| Literature DB >> 17609168 |
Keiko Yamada-Onodera1, Akihiro Norimoto, Naoki Kawada, Rika Furuya, Hiroaki Yamamoto, Yoshiki Tani.
Abstract
Sterigmatomyces elviae DSM 70852 produced 12 g/l (S)-1,2,4-butanetriol (enantiomeric excess >99.9%) from 20 g/l racemate in 82 h. From the results of the inversion of an (R)-isomer to an (S)-isomer and GC-MS, it was suggested that (R)-1,2,4-butanetriol is oxidized to 1,4-dihydroxy-2-butanone, which is reduced to an (S)-isomer.Entities:
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Year: 2007 PMID： 17609168 DOI： 10.1263/jbb.103.494
Source DB: PubMed Journal: J Biosci Bioeng ISSN： 1347-4421 Impact factor: 2.894