Synthesis of fatty acid esters by a recombinant cutinase in reversed micelles
✍ Scribed by M. J. Sebastião; J. M. S. Cabral; M. R. Aires-Barros
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 587 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0006-3592
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Fusarium solani pisi recombinant cutinase, solubilized in AOT/isooctane‐reversed micelles, was used to catalyze the esterification of fatty acids with aliphatic alcohols. Some relevant parameters for the enzyme activity such as pH, W~o~ (water/surfactant molar ratio), temperature, and substrate concentration were optimized. Maximal specific activity was obtained for hexanol. The cutinase showed selectivity for short‐chain fatty acids. The stability of the microencapsulated cutinase was investigated at various concentrations of water and different values of pH. Oleic acid had a negative effect on the cutinase stability, while hexanol proved to be a strong stabilizer increasing the half‐life of the enzyme about 45 times. © 1993 John Wiley & Sons, Inc.
📜 SIMILAR VOLUMES
## Abstract The effect of solvents and solvent mixtures on the synthesis of myristic acid esters of different carbohydrates with an immobilized lipase from __C. antarctica__ was investigated. The rate of myristyl glucose synthesized by the enzyme was increased from 3.7 to 20.2 μmol min^−1^ g^−1^ by