Enantiomerically pure D-phenylglycine production using immobilized Pseudomonas aeruginosa 10145 in calcium alginate beads

14Citations
Citations of this article
9Readers
Mendeley users who have this article in their library.

Abstract

In a preliminary work in our laboratory, a Pseudomonas aeruginosa strain was found to have enzymatic activity to convert arylaminonitriles into D-amino acids. This enzymatic activity was increased by induction to produce enantiomerically pure D-phenylglycine using 2-phenyl-2-aminoacetonitrile as starting material. In this work, the best conditions leading to this transformation are described. In order to increase the biocatalyst potential use, cells of Pseudomonas aeruginosa 10145 were entrapped in calcium alginate gel beads. Two different concentration of sodium alginate were used to immobilize these cells. Beads morphology was demonstrated by scanning electron microscopy (SEM). The beads with higher porosity, formed with 1.5% (m/v) of sodium alginate led to the best conversion of 2-phenyl-2-aminoacetonitrile into D-phenylglycine (20% of conversion, 3.0 h of reaction enantiomeric excess higher than 98%). Recycling was performed in four repeated batch reactions, which proved the biocatalyst activity maintenance. ©2007 Sociedade Brasileira de Química.

Cite

CITATION STYLE

APA

Alonso, F. O. M., Antunes, O. A. C., & Oestreicher, E. G. (2007). Enantiomerically pure D-phenylglycine production using immobilized Pseudomonas aeruginosa 10145 in calcium alginate beads. Journal of the Brazilian Chemical Society, 18(3), 566–571. https://doi.org/10.1590/S0103-50532007000300011

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free