Characterization, in vitro binding properties, and inhibitory activity on pancreatic lipase of β-glucans from different Qingke (Tibetan hulless barley) cultivars

Int J Biol Macromol. 2018 Dec;120(Pt B):2517-2522. doi: 10.1016/j.ijbiomac.2018.09.023. Epub 2018 Sep 5.

Abstract

In order to explore Qingke β-glucans as functional food ingredients for prevention of obesity, the physicochemical structures, in vitro binding properties, and inhibitory activities on pancreatic lipase of β-glucans from three different Qingke cultivars, including Ganyucang (black), Dingqing (blue), and Zangqing 320 (white), were investigated and compared. Results showed that molecular weights, particle sizes, and intrinsic viscosities of β-glucans from colored (black and blue) Qingke cultivars were much higher than those of white Qingke β-glucans, respectively. In addition, the constituent monosaccharides of β-glucans from colored Qingke cultivars were determined as arabinose, xylose, glucose, and galactose, and glucose was the dominant monosaccharide. Furthermore, colored Qingke β-glucans exerted strong fat binding, cholesterol binding, and bile-acid binding capacities, as well as inhibitory activities on pancreatic lipase, which were much higher than those of white Qingke β-glucans. Indeed, the fat binding, cholesterol binding, and bile-acid binding capacities, as well as the inhibitory activities on pancreatic lipase of Qingke β-glucans were positively associated with their molecular weights and intrinsic viscosities. Results are beneficial for better understanding of the structure-function relationship of Qingke β-glucans, and β-glucans from colored Qingke cultivars (Ganyucang and Dingqing) could be further explored as functional food ingredients for prevention of obesity.

Keywords: Binding property; Intrinsic viscosity; Molecular weights; Pancreatic lipase inhibition; Qingke; β-Glucans.

MeSH terms

  • Enzyme Inhibitors / metabolism*
  • Enzyme Inhibitors / pharmacology*
  • Hordeum / chemistry*
  • Lipase / antagonists & inhibitors*
  • Lipase / metabolism*
  • Molecular Weight
  • Protein Binding
  • Species Specificity
  • beta-Glucans / metabolism*
  • beta-Glucans / pharmacology*

Substances

  • Enzyme Inhibitors
  • beta-Glucans
  • Lipase