Bicontinuous Microemulsion as Reaction Medium for ω-Transaminase Catalysed Biotransformations

被引:8
作者
Laupheimer, M. [1 ]
Engelskirchen, S. [1 ]
Tauber, K. [2 ]
Kroutil, W. [2 ]
Stubenrauch, C. [1 ]
机构
[1] Univ Stuttgart, Inst Phys Chem, D-70569 Stuttgart, Germany
[2] Karl Franzens Univ Graz, Inst Chem Organ & Bioorgan Chem, Graz, Austria
关键词
Bicontinuous microemulsion; biotransformation; enzyme reaction; enzyme-substrate incompatibility; reaction medium; IN-OIL MICROEMULSIONS; WATER; LIPASE; KINETICS; MICELLAR;
D O I
10.3139/113.110100
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Due to their high enantioselectivity biotransformations, i.e. enzyme-catalysed conversion of organic compounds, are extremely attractive reactions. However, a limiting factor for choosing substrates is the enzyme-substrate incompatibility. This occurs when a hydrophilic enzyme which naturally resides in the aqueous cell cytoplasm is supposed to convert a hydrophobic substrate. In this context bicontinuous microemulsions appear to be a beneficial reaction medium for biotransformations, particularly due to their large interfacial area between a hydrophilic and a hydrophobic compound. As a "proof of concept" we performed omega-transaminase (EC 2.6.1.18) catalysed model reactions in a bicontinuous microemulsion of the type phosphate buffer/NaCl - n-octane - pentaethylene glycol monodecyl ether.
引用
收藏
页码:28 / 33
页数:6
相关论文
共 22 条
[1]   Kinetics of reactions catalyzed by enzymes in solutions of surfactants [J].
Biasutti, Maria A. ;
Abuin, Elsa B. ;
Silber, Juana J. ;
Correa, N. Mariano ;
Lissi, Eduardo A. .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2008, 136 (1-2) :1-24
[2]   On microemulsion phase behavior and the monomeric solubility of surfactant [J].
Burauer, S ;
Sachert, T ;
Sottmann, T ;
Strey, R .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1999, 1 (18) :4299-4306
[3]   Lipase-catalysed interfacial reactions in reverse micellar systems - Role of water and microenvironment in determining enzyme activity or dormancy [J].
Carlile, K ;
Rees, GD ;
Robinson, BH ;
Steer, TD ;
Svensson, M .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1996, 92 (23) :4701-4708
[4]  
Chai JL, 2004, CHINESE CHEM LETT, V15, P699
[5]  
ENGELSKIRCHEN S, 2005, PHYSIKOCHEMISCHEN GR
[6]   Biotransformations of non-natural compounds: State of the art and future development [J].
Faber, K .
PURE AND APPLIED CHEMISTRY, 1997, 69 (08) :1613-1632
[7]  
Gupta S, 2003, INDIAN J BIOCHEM BIO, V40, P340
[8]  
Jenta TRJ, 1997, BIOTECHNOL BIOENG, V54, P416, DOI 10.1002/(SICI)1097-0290(19970605)54:5<416::AID-BIT2>3.0.CO
[9]  
2-H
[10]   Deracemisation of α-Chiral Primary Amines by a One-Pot, Two-Step Cascade Reaction Catalysed by ω-Transaminases [J].
Koszelewski, Dominik ;
Clay, Dorina ;
Rozzell, David ;
Kroutil, Wolfgang .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2009, 2009 (14) :2289-2292