The impact of fungal developmental structures on mechanical properties of mycelial materials

dc.contributor.authorGray, Kelsey
dc.contributor.authorEdwards, Harley
dc.contributor.authorDoan, Alexander G.
dc.contributor.authorHuso, Walker
dc.contributor.authorLee, JungHun
dc.contributor.authorPan, Wanwei
dc.contributor.authorBolima, Nelanne
dc.contributor.authorGautam, Isha
dc.contributor.authorWang, Tuo
dc.contributor.authorSrivastava, Ranjan
dc.contributor.authorZupan, Marc
dc.contributor.authorMarten, Mark
dc.contributor.authorHarris, Steven
dc.date.accessioned2025-07-09T17:55:20Z
dc.date.issued2025-4-1
dc.description.abstractThis study explores how suppressing asexual development in Aspergillus nidulans enhances the mechanical properties of mycelial materials. Using four aconidial mutants (ΔbrlA, ΔflbA, ΔfluG, and fadAᴳ⁴²ᴿ) that lack asexual development and a control strain (A28) that undergoes typical asexual development, we found that the absence of asexual development significantly improves mechanical strength. All mutants exhibited higher ultimate tensile strength (UTS) than the control, with ΔfluG and ΔbrlA (fluffy nonsporulating, FNS phenotype) showing the highest UTS. Additionally, fadAᴳ⁴²ᴿ and ΔflbA (fluffy autolytic dominant, FAD phenotype) demonstrated significantly higher strain at failure (SF), linked to increased autolysis and lower dry cell mass compared to the control and FNS mutants. Solid-state NMR analysis revealed that autolysis in FAD mutants disrupts galactofuranose-related metabolic processes, altering cell wall composition and contributing to higher elasticity. These findings suggest that suppressing asexual development enhances mycelial material strength, while autolysis mechanisms influence elasticity. This research highlights the potential for genetic manipulation in fungi to engineer advanced mycelial-based materials with tailored mechanical properties.
dc.description.sponsorshipStudent support for this work was provided by an NIGMS Initiative for Maximizing Student Development (IMSD) Grant (5 R25 GM055036), a NIGMS Graduate Research Training Initiative for Student Enhancement (G-RISE) Grant (T32-GM144876), G-RISE at UMBC awarded in 2021, National Science Foundation (NSF 2006189), and the Department of Defense (DoD) Science, Mathematics, and Research for Transformation (SMART) Scholarship - funded by the OUSD/R&E (The Under Secretary of Defense-Research and Engineering), and the National Defense Education Program (NDEP) / BA-1, Basic Research. Solid-state NMR analysis was supported by the National Institutes of Health (NIH) grant R01AI173270 to T.W.
dc.description.urihttps://www.biorxiv.org/content/10.1101/2025.04.01.644731v1
dc.format.extent16 pages
dc.genrejournal articles
dc.genrepreprints
dc.identifierdoi:10.13016/m23fdw-o23t
dc.identifier.urihttps://doi.org/10.1101/2025.04.01.644731
dc.identifier.urihttp://hdl.handle.net/11603/39301
dc.language.isoen_US
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Faculty Collection
dc.relation.ispartofUMBC Student Collection
dc.relation.ispartofUMBC Chemical, Biochemical & Environmental Engineering Department
dc.relation.ispartofUMBC Meyerhoff Scholars Program
dc.relation.ispartofUMBC Mechanical Engineering Department
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectUMBC MartenLab College of Engineering and Information Technology
dc.titleThe impact of fungal developmental structures on mechanical properties of mycelial materials
dc.typeText
dcterms.creatorhttps://orcid.org/0000-0003-4110-1687
dcterms.creatorhttps://orcid.org/0009-0008-6972-1865
dcterms.creatorhttps://orcid.org/0000-0002-1863-8956
dcterms.creatorhttps://orcid.org/0000-0003-2940-1476
dcterms.creatorhttps://orcid.org/0009-0002-7313-0255
dcterms.creatorhttps://orcid.org/0000-0003-1068-8470

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