Kelsey Gray, Harley Edwards, Alexander G. Doan, Walker Huso, JungHun Lee, Wanwei Pan, Nelanne Bolima, Isha Gautam, Tuo Wang, Ranjan Srivastava, Marc Zupan, Mark R. Marten, Steven D. Harris
{"title":"The Impact of Fungal Developmental Structures on Mechanical Properties of Mycelial Materials","authors":"Kelsey Gray, Harley Edwards, Alexander G. Doan, Walker Huso, JungHun Lee, Wanwei Pan, Nelanne Bolima, Isha Gautam, Tuo Wang, Ranjan Srivastava, Marc Zupan, Mark R. Marten, Steven D. Harris","doi":"10.1002/elsc.70066","DOIUrl":null,"url":null,"abstract":"<p>This study explores how suppressing asexual development in <i>Aspergillus nidulans</i> enhances the mechanical properties of mycelial materials. Using four aconidial mutants <i>(∆brlA</i>, <i>∆flbA</i>, <i>∆fluG</i>, and <i>fadA<sup>G42R</sup></i>) lacking 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 <i>∆fluG</i> and <i>∆brlA</i> (fluffy nonsporulating, FNS phenotype) showing the highest UTS. Additionally, <i>fadA<sup>G42R</sup></i> and <i>∆flbA</i> (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 suggests that autolysis in FAD mutants may disrupt galactofuranose-related processes, altering cell wall composition and contributing to higher elasticity. These findings suggest suppression of asexual development increases 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.</p>","PeriodicalId":11678,"journal":{"name":"Engineering in Life Sciences","volume":"26 2","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2026-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12930277/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Engineering in Life Sciences","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/elsc.70066","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
This study explores how suppressing asexual development in Aspergillus nidulans enhances the mechanical properties of mycelial materials. Using four aconidial mutants (∆brlA, ∆flbA, ∆fluG, and fadAG42R) lacking 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 ∆fluG and ∆brlA (fluffy nonsporulating, FNS phenotype) showing the highest UTS. Additionally, fadAG42R and ∆flbA (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 suggests that autolysis in FAD mutants may disrupt galactofuranose-related processes, altering cell wall composition and contributing to higher elasticity. These findings suggest suppression of asexual development increases 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.
期刊介绍:
Engineering in Life Sciences (ELS) focuses on engineering principles and innovations in life sciences and biotechnology. Life sciences and biotechnology covered in ELS encompass the use of biomolecules (e.g. proteins/enzymes), cells (microbial, plant and mammalian origins) and biomaterials for biosynthesis, biotransformation, cell-based treatment and bio-based solutions in industrial and pharmaceutical biotechnologies as well as in biomedicine. ELS especially aims to promote interdisciplinary collaborations among biologists, biotechnologists and engineers for quantitative understanding and holistic engineering (design-built-test) of biological parts and processes in the different application areas.