Structural characterization and antioxidant activities of a water soluble polysaccharide isolated from Glycyrrhiza glabra

• Published in: International journal of biological macromolecules 2020-02, Vol.144, p.751-759
• Main Authors: Mutaillifu, Paiheerding, Bobakulov, Khayrulla, Abuduwaili, Aytursun, Huojiaaihemaiti, Haibaier, Nuerxiati, Rehebati, Aisa, Haji Akber, Yili, Abulimiti
• Format: Article
• Language: English
• Subjects: 1,4-Linked α-D-Glcp; Antioxidant activity; Glycyrrhiza glabra; Water soluble polysaccharide
• ISSN: 0141-8130; 1879-0003
• DOI: 10.1016/j.ijbiomac.2019.11.245

A water-soluble polysaccharide, named GPN, with molecular mass 38.7 kDa was isolated from Glycyrrhiza glabra with hot water extraction, ethanol precipitation, and purified by column chromatography. Monosaccharide composition analysis confirmed the presence of predominant glucose (98.03%) and trace amount of mannose, arabinose, and galactose. Methylation and GC–MS analysis revealed that the main glycosidic bonds in GPN comprised 1,4-linked Glcp, T-linked Glcp, 1,4,6-linked Glcp, and 1,6-linked Glcp. Based on these results and 1D/2D NMR spectroscopy, GPN has a linear backbone of 1,4-linked α-D-Glcp and 1,6-linked α-D-Glcp which substituted at C-4 of glucose. The side chain probably composed from 1,4-linked to main side α-D-Glcp and terminal 1-linked β-D-Glcp to the C-3 of D residue. Congo red assay confirmed the existence of triple helix structure. Moreover, SEM and XRD analysis revealed that the GPN had irregular fibrous, filaments like surface; and both crystalline and amorphous structure. GPN also displayed favorable thermal stability. Moreover, G.glabra polysaccharide showed good antioxidant activity. •A water soluble polysaccharide (GPN) was isolated and purified from Glycyrrhiza glabra.•GPN was a glucose predominant glucan like polysaccharide.•GPN was a repeating unit of 1,4-α-D-Glcp and 1,6-α-D-Glcp which substituted at C-4 of glucose.•Morphological features of GPN were determined by SEM, XRD.•The IC50 of crude polysaccharide on DPPH radical scavenging activity was 0.186 mg/mL.