# Aspergillus oryzae solid-state fermentation enriches protopanaxatriol-type ginsenosides in Panax ginseng and confers cytoprotective effects in vitro

**Authors:** Xinyang Li, Hu Ding, Ergang Wang, Shumin Wang, Huan Wang, Changbao Chen

PMC · DOI: 10.3389/fmicb.2026.1747324 · Frontiers in Microbiology · 2026-03-06

## TL;DR

A food-safe fermentation process using Aspergillus oryzae increases beneficial ginsenosides in ginseng and protects cells from damage.

## Contribution

A novel food-grade solid-state fermentation method to enrich cytoprotective ginsenosides in white ginseng.

## Key findings

- Optimal SSF conditions increased PPT-type ginsenosides Rf and PPT by 3.55-fold and 5.03-fold.
- Fermented extract showed anti-inflammatory, antioxidant, and anti-apoptotic effects in a cell injury model.
- The process is proposed to use A. oryzae glycosidase activity for ginsenoside remodeling.

## Abstract

This study established and optimized a food-grade solid-state fermentation (SSF) process using Aspergillus oryzae to biotransform ginsenosides in five-year-old white ginseng roots.

Through single-factor and orthogonal tests, optimal SSF conditions were identified. UPLC-QTOF-MS/MS analysis was used to characterize ginsenoside profile changes. In an ethanol-induced injury model using GES-1 gastric epithelial cells, the fermented extract was evaluated for cytoprotective effects.

Optimal SSF conditions were fermentation time of 8 days, inoculum size of 2.5%, and temperature of 28°C. UPLC-QTOF-MS/MS analysis revealed significant remodeling of protopanaxatriol (PPT)-type ginsenosides, with ginsenoside Rf and PPT increasing by 3.55-fold and 5.03-fold, respectively (p < 0.05). In the ethanol-induced injury model using GES-1 gastric epithelial cells, the fermented extract demonstrated dose-dependent anti-inflammatory, antioxidant, and anti-apoptotic effects without cytotoxicity. We hypothesize that the extracellular glycosidase activity of A. oryzae mediates the sequential deglycosylation leading to the observed PPT-type enrichment, although the specific enzymes involved require further identification. Overall, these results provide a proof-of-concept for a food-safe SSF platform tailored to whole white ginseng roots. This process effectively remodels the ginsenoside profile to enrich cytoprotective PPT-type compounds, supporting its potential for nutraceutical development.

## Linked entities

- **Chemicals:** ethanol (PubChem CID 702)
- **Species:** Aspergillus oryzae (taxon 5062), Panax ginseng (taxon 4054)

## Full-text entities

- **Diseases:** cytotoxicity (MESH:D064420), inflammatory (MESH:D007249)
- **Chemicals:** ginsenoside Rf (MESH:C055328), ethanol (MESH:D000431), ginsenoside (MESH:D036145), PPT (MESH:C081552)
- **Species:** Panax ginseng (Asiatic ginseng, species) [taxon 4054], Aspergillus oryzae (species) [taxon 5062]

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC13002569/full.md

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Source: https://tomesphere.com/paper/PMC13002569