Issue 64, 2014

Enantioselective transesterification of (R,S)-2-pentanol catalyzed by a new flower-like nanobioreactor

Abstract

The lipase-incorporated nanoflower was prepared and used for resolution of (R,S)-2-pentanol with vinyl acetate as an acyl donor in organic solvents. SEM images indicated that the lipase-incorporated nanoflower had high surface area which was favourable for mass transfer. The FTIR spectrum identified the presence of the lipase in the nanoflower. The lipase-incorporated nanoflower could display its maximum enzyme activity (22.5 μmol h−1 mg−1) and good enantioselectivity (E value, 47.3) under the optimal reaction conditions (in cyclohexane at 60 °C and water activity of 0.10). After ten continuous batches, the nanoflower retained 98.7% of the initial enzyme activity and 95.6% of the initial enantioselectivity.

Graphical abstract: Enantioselective transesterification of (R,S)-2-pentanol catalyzed by a new flower-like nanobioreactor

Article information

Article type
Paper
Submitted
12 May 2014
Accepted
29 Jul 2014
First published
30 Jul 2014

RSC Adv., 2014,4, 33998-34002

Author version available

Enantioselective transesterification of (R,S)-2-pentanol catalyzed by a new flower-like nanobioreactor

Z. Wu, X. Li, F. Li, H. Yue, C. He, F. Xie and Z. Wang, RSC Adv., 2014, 4, 33998 DOI: 10.1039/C4RA04431B

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