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February 11, 2026Foods4 citationsOpen Access

Separation, Purification, Structural Characterization and Hypoglycemic Effect Study of Homogeneous Mori fructus Polysaccharide

QDQingfang DengYHYuanyuan HuangWXWen Xie

Key Points

  • This research aims to isolate and structurally characterize a homogeneous polysaccharide from Mori fructus, while evaluating its hypoglycemic effects.
  • Purification of MFP-III via DEAE-52 cellulose chromatography and Sephadex G-100 gel filtration.
  • Validation of purity using high-performance liquid chromatography (HPLC).
  • Analysis of structural characteristics using HPLC, GC-MS, FTIR, and NMR spectroscopy.
  • Evaluation of hypoglycemic activity against α-glucosidase and α-amylase.
  • MFP-III achieved 94.2% purity and had a molecular weight of approximately 6.83 kDa.
  • The polysaccharide is primarily composed of rhamnose, arabinose, galactose, glucose, mannose, and galacturonic acid.
  • MFP-III exhibited strong inhibitory activity against α-glucosidase (IC50 = 1.56 mg/mL) and α-amylase (IC50 = 2.07 mg/mL), outperforming acarbose at similar concentrations.

Abstract

Background/Objectives: Mori fructus polysaccharides are key bioactive components with diverse activities, but structural characterization of homogeneous fractions remains limited, hindering insights into structure–activity relationships. This study addresses this gap by isolating and characterizing a homogeneous polysaccharide (MFP-III) from M. fructus. Methods: MFP-III, representing the final gel-filtration homogeneous fraction, was purified using defined procedures: DEAE-52 cellulose chromatography followed by Sephadex G-100 gel filtration. Purity and homogeneity were validated by high-performance liquid chromatography (HPLC). Structural characteristics were analyzed via HPLC, GC-MS, FTIR, and NMR spectroscopy. Meanwhile, hypoglycemic activity of MFP-III was evaluated. Results: MFP-III (94.2 ± 2.6%) has a molecular weight of approximately 6.83 kDa, primarily composed of rhamnose, arabinose, galactose, glucose, mannose, and galacturonic acid. Its backbone structure is presumed to be →2,4)-α-L-Rhap-(1 → 4)-α-D-GalpA-(1→, with branching units potentially attached to O-4. MFP-III demonstrated significant inhibitory activity against α-glucosidase (IC50 = 1.56 mg/mL) and α-amylase (IC50 = 2.07 mg/mL), stronger than acarbose at equivalent concentrations. Conclusions: The findings provide preliminary insights into the hypoglycemic structure–activity relationship of MFP-III, providing data support for the development of blood glucose-lowering natural inhibitors, and offering a theoretical foundation for advancing the application of polysaccharides from other sources.

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Cite This Study

Deng et al. (2026) studied this question.

synapsesocial.com/papers/698c1c8e267fb587c655f0dahttps://doi.org/10.3390/foods15040629
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