Stereoselective reduction of ethyl 4-chloro-3-oxobutanoate by fungi

Citation
Y. Saratani et al., Stereoselective reduction of ethyl 4-chloro-3-oxobutanoate by fungi, BIOS BIOT B, 65(7), 2001, pp. 1676-1679
Citations number
22
Categorie Soggetti
Agricultural Chemistry","Biochemistry & Biophysics
Journal title
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
ISSN journal
09168451 → ACNP
Volume
65
Issue
7
Year of publication
2001
Pages
1676 - 1679
Database
ISI
SICI code
0916-8451(200107)65:7<1676:SROE4B>2.0.ZU;2-9
Abstract
The enantioselectivity of ECAA to ECHB by eight fungi of four genus was eva luated. All strains showed (S)-selectivity, and Cylindrocarpon sclerotigenu m IFO 31855 gave the highest yield and good optical purity (e.e.; >99%). Ce ll-free extract and acetone-dried cells of C. sclerotigenum IFO 31855 reduc ed ECAA to (S)ECHB in the presence of NADPH (e.e.;>99%) and the e.e. was no t decreased by heat treatment of the cell-free extract or the acetone-dried cells. The active fractions shown by two peaks on a DEAE-Toyopearl 650 M c olumn gave preferentially (S)-ECHB (e.e.; > 99%).