# Silicate minerals enhance the expression of genes related to mineral dissolution by Priestia aryabhattai strain C4-10

**Authors:** Qi Sheng, Xin-Yi Zheng, Si-Han Yang, Wen Dong, Lin-Yan He, Xia-Fang Sheng

PMC · DOI: 10.1128/aem.02554-25 · Applied and Environmental Microbiology · 2026-01-26

## TL;DR

This study reveals how a specific bacteria strain dissolves silicate minerals by activating certain genes and metabolic pathways.

## Contribution

The study identifies specific genes and metabolic pathways activated in a gram-positive bacterium during silicate mineral dissolution.

## Key findings

- Priestia aryabhattai strain C4-10 increases Fe, Mg, and Si concentrations in media containing biotite or lizardite.
- Genes related to acid metabolism, biofilm formation, and transporters are upregulated during mineral dissolution.
- Strong correlations exist between gene expression and metal concentrations during mineral dissolution.

## Abstract

Silicate mineral-microbe interactions are essential for soil formation, element biogeochemical cycles, and carbon sequestration. However, the molecular mechanisms by which gram-positive bacteria mediate mineral dissolution remain largely unexplored. Here, we characterized a highly effective mineral-dissolving Priestia aryabhattai strain, C4-10, for its biotite and lizardite dissolution activity, alongside the underlying molecular mechanisms. In the medium supplemented with biotite or lizardite, C4-10 significantly increased the Fe, Mg, and Si concentrations between 4 and 48 h of incubation compared to the controls. Notably, in the C4-10-inoculated medium supplemented with biotite or lizardite, significantly decreased pH values in the medium and increased cell counts and biofilm formation on the mineral surfaces were observed over 24 h of incubation. A comparative transcriptomic analysis indicated that significantly upregulated differentially expressed genes were enriched in pathways related to glyoxylate and dicarboxylate metabolism, amino acid biosynthesis, the tricarboxylic acid cycle, and ABC transporters in the presence of biotite. Additionally, the gene expression of lutA_2 and actP associated with acid metabolism, glgC linked to biofilm formation, gtaB_3 related to cell wall components, and 02676, levE, and glnQ associated with transporters, was significantly upregulated in C4-10 in the presence of biotite or lizardite. Importantly, strong positive correlations were observed between the Fe or Mg concentrations and the relative expression levels of these genes during the biotite or lizardite dissolution process by C4-10. Our findings illustrate the involvement of multiple genes and metabolic pathways related to mineral dissolution, highlighting similar molecular mechanisms associated with both biotite and lizardite dissolution by C4-10.

To date, the molecular mechanisms underlying the dissolution of silicate minerals by gram-positive bacteria remain poorly understood. This study characterizes the mechanisms involved in biotite and lizardite dissolution by C4-10. C4-10 enhanced mineral dissolution through the production of organic acids, cell adsorption, and biofilm formation on mineral surfaces. The presence of biotite upregulated the expression of genes related to mineral dissolution and enriched metabolic pathways, including glyoxylate and dicarboxylate metabolism, amino acid biosynthesis, butanoate metabolism, the tricarboxylic acid cycle, and ABC transporters. Furthermore, significant correlations were observed between Fe or Mg concentrations in the medium and the expression levels of genes associated with acid metabolism, biofilm formation, cell wall metabolism, and transporters during the dissolution of biotite or lizardite by C4-10. Our results provide new insights into the interactions between silicate minerals and mineral-dissolving gram-positive bacteria, as well as the molecular mechanisms that facilitate in these processes.

## Linked entities

- **Genes:** actP (acetate transporter) [NCBI Gene 914281], glgC (glucose-1-phosphate adenyltransferase) [NCBI Gene 884264], levE (phosphotransferase system (PTS) fructose-specific enzyme IIB component) [NCBI Gene 937078], glnQ (ABC transporter ATP-binding protein) [NCBI Gene 884094]
- **Chemicals:** Fe (PubChem CID 23925), Mg (PubChem CID 888), Si (PubChem CID 5461123)
- **Species:** Priestia aryabhattai (taxon 412384)

## Full-text entities

- **Chemicals:** C4-10 (-), Silicate (MESH:D017640), biotite (MESH:C047410), Fe (MESH:D007501), glyoxylate (MESH:C031150), Mg (MESH:D008274), amino acid (MESH:D000596), lizardite (MESH:C046240), tricarboxylic acid (MESH:D014233), carbon (MESH:D002244), Si (MESH:D012825)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Caulobacter zeae (species) [taxon 2055137]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12915317/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12915317/full.md

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Source: https://tomesphere.com/paper/PMC12915317