| Literature DB >> 24731350 |
Suman Kumar Halder1, Arijit Jana1, Arpan Das1, Tanmay Paul1, Pradeep Kumar Das Mohapatra1, Bikas Ranjan Pati1, Keshab Chandra Mondal2.
Abstract
Chitosaccharides (CS) of varied size were prepared from shrimp shell through sequential catalysis, using crude protease and chitinase enzymes immobilized on agar beads. In the optimized state, immobilization yield and activity yield for protease were 84% and 62%, and for chitinase were 75% and 57%, respectively. Immobilized protease and chitinase treatment improved CS yields (101 μg/ml) and retained 63% and 52% of activities after 10 reuses, respectively. Stronger radical-scavenging activity (RSA) of CS against ABTS, DPPH and hydroxyl radical was noted with EC50 values 19.1, 26.4 and 29.6 μg/ml, respectively. Peroxyl and superoxide RSAs of 96.8% and 88.6% were noticed at 70 μg/ml of CS. Singlet oxygen quenching, reducing power and ferrous ion-chelating activities of CS were also pronounced. CS reasonably reduced oxidative damage of DNA, protein and RBC by inhibiting H2O2 and AAPH radicals. Reversible CS-DNA condensation leads to DNA stabilization without changing its conformation and advocates its employment in gene therapy.Entities:
Keywords: Antioxidant; Chitosaccharides; DNA condensation; Enzyme immobilization; Hemolysis inhibition; Shrimp shell
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Year: 2014 PMID: 24731350 DOI: 10.1016/j.foodchem.2014.02.115
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514