Process for the stereoselective preparation of...

Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing oxygen-containing organic compound

Reexamination Certificate

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C435S145000, C435S195000, C435S196000, C435S254200

Reexamination Certificate

active

07022503

ABSTRACT:
The present invention relates to a process for the kinetic resolution of racemic functionalized epoxides in the presence of microorganisms, crude or pure preparations thereof comprising a polypeptide having epoxide hydrolase activity. Preferred microorganisms are yeasts and bacteria which may also be recombinant.

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Weijers, Carel A. G. M. et al;“Epoxide hydrolases from yeasts and other sources: versatile tools in biocatalysis” retrieved from STN Database accession No. 130:293060, XP002189633 *abstract* & J. Mol. Catal. B: Enzym. (1999), 6(3), 199-214.
Krenn, Wolfram et al. “Bacterial epoxide hydrolases of opposite enantiopreference” retrieved from STN Database accession No. 131:333942, XP002189634 *abstract* & Biotechnol. Lett. (1999), 21(8), 687-690.
Greene J. F. et al: “Metabolism of monoepoxides of methyl linoleate: Bioactivation and detoxification.” Archives of Biochemistry and Biophysics, vol. 376, No. 2, 2000, pp. 420-432, XP002189628.
Blee E. and Schuber F.: “Regio- and Enantioselectivity of Soybean Fatty Acid Epoxide Hydrolase.” J. Biol. Chem. vol. 267, No. 17, 1992, pp. 11881-1187, XP002189629, see especially p. 11886 *the whole document*.
Visser , H. et al: “Cloning and characterization of an epoxide hydrolase-encoding gene fromRhodotorula glutinis”retrieved from STN, Database accession No. 133:234299, XP002189630 *abstract* & Appl. Microbiol. Biotechnol. (2000), 53(4), 415-419.
Weijers, Carel A. G. M.: “Enantioselective hydrolysis of aryl, alicyclic and allphatic epoxides byRhodotorula glutinis”retrieved from STN Database accession No. 126:263661, XP002189631 *abstract* & Tetrahedron: Asymmetry (1997), 8(4), 639-647.
Botes, A. L. et al: “Biocatalytic resolution of 1,2-epoxyoctane using resting cells of different yeast strains with novel epoxide hydrolase activities” retrieved from STN Database accession No. 129:25538, XP002189632 *abstract* & Biotachnol. Lett. (1998), 20(4), 421-426.

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