Effect of carboxymethylation on antioxidant properties and radical degradation of mannans and glucans

Carbohydr Polym. 2014 Nov 4:112:603-7. doi: 10.1016/j.carbpol.2014.06.050. Epub 2014 Jun 24.

Abstract

Carboxymethyl derivatives (CM-derivatives) of α,β-mannans from yeasts, Saccharomyces cerevisiae β-glucan and dextran (α-glucan) were found to possess strong antioxidant activities against reactive hydroxyl radicals (OH*) compared to underivatized polysaccharides. When CM-derivatives having similar DS (0.41-0.45) were compared, the antioxidant activity decreased in order CM-mannan>CM-β-glucan>CM-dextran. Moreover, the antioxidant activities against OH* increased with increasing degree of substitution (DS) of polysaccharides. The CM-mannan and CM-dextran with the highest DS (0.73 and 1.1, respectively) were the strongest antioxidants and their degradation by OH* decreased with increased carboxymethylation. The scavenging abilities of CM-polysaccharides against stable DPPH radical (DPPH) were lower than those of original underivatized ones. Also this scavenging property against DPPH was lower compared to antioxidant effect against OH*.

Keywords: Antioxidant activity; Carboxymethyl polysaccharides; Degradation by OH.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants / chemistry
  • Antioxidants / pharmacology*
  • Candida / chemistry
  • Free Radical Scavengers / chemistry
  • Free Radical Scavengers / pharmacology
  • Glucans / chemistry*
  • Glucans / metabolism
  • Glucans / pharmacology*
  • Hydroxyl Radical / metabolism
  • Iron Chelating Agents / chemistry
  • Iron Chelating Agents / pharmacology
  • Mannans / chemistry*
  • Mannans / metabolism
  • Mannans / pharmacology*
  • Saccharomyces cerevisiae / chemistry
  • Structure-Activity Relationship

Substances

  • Antioxidants
  • Free Radical Scavengers
  • Glucans
  • Iron Chelating Agents
  • Mannans
  • Hydroxyl Radical