Literature DB >> 30195000

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

Huan Guo1, Shang Lin1, Min Lu1, Jia Duo Bu Gong2, Lu Wang2, Qing Zhang1, De-Rong Lin1, Wen Qin3, Ding-Tao Wu4.   

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.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

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

Mesh:

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Year:  2018        PMID: 30195000     DOI: 10.1016/j.ijbiomac.2018.09.023

Source DB:  PubMed          Journal:  Int J Biol Macromol        ISSN: 0141-8130            Impact factor:   6.953


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