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Functionalization of chitosan by laccase-catalyzed oxidation of ferulic acid and ethyl ferulate under heterogeneous reaction conditions
Authors:Abdulhadi AljawishIsabelle Chevalot,Bernadette PiffautCorinne Rondeau-Mouro,Michel GirardinJordane Jasniewski,Joë  l ScherLionel Muniglia
Affiliation:a Laboratoire d’Ingénierie des Biomolécules (LIBio), Nancy-Université, 2 avenue de la Forêt de Haye, F-54500 Vandœuvre-lès-Nancy, France
b Laboratoire Réactions et Génie des Procédés (LRGP), Nancy-Université, 2 avenue de la Forêt de Haye, F-54500 Vandœuvre-lès-Nancy, France
c Laboratoire de RMN, Plate-forme Biopolymères Biologie Structurale (BiBS), UR1268 BIA-INRA, Rue de la Géraudière, BP 71627, F-44316 Nantes Cedex 3, France
Abstract:Chitosan particles were functionalized with ferulic acid (FA) and ethyl ferulate (EF) as substrates using laccase from Myceliophtora thermophyla as biocatalyst. The reactions were performed with chitosan particles under an eco-friendly procedure, in a heterogeneous system at 30 °C, in phosphate buffer (50 mM, pH 7.5).The FA-chitosan derivative presented an intense yellow-orange color stable while the EF-chitosan derivative was colorless. The spectroscopic analyses indicated that the reaction products bound covalently to the free amino groups of chitosan exhibiting a novel absorbance band in the UV/Vis spectra between 300 and 350 nm, at C-2 region by the duplication of C-2 signal in the 13C NMR spectrum, via Schiff base bond (Ndouble bond; length as m-dashC) exhibiting novel bands in the FT-IR spectrum at 1640 and 1620 cm−1. Additionally, antioxidant capacities of chitosan derivatives showed that the chitosan derivatives presented improved antioxidant properties, especially for FA-chitosan derivative (EC50 were 0.52 ± 0.04, 0.20 ± 0.02 mg/ml for DPPHradical dot and ABTSradical dot+ scavenging, respectively).
Keywords:Chitosan   Enzymatic functionalization   Myceliophtora thermophyla laccase   Ferulic acid   Ethyl ferulate   Antioxidant properties
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