Resolution of 1,2-epoxyhexane by Rhodotorula glutinis using a two-phase membrane bioreactor

被引:23
作者
Choi, WJ
Choi, CY
De Bont, JAM
Weijers, CAGM
机构
[1] Wageningen Univ Agr, Dept Food Technol & Nutrit Sci, Div Ind Microbiol, NL-6700 EV Wageningen, Netherlands
[2] Seoul Natl Univ, Dept Chem Technol, Coll Engn, Seoul 151742, South Korea
关键词
D O I
10.1007/s002530051606
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Large-scale resolution of epoxides by the yeast Rhodotorula glutinis was demonstrated in an aqueous/organic two-phase cascade membrane bioreactor. Due to the chemical instability and low solubility of epoxides in aqueous phases, an organic solvent was introduced into the reaction mixture in order to enhance the resolution of epoxide. A cascade hollow-fiber membrane bioreactor was used (1) to minimize the toxicity of organic solvents towards the epoxide hydrolase of R. glutinis, and (2) to remove inhibitory amounts of formed diol from the yeast cell containing aqueous phase. Dodecane was selected as a suitable solvent and 1,2-epoxyhexane as a model substrate. By use of this membrane bioreactor, highly concentrated (0.9 M in dodecane) enantiopure (>98% ee) (S)-1,2-epoxyhexane (6.5 g, 30% yield) was obtained from the racemic mixture.
引用
收藏
页码:7 / 11
页数:5
相关论文
共 14 条
[1]  
Archelas A, 1999, TOP CURR CHEM, V200, P159
[2]   Epoxide hydrolases as asymmetric catalysts [J].
Archer, IVJ .
TETRAHEDRON, 1997, 53 (46) :15617-15662
[3]   CHEMICAL AND BIOLOGICAL SYNTHESIS OF CHIRAL EPOXIDES [J].
BESSE, P ;
VESCHAMBRE, H .
TETRAHEDRON, 1994, 50 (30) :8885-8927
[4]   Kinetic resolution for optically active epoxides by microbial enantioselective hydrolysis [J].
Choi, WJ ;
Huh, EC ;
Park, HJ ;
Lee, EY ;
Choi, CY .
BIOTECHNOLOGY TECHNIQUES, 1998, 12 (03) :225-228
[5]   BIOFORMATION OF OPTICALLY PURE EPOXIDES [J].
DEBONT, JAM .
TETRAHEDRON-ASYMMETRY, 1993, 4 (06) :1331-1340
[6]   A PSEUDOMONAS THRIVES IN HIGH-CONCENTRATIONS OF TOLUENE [J].
INOUE, A ;
HORIKOSHI, K .
NATURE, 1989, 338 (6212) :264-266
[7]   Why are enzymes less active in organic solvents than in water? [J].
Klibanov, AM .
TRENDS IN BIOTECHNOLOGY, 1997, 15 (03) :97-101
[8]  
Orru R V, 1999, Adv Biochem Eng Biotechnol, V63, P145
[9]   Stereoselectivities of microbial epoxide hydrolases [J].
Orru, RVA ;
Faber, K .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (01) :16-21
[10]   Microbiological transformations .37. An enantioconvergent synthesis of the beta-blocker (R)-Nifenalol(R) using a combined chemoenzymatic approach [J].
PedragosaMoreau, S ;
Morisseau, C ;
Baratti, J ;
Zylber, J ;
Archelas, A ;
Furstoss, R .
TETRAHEDRON, 1997, 53 (28) :9707-9714