# Structural Identification of Physalis alkekengi L. Polysaccharides

**Authors:** Yun Zhang, Xuan Wen, Neng Xu, Hongyan Fu, Ge Lv, Wenjie Yu, Lina Wei, Lin Zhao

PMC · DOI: 10.3390/molecules30040949 · Molecules · 2025-02-18

## TL;DR

This study identifies the structure of specific polysaccharides from Physalis alkekengi fruit, which may help improve their use in health and food industries.

## Contribution

The paper provides a detailed structural analysis of three novel polysaccharides from Physalis alkekengi.

## Key findings

- Phy-1b and Phy-1c polysaccharides have distinct sugar compositions and molar ratios.
- The main and branched chain structures of Phy-1b were determined using methylation and NMR analysis.
- The polysaccharides are neutral, lacking uronic acid, and have potential for high-value processing.

## Abstract

Physalis alkekengi L. fruit polysaccharides can reduce blood sugar, regulate blood lipids, and improve intestinal flora structure. However, the specific polysaccharide components exerting these effects are unclear. In this study, we extracted, separated, purified, and characterized the P. alkekengi polysaccharides Phy-1a, Phy-1b, and Phy-1c. Ion chromatography showed that Phy-1b was mainly composed of rhamnose, arabinose, galactose, glucose, and xylose at a molar ratio of 3.0:19.8:47.5:20.9:8.8, and Phy-1c was composed of rhamnose, arabinose, galactose, glucose, xylose, mannose, ribose Galactosamine hydrochloride and Glucosamine hydrochloride at a molar ratio of 10.4:7.9:22.8:30.5:4.6:4.4:19.4:3.9:5.8. Neither of these polysaccharides contained uronic acid, indicating their neutral property. Methylation analysis and nuclear magnetic resonance spectroscopy showed that Phy-1b was mainly composed of terminal sugars (1-Araf); 1,5-Araf; 1,4-Xylp; 1-Glcp; 2,4-Rhap; 1,3-Glcp; 1,4-Galp; 1,4-Glcp; 1,3-Galp; 1,6-Glcp; 1,3,6-Glcp; and 1,4,6-Galp at a molar ratio of 5.2:7.1:7.8:13.7:6.3:11.2:7.0:16.3:7.4:6.0:6.8:5.3, with the main chain being →2)-α-L-Rhap-(1→4)-β-d-Galp-(1→4)-β-d-Galp-(1→[3)-β-d-Glcp-(1]2→3)-β-d-Glcp-(1→[4)-β-d-Glcp-(1]2→ and the branched chains being β-L-Araf-(1→5)-β-L-Araf-(1→, β-d-Glcp-(1→4)-β-d-Xylp-(1→ 3)-β-d-Galp-(1→, and β-d-Glcp-(1→6)-β-d-Glcp-(1→. The three fragments, respectively, pass through the O-4 key of →2,4)-α-l-Rhap-(1→, O-6 key of →4,6)-β-d-Galp-(1→, and O-6 of →3,6)-β-d-Glcp-(1→ connected to the main chain. These results provide a reference for enhancing the utilization value of P. alkekengi resources to promote its high-value and efficient processing.

## Linked entities

- **Chemicals:** rhamnose (PubChem CID 25310), arabinose (PubChem CID 229), galactose (PubChem CID 6036), glucose (PubChem CID 5793), xylose (PubChem CID 135191), mannose (PubChem CID 18950), ribose (PubChem CID 10975657), Galactosamine hydrochloride (PubChem CID 74493), Glucosamine hydrochloride (PubChem CID 91431)

## Full-text entities

- **Chemicals:** glucose (MESH:D005947), galactose (MESH:D005690), uronic acid (MESH:D014574), xylose (MESH:D014994), 1,3-Glcp (-), mannose (MESH:D008358), Polysaccharides (MESH:D011134), arabinose (MESH:D001089), blood sugar (MESH:D001786), rhamnose (MESH:D012210), lipids (MESH:D008055), sugars (MESH:D000073893)
- **Species:** Alkekengi officinarum (Chinese-lantern, species) [taxon 33120]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11858199/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC11858199/full.md

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Source: https://tomesphere.com/paper/PMC11858199