-substituted phenyl 3-chloropropyl and phenyl 3-hydroxypropyl sulfides have been oxidised to the corresponding (R)-sulfoxides by biotransformation with Mortierella isabellina ATCC 42613, and to the (S)-sulfoxides by biotransformation with Helmint
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e233d75c0bb48e7d942c8e635c009044
https://doi.org/10.3109/10242429909015233
https://doi.org/10.3109/10242429909015233
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 6:59-65
Washed-cell preparations of recombinant Escherichia coli JM109(pDTG141), engineered to express the naphthalene dioxygenase (NDO) gene from Pseudomonas sp. NCIB 9816-4, have been used to biooxidise a range of aryl alkyl-, dialkyl- and bicyclic sulfide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81de99d4a5c1a9b47025c6f4ed85a4ef
https://doi.org/10.1016/s1381-1177(98)00121-0
https://doi.org/10.1016/s1381-1177(98)00121-0
Autor:
Nicholas J. Turner, Ali Kerridge, Julian S. Parratt, Fritz Theil, Stanley M. Roberts, Andrew Willetts
Publikováno v:
Bioorganic & Medicinal Chemistry. 2:447-455
The enantiomerically pure (S)-cyano acids 3 and 4 can be obtained by biotransformation with Brevibacterium sp. R 312 of the corresponding prochiral dinitriles 5 and 6, respectively. The hydrolysis is probably a two step process involving a nitrile hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c041406be24260f15401b08f5a0ee387
https://doi.org/10.1016/0968-0896(94)80014-6
https://doi.org/10.1016/0968-0896(94)80014-6
Publikováno v:
Biocatalysis & Biotransformation; 1999, Vol. 17 Issue 4, p305-317, 13p