Stiff substrate increases mycelium growth rate on surface

Abstract Mycelium is crucial in decomposing biomass and cycling nutrients in nature. While various environmental factors can influence mycelium growth, the role of substrate mechanics is not yet clear. In this study, we investigate the effect of substrate stiffness on mycelium growth. We prepared agar substrates of different concentrations to grow the mycelium, but kept other environmental and chemical conditions consistent. We made a time-lapse recording of the growing history with minimum interruption. We repeated our tests for different species. Our results generally support that mycelium grows faster on a stiffer substrate, Ganoderma lucidum gives the highest growth rate and Pleurotus eryngii is most sensitive to substrate stiffness. We combined experimental characterization and computational simulation to investigate the mechanism and discovered that mycelium concentrates on the surface of a rigid substrate, but penetrates the soft one. Our Monte Carlo simulations illustrate that such a penetration allows mycelium to grow in the three-dimensional space, but effectively slows down the surface occupation speed. Our study provides insights into fungal growth and reveals that the mycelium growth rate can be tuned through substrate stiffness, thus reducing the time for producing mycelium-based composites. Impact statement We used agar substrates and tuned its stiffness to culture mycelium and compared tune its stiffness to culture mycelium and compare its growth in a well-controlled condition. Our results revealed that mycelium grows faster on stiffer substrates, thus fully occupying the petri dish surface more quickly. We repeated our study several times by testing four species, P. eryngii , G. lucidum , Trametes versicolor , and Flammulina velutipes, and the stiffest substrate always gives the highest mean growing rate than others. The G. lucidum shows the highest spreading rate that is obtained on the stiffest substrate as 39.1 ± 2.0 mm 2 /h. We found that the mycelium on a soft substrate will grow into the substrate instead of spreading on the stiffer surface. Our Monte Carlo simulations further show that once the fibers grow into a three-dimensional substrate, its growth is slower than growing on a two-dimensional surface, providing a microscopic mechanism of the substrate stiffness effect. This study’s analysis of how substrate stiffness impacts mycelium growth is new, bridging a critical knowledge gap in understanding the relationship between substrate mechanics and fungal ecology. The knowledge from this study has a potential in accelerating sustainable manufacturing of mycelium-based composite by adjusting substrate mechanics. Graphical Abstract

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Publication Details

Journal
MRS Bulletin
Published
2024-08-16
DOI
https://doi.org/10.1557/s43577-024-00762-1
Citations
9
Primary Topic
Plant and Biological Electrophysiology Studies
Type
article
Field-Weighted Citation Impact
5.40

Funders

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article

Stiff substrate increases mycelium growth rate on surface

Zhao Qin, Xiaoyue Hu, Libin Yang
9 citations
MRS Bulletin
Plant and Biological Electrophysiology Studies
5.40
article

Stiff substrate increases mycelium growth rate on surface

Zhao Qin, Xiaoyue Hu, Libin Yang
article en
9 citations

Abstract

Abstract Mycelium is crucial in decomposing biomass and cycling nutrients in nature. While various environmental factors can influence mycelium growth, the role of substrate mechanics is not yet clear. In this study, we investigate the effect of substrate stiffness on mycelium growth. We prepared agar substrates of different concentrations to grow the mycelium, but kept other environmental and chemical conditions consistent. We made a time-lapse recording of the growing history with minimum interruption. We repeated our tests for different species. Our results generally support that mycelium grows faster on a stiffer substrate, Ganoderma lucidum gives the highest growth rate and Pleurotus eryngii is most sensitive to substrate stiffness. We combined experimental characterization and computational simulation to investigate the mechanism and discovered that mycelium concentrates on the surface of a rigid substrate, but penetrates the soft one. Our Monte Carlo simulations illustrate that such a penetration allows mycelium to grow in the three-dimensional space, but effectively slows down the surface occupation speed. Our study provides insights into fungal growth and reveals that the mycelium growth rate can be tuned through substrate stiffness, thus reducing the time for producing mycelium-based composites. Impact statement We used agar substrates and tuned its stiffness to culture mycelium and compared tune its stiffness to culture mycelium and compare its growth in a well-controlled condition. Our results revealed that mycelium grows faster on stiffer substrates, thus fully occupying the petri dish surface more quickly. We repeated our study several times by testing four species, P. eryngii , G. lucidum , Trametes versicolor , and Flammulina velutipes, and the stiffest substrate always gives the highest mean growing rate than others. The G. lucidum shows the highest spreading rate that is obtained on the stiffest substrate as 39.1 ± 2.0 mm 2 /h. We found that the mycelium on a soft substrate will grow into the substrate instead of spreading on the stiffer surface. Our Monte Carlo simulations further show that once the fibers grow into a three-dimensional substrate, its growth is slower than growing on a two-dimensional surface, providing a microscopic mechanism of the substrate stiffness effect. This study’s analysis of how substrate stiffness impacts mycelium growth is new, bridging a critical knowledge gap in understanding the relationship between substrate mechanics and fungal ecology. The knowledge from this study has a potential in accelerating sustainable manufacturing of mycelium-based composite by adjusting substrate mechanics. Graphical Abstract

MRS BulletinVol. 49(12)
Syracuse University (US)
Directorate for Engineering
Life in Land
Openalex Percentile: Top 5%
Plant and Biological Electrophysiology Studies
5.40
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