Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 127-132 |
| Seitenumfang | 6 |
| Fachzeitschrift | Biotechnology Techniques |
| Jahrgang | 2 |
| Ausgabenummer | 2 |
| Publikationsstatus | Veröffentlicht - Feb. 1988 |
Abstract
The enantioselective hydrolysis of racemic 4-acetoxy-cyclopentenone by immobilized enzymes is described. Liquid membrane emulsions were used to encapsulate the enzyme. This technique combines the specific enzymatic reaction with a selective transport through the organic phase. The product (-)-4-hydroxy-cyclopentenone was produced with an enantiomeric excess of 82%. The immobilization techniques and all reaction steps, as well as a mathematical model for the complete process are discussed in this report.
ASJC Scopus Sachgebiete
- Biochemie, Genetik und Molekularbiologie (insg.)
- Biochemie
- Immunologie und Mikrobiologie (insg.)
- Angewandte Mikrobiologie und Biotechnologie
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in: Biotechnology Techniques, Jahrgang 2, Nr. 2, 02.1988, S. 127-132.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Immobilization of enzymes in liquid membranes for enantioselective hydrolysis
AU - Meyer, E. R.
AU - Scheper, T.
AU - Hitzmann, B.
AU - Schügerl, K.
PY - 1988/2
Y1 - 1988/2
N2 - The enantioselective hydrolysis of racemic 4-acetoxy-cyclopentenone by immobilized enzymes is described. Liquid membrane emulsions were used to encapsulate the enzyme. This technique combines the specific enzymatic reaction with a selective transport through the organic phase. The product (-)-4-hydroxy-cyclopentenone was produced with an enantiomeric excess of 82%. The immobilization techniques and all reaction steps, as well as a mathematical model for the complete process are discussed in this report.
AB - The enantioselective hydrolysis of racemic 4-acetoxy-cyclopentenone by immobilized enzymes is described. Liquid membrane emulsions were used to encapsulate the enzyme. This technique combines the specific enzymatic reaction with a selective transport through the organic phase. The product (-)-4-hydroxy-cyclopentenone was produced with an enantiomeric excess of 82%. The immobilization techniques and all reaction steps, as well as a mathematical model for the complete process are discussed in this report.
UR - http://www.scopus.com/inward/record.url?scp=0342815273&partnerID=8YFLogxK
U2 - 10.1007/BF01876163
DO - 10.1007/BF01876163
M3 - Article
AN - SCOPUS:0342815273
VL - 2
SP - 127
EP - 132
JO - Biotechnology Techniques
JF - Biotechnology Techniques
SN - 0951-208X
IS - 2
ER -