Structural characterization, antifungal and cytotoxic profiles of quaternized heteropolysaccharide from Anadenanthera colubrina

Int J Biol Macromol. 2020 Dec 15;165(Pt A):279-290. doi: 10.1016/j.ijbiomac.2020.09.087. Epub 2020 Sep 18.

Abstract

In the present work, we investigated the minimal inhibitory concentration (MIC) against fungal strains (Fonsecaea pedrosoi, Microsporum canis, Candida albicans, Cryptococcus neoformans), and cytotoxicity to normal cell lines for modified red angico gum (AG) with eterifying agent N-chloride (3-chloro-2-hydroxypropyl) trimethylammonium (CHPTAC). Quaternized ammonium groups were linked to AG backbone using N-(3-chloro-2-hydroxypropyl) trimethylammonium chloride. The chemical features of the quaternized gum derivatives (QAG) were analyzed by: FTIR, elemental analysis, Zeta potential and gel permeation chromatography. The angico quaternizated gum presented a degree of substitution (DS) of 0.22 and Zeta potential of +36.43. For the antifungal test, it was observed that unmodified gum did not inhibit fungal growth. While, QAG inhibited the growth of most fungi used in this study. By AFM technique QAG interacted with the fungal surface, altering wall roughness significantly. The probable affinity of fragments of the QAG structure for the fungal enzyme 5I33 (Adenylosuccinate synthetase) has been shown by molecular docking. Low cytotoxicity was observed for polymers (unmodified gum and QAG). The results demonstrate that the quaternized polymer of AG presented in this study is a quite promising biomaterial for biotechnological applications.

Keywords: Antimicrobial; Biocompatibility; Chemically modified polymer.

MeSH terms

  • Animals
  • Antifungal Agents* / chemistry
  • Antifungal Agents* / pharmacology
  • Cytotoxins* / chemistry
  • Cytotoxins* / pharmacology
  • Enzyme Inhibitors* / chemistry
  • Enzyme Inhibitors* / pharmacology
  • Fabaceae / chemistry*
  • Fungal Proteins* / antagonists & inhibitors
  • Fungal Proteins* / chemistry
  • Fungi / enzymology*
  • HEK293 Cells
  • Humans
  • Ligases / antagonists & inhibitors
  • Ligases / chemistry
  • Mice
  • Molecular Docking Simulation*
  • Polysaccharides* / chemistry
  • Polysaccharides* / pharmacology

Substances

  • Antifungal Agents
  • Cytotoxins
  • Enzyme Inhibitors
  • Fungal Proteins
  • Polysaccharides
  • Ligases