α-Glucosidase inhibitors and phytotoxins from Streptomyces xanthophaeus

Nat Prod Res. 2017 Sep;31(17):2062-2066. doi: 10.1080/14786419.2016.1269100. Epub 2016 Dec 26.

Abstract

Twenty-four metabolites 1-24 were isolated from the fermentation broth of Streptomyces xanthophaeus. Their structures were elucidated on the basis of spectroscopic analysis and by comparison of their NMR data with literature data reported. Daidzein (1), genistein (2) and gliricidin (3) inhibited α-glucosidase in vitro with IC50 values of 174.2, 36.1 and 47.4 μM, respectively, more potent than the positive control, acarbose. Docking study revealed that the amino acid residue Thr 215 is the essential binding site for active ligands 2. In addition, the phytotoxic effects of all compounds were assayed on radish seedlings, five of which, 3, 8, 13, 15 and 18, inhibited the growth of radish (Raphanus sativus) seedlings with inhibitory rates of >60% at a concentration of 100 ppm, which was comparable or superior to the positive control glyphosate. This is the first report of the phytotoxicity of the compounds.

Keywords: 2,5-diketopiperazine; Streptomyces xanthophaeus; cyclodipeptide; herbicide; phytotoxins; α-glucosidase inhibitors.

MeSH terms

  • Acarbose / pharmacology
  • Binding Sites
  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical / methods
  • Glycoside Hydrolase Inhibitors / chemistry*
  • Glycoside Hydrolase Inhibitors / pharmacology*
  • Inhibitory Concentration 50
  • Magnetic Resonance Spectroscopy
  • Molecular Docking Simulation
  • Molecular Structure
  • Raphanus / drug effects
  • Raphanus / growth & development
  • Seedlings / drug effects
  • Streptomyces / chemistry*
  • Toxicity Tests / methods
  • alpha-Glucosidases / metabolism

Substances

  • Glycoside Hydrolase Inhibitors
  • alpha-Glucosidases
  • Acarbose