# Metabolomics and Microbiomics Reveal the Cultivation-Dependent Divergence in Ginsenoside Biosynthesis and Rhizosphere Ecology of Panax ginseng

**Authors:** Siqi Liu, Dehua Wu, Wenqi Ma, Tielin Wang, Binbin Yan, Yang Ge, Feng Xiong, Hongyang Wang, Chuanzhi Kang

PMC · DOI: 10.3390/metabo16020138 · Metabolites · 2026-02-18

## TL;DR

This study shows that growing ginseng in a natural-like environment boosts its valuable ginsenoside content and supports a healthier soil microbiome compared to greenhouse cultivation.

## Contribution

The study reveals a microbiome-mediated mechanism linking cultivation environments to ginsenoside biosynthesis in Panax ginseng.

## Key findings

- Ginseng grown in simulative habitats has higher ginsenoside Re levels than greenhouse-grown ginseng.
- Bradyrhizobium and other microbes are enriched in simulative habitats and correlate with increased ginsenoside accumulation.
- Arched greenhouse cultivation leads to a more complex microbial structure with increased negative interactions.

## Abstract

Background: Cultivation environments impose distinct abiotic and biotic stresses that act as primary drivers reshaping the metabolic profile and microbiome assembly of medicinal plants. This study investigates the impact of simulative habitat versus arched greenhouse cultivation on the synthesis of bioactive ginsenosides and the associated root microbiome structure in Panax ginseng. Methods: A combined metabolomics and microbiomics approach was applied to compare ginsenoside accumulation and rhizosphere microbial community composition under the two cultivation modes. Results: Ginseng from simulative habitat cultivation exhibited significantly higher ginsenoside content, particularly ginsenoside Re, compared to arched greenhouse cultivation, with this advantage being more pronounced in long-term cultivation. Microbiome profiling revealed that specific taxa, including Bradyrhizobium, were strongly enriched in simulative habitats and positively correlated with enhanced ginsenoside accumulation, suggesting a microbiome-mediated mechanism for metabolic plasticity. In contrast, arched greenhouse cultivation was associated with a more complex microbial structure characterized by increased negative interactions, which may compromise metabolic quality. Conclusions: These findings, utilizing multi-omics correlations, provide a theoretical basis for optimizing Panax ginseng quality through ecological cultivation strategies that leverage stress-responsive microbe–metabolite interactions.

## Linked entities

- **Chemicals:** ginsenoside Re (PubChem CID 441921), ginsenosides (PubChem CID 3086007)
- **Species:** Panax ginseng (taxon 4054), Bradyrhizobium (taxon 374)

## Full-text entities

- **Diseases:** root rot (MESH:D005535), injury to (MESH:D014947), inflammatory (MESH:D007249), rusty root disease (MESH:D011843), borne diseases (MESH:D017282), weakness (MESH:D018908), cancer (MESH:D009369), spleen deficiency (MESH:D013160), soil (MESH:D005242), infections (MESH:D007239)
- **Chemicals:** iron (MESH:D007501), water (MESH:D014867), ethanol (MESH:D000431), formic acid (MESH:C030544), phosphate (MESH:D010710), Ginsenoside (MESH:D036145), methanol (MESH:D000432), acetonitrile (MESH:C032159), Re (MESH:D012211), carbon (MESH:D002244), ginsenoside Rg1 (MESH:C035054), nitrogen (MESH:D009584), agarose (MESH:D012685), ginsenoside Rb1 (MESH:C442759), ice (MESH:D007053), glycosides (MESH:D006027), IAA (-), triterpenoid (MESH:D014315), ginsenoside Re (MESH:C049864), sodium hypochlorite (MESH:D012973), nitrites (MESH:D009573)
- **Species:** Sphingomonas (genus) [taxon 13687], Fusarium cerealis (species) [taxon 56641], Terriglobales (Acidobacteria subdivision 1, order) [taxon 204433], Pseudomonadota (proteobacteria, phylum) [taxon 1224], Lechevalieria [taxon 166974], Paenibacillus (genus) [taxon 44249], Paraburkholderia (genus) [taxon 1822464], Pseudonocardia (genus) [taxon 1847], Panax ginseng (Asiatic ginseng, species) [taxon 4054], Actinomycetota (actinobacteria, phylum) [taxon 201174], Vibrio (genus) [taxon 662], Malus domestica (apple, species) [taxon 3750], Acidibacter (genus) [taxon 1549619], Mirabilis himalaica (species) [taxon 482968], Caballeronia (genus) [taxon 1827195], Pulsatilla tongkangensis (species) [taxon 1111685], Stenotrophomonas (genus) [taxon 40323], Fusarium (genus) [taxon 5506], Panax notoginseng (notoginseng, species) [taxon 44586], Rhodanobacter (genus) [taxon 75309], Gaiellales (order) [taxon 1154584], Pseudomonas (RNA similarity group I, genus) [taxon 286], Enterobacteriaceae (enterobacteria, family) [taxon 543], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Bradyrhizobium (genus) [taxon 374], Pararhizobium (genus) [taxon 1612611], Bacillus (genus) [taxon 55087], Microbacterium (genus) [taxon 33882], Ilyonectria robusta (species) [taxon 1079257], Dendrobium (genus) [taxon 37818], Mesorhizobium (genus) [taxon 68287], Rhizobium (genus) [taxon 379], Bacteroidota (Bacteroides-Cytophaga-Flexibacter group, phylum) [taxon 976], Sphingobium (genus) [taxon 165695], Acidobacteriota (phylum) [taxon 57723], Mycobacterium (genus) [taxon 1763], Neorhizobium (genus) [taxon 1525371], Matricaria chamomilla (species) [taxon 98504], Cylindrocarpon (genus) [taxon 13474], Burkholderia (genus) [taxon 32008], Homo sapiens (human, species) [taxon 9606], Delftia (genus) [taxon 80865], Panax quinquefolius (American ginseng, species) [taxon 44588], Gaiella (genus) [taxon 1154586], Amycolatopsis (genus) [taxon 1813], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]
- **Cell lines:** AG5 — Rattus norvegicus (Rat), Transformed cell line (CVCL_UG77), SH15 — Homo sapiens (Human), Neuroblastoma, Cancer cell line (CVCL_W974)

## Full text

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## Figures

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## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942689/full.md

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Source: https://tomesphere.com/paper/PMC12942689