| RRC ID |
15441
|
| Author |
Yamada-Onodera K, Norimoto A, Kawada N, Furuya R, Yamamoto H, Tani Y.
|
| Title |
Production of optically active 1,2,4-butanetriol from corresponding racemate by Microbial stereoinversion.
|
| Journal |
J Biosci Bioeng
|
| 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.
|
| Volume |
103(5)
|
| Pages |
494-6
|
| Published |
2007-5-1
|
| DOI |
10.1263/jbb.103.494
|
| PII |
S1389-1723(07)70094-4
|
| PMID |
17609168
|
| MeSH |
Butanols / chemistry*
Butanols / isolation & purification*
Oxidation-Reduction
Stereoisomerism
Streptomyces / metabolism*
|
| IF |
2.366
|
| Times Cited |
10
|
|
WOS Category
|
FOOD SCIENCE & TECHNOLOGY
BIOTECHNOLOGY & APPLIED MICROBIOLOGY
|
| Resource |
| General Microbes |
JCM 1747
JCM 2467
JCM 5222 |
