Abstract
The production of single enantiomer chemicals is a key research target for a wide variety of industries due to regulatory concerns over the potential toxicities of the 'inactive' enantiomers in racemates, together with the need for improved dosage efficiency. Enzymatic routes via specific biotransformations can, sometimes, present advantages over asymmetric chemical synthesis. However, large scale biotransformations are often constrained by practical difficulties such as: substrate solubility in aqueous systems; product inhibition, and; further metabolism of the product(s). One novel approach to minimising these problems is to encapsulate the cells in a water in oil (w/o) microemulsion which can supply substrate to cells and remove the end product while providing the cell with an aqueous environment. In this work a microemulsion system was selected to solubilise cells of a Mycobacterium sp. capable of stereospecific epoxidation. This consisted of (Tween 85 and Span 80)/n-hexadecane, and was found to give an optimum water capacity (W0 = mole of water/mol of surfactant) of 25 at an hydrophilic-lipophilic balance (HLB) of the surfactant mixture of 10. The microemulsion could solubilise cell concentrations of up to 0.36 g dm-3, but this system was only stable for 2 h, while at 0.22 g dm-3 it was stable for 9 h. (C) 2000 Elsevier Science B.V.
Original language | English |
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Pages (from-to) | 177-186 |
Number of pages | 10 |
Journal | Colloids and Surfaces A: Physicochemical and Engineering Aspects |
Volume | 166 |
Issue number | 1-3 |
Early online date | 14 Feb 2000 |
DOIs | |
Publication status | Published - 15 Jun 2000 |
Keywords
- Biotransformation
- Cell encapsulation
- Chiral epoxide
- Water in oil microemulsion
ASJC Scopus subject areas
- Surfaces and Interfaces
- Physical and Theoretical Chemistry
- Colloid and Surface Chemistry