Chemical improvement of chitosan-modified beads for the immobilization of Enterococcus faecium DBFIQ E36 l-arabinose isomerase through multipoint covalent attachment approach

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Abstract
D-tagatose is produced from d-galactose by the enzyme l-arabinose isomerase (L-AI) in a commercially viable bioprocess. An active and stable biocatalyst was obtained by modifying chitosan gel structure through reaction with TNBS, d-fructose or DMF, among others. This led to a significant improvement in L-AI immobilization via multipoint covalent attachment approach. Synthetized derivatives were compared with commercial supports such as Eupergit® C250L and glyoxal-agarose. The best chitosan derivative for L-AI immobilization was achieved by reacting 4 % (w/v) d-fructose with 3 % (w/v) chitosan at 50 °C for 4 h. When compared to the free enzyme, the glutaraldehyde-activated chitosan biocatalyst showed an apparent activity of 88.4 U ggel −1 with a 211-fold stabilization factor while the glyoxal-agarose biocatalyst gave an apparent activity of 161.8 U ggel −1 with an 85-fold stabilization factor. Hence, chitosan derivatives were comparable to commercial resins, thus becoming a viable low-cost strategy to obtain high active L-AI insolubilized derivatives.
Funding Information
  • Universidad Nacional del Litoral (AR) (CAI+D 2011 501 201101 00357 LI)
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (BR) (Argentina–Brazil Bilateral Cooperation Program BR/12/06 MINCyT-CAPES 2012)
  • Ministerio de Ciencia, Tecnología e Innovación Productiva (AR) (Argentina-Brasil Bilateral Cooperation Program BR/12/06)
  • Agencia Nacional de Promoción Científica y Tecnológica (AR)

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