Kinetics of the lipase-catalyzed synthesis of glucose esters in acetone
β Scribed by Jose A. Arcos; Charles G. Hill Jr.; Cristina Otero
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 125 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0006-3592
- DOI
- 10.1002/bit.1042
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π SIMILAR VOLUMES
Racemic amino acids were resolved by lipase via hydrolysis of their esters. Lipases (Pseudomonas lipase from Amano PS, Rhizopus lipase from Serva, and porcine pancrease lipase from Sigma) could selectively hydrolyze the L-amino acid esters in aqueous solution with high reactivities and selectivities
## Abstract A kinetic model derived from the pingβpong biβbi reversible mechanism is proposed to described the acylation of glucose by lauric acid in 2βmethyl 2βbutanol mediated by __Candida antarctica__ lipase at 60Β°C. The model accounts for the effect of all four compounds in the reaction mixture