Abstract
Understanding metabolic processes of soil fungi is essential for elucidating their ecological roles in biogeochemical cycles and responses to emergent environmental stressors. Here, we demonstrate the potential of using stable isotope probing Raman (SIP-Raman) microspectroscopy in microfluidics technology-based soil chips to trace glucose metabolism rates and stress responses in laboratory grown filamentous soil fungus Psilocybe cf. subviscida . The time evolution of Raman spectral band intensities resulting from deuterated glucose uptake in the fungal hyphae allowed us to assess glucose metabolism rates. Under excess copper (Cu) stress, we observed suppression of both glucose metabolic activity and growth. In addition, reduced spectral signatures of intracellular cytochrome c further implied impaired mitochondrial function and potential onset of cell death. However, laser-induced radiation damage hampered repeated Raman measurements, including multispectral mapping, on individual hyphae, especially when exposed to the Cu stress. To overcome this, we employed stimulated Raman scattering (SRS) microscopy, which offers much higher sensitivity and mapping speeds, and therefore much lower radiation doses. This enabled localization of the uptaken glucose at the inner edges of the P. cf. subviscida hyphae and Cu-induced formation of putative vacuolar structures. While integration of this approach with soil chips requires future modifications to the chip design for increased optical transparency and ensured sterility, overall, our results demonstrate the potential of Raman-based microspectroscopy for spatially resolved, in situ analysis of fungal primary metabolism and stress physiology.
| Original language | English |
|---|---|
| Article number | 101749 |
| Pages (from-to) | 1-10 |
| Number of pages | 10 |
| Journal | Fungal Biology |
| Volume | 130 |
| Issue number | 3 |
| Early online date | 13 Mar 2026 |
| DOIs | |
| Publication status | E-pub ahead of print - 13 Mar 2026 |
Bibliographical note
Publisher Copyright:© 2026 The Authors.
Funding
The authors acknowledge financial support from the Swedish Research Council to Milda Pucetaite (grant no 2021-03897 ) and the Foundation for Strategic Research to Edith Hammer (grant no. SSF FFL 18-0089 ). We further acknowledge financial support from NanoLund for fabrication of the microfluidic chip masters and from LaserLaB Europe ( EU Horizon 2020 grant # 871124 ) for supporting the SRS experiments at LaserLaB Amsterdam (access proposal ID: 26520). Thank you to Merel C. Konings for her help and support with operating the SRS system. The authors acknowledge financial support from the Swedish Research Council to Milda Pucetaite (grant no 2021-03897) and the Foundation for Strategic Research to Edith Hammer (grant no. SSF FFL 18-0089). We further acknowledge financial support from NanoLund for fabrication of the microfluidic chip masters and from LaserLaB Europe (EU Horizon 2020 grant # 871124) for supporting the SRS experiments at LaserLaB Amsterdam (access proposal ID: 26520). Thank you to Merel C. Konings for her help and support with operating the SRS system. Raman microspectroscopy measurements were performed at the Microscopy Facility at the Department of Biology, Lund University. Finally, Milda Pucetaite is grateful to prof. Toby Kiers and Dr. Vasilios Kokkoris at Vrije Universiteit Amsterdam for hosting her as a guest researcher during and beyond the course of this work. While preparing this manuscript, our co-author, colleague, and supervisor Freek Ariese sadly passed away. We acknowledge his invaluable contributions to this work in particular and to the scientific community at large. We are deeply grateful for his support, guidance, and friendship.
Keywords
- metabolic activity
- Microfluidic chips
- Raman scattering microspectroscopy
- Soil fungi
- Stable-isotope probing
- Stimulated Raman scattering (SRS) microscopy
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