Antioxidant polysaccharides were synthesized using an innovative, green, enzymatic reaction to catalyze the grafting of ferulic acid (FA) onto pullulan (Pull). Several grades of Pull-FA with verified purity were successfully synthesized, with maximum experimental grafting rates (GR) up to 8.8%, as determined by the Folin Ciocalteu method. For the first time, the chemical structure of the grafts was proposed using 13C solid-state NMR and MALDI-TOF MS analyses, which proposed the putative grafting of a negatively charged, monodecarboxylated FA dimer (β-5). SEC/MALS/DRI/UV/visco analyses confirmed the grafting with a tendency towards intra- and intermolecular hydrophobic self-association, which depends on the grafting rate. The aggregative power of Pull-FAs in dilute medium as a function of the grafting rate and the pH of the medium was highlighted using the Nile red fluorescent probe and light scattering. In semi-dilute/concentrated media, intermolecular self-association was revealed by an increase in texture and a reversible physical gel behavior under favorable pH conditions. DPPH• analyses showed the antioxidant activity of Pull-FAs and confirmed the linear decrease in EC50 as a function of grafting rate.
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