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通过微流控模具的双光子聚合实现的真菌菌丝高度平行弯曲测试。

Highly parallel bending tests for fungal hyphae enabled by two-photon polymerization of microfluidic mold.

作者信息

Brinkmann Steffen, Schrader Marcel, Meinen Sven, Kampen Ingo, Kwade Arno, Dietzel Andreas

机构信息

Institute of Particle Technology, Technische Universität Braunschweig, Braunschweig, Germany.

Institute of Microtechnology, Technische Universität Braunschweig, Braunschweig, Germany.

出版信息

Front Bioeng Biotechnol. 2024 Nov 1;12:1449167. doi: 10.3389/fbioe.2024.1449167. eCollection 2024.

DOI:10.3389/fbioe.2024.1449167
PMID:39553394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11563782/
Abstract

Filamentous microorganisms exhibit a complex macro-morphology constituted of branched and cross-linked hyphae. Fully resolved mechanical models of such mycelial compounds rely heavily on accurate input data for mechanical properties of individual hyphae. Due to their irregular shape and high adaptability to environmental factors, the measurement of these intrinsic properties remains challenging. To overcome previous shortcomings of microfluidic bending tests, a novel system for the precise measurement of the individual bending stiffness of fungal hyphae is presented in this study. Utilizing two-photon polymerization, microfluidic molds were fabricated with a multi-material approach, enabling the creation of 3D cell traps for spore immobilization. Unlike previous works applying the methodology of microfluidic bending tests, the hyphae were deflected in the vertical center of the microfluidic channel, eliminating the adverse influence of nearby walls on measurements. This lead to a significant increase in measurement yield compared to the conventional design. The accuracy and reproducibility of bending tests was ensured through validation of the measurement flow using micro-particle image velocimetry. Our results revealed that the bending stiffness of hyphae of is approximately three to four times higher than that reported for hyphae. At the same time, the derived longitudinal Young's Modulus of the hyphal cell wall yields a comparable value for both organisms. The methodology established in this study provides a powerful tool for studying the effects of cultivation conditions on the intrinsic mechanical properties of single hyphae. Applying the results to resolved numerical models of mycelial compounds promises to shed light on their response to hydrodynamic stresses in biotechnological cultivation, which influences their expressed macro-morphology and in turn, product yields.

摘要

丝状微生物呈现出由分支和交联菌丝构成的复杂宏观形态。此类菌丝体化合物的完全解析力学模型在很大程度上依赖于单个菌丝力学性能的准确输入数据。由于其形状不规则且对环境因素适应性强,这些内在特性的测量仍然具有挑战性。为克服微流控弯曲测试先前的缺点,本研究提出了一种用于精确测量真菌菌丝单个弯曲刚度的新型系统。利用双光子聚合,采用多材料方法制造微流控模具,能够创建用于孢子固定的三维细胞陷阱。与先前应用微流控弯曲测试方法的工作不同,菌丝在微流控通道的垂直中心处发生偏转,消除了附近壁对测量的不利影响。与传统设计相比,这导致测量成功率显著提高。通过使用微粒子图像测速技术对测量流程进行验证,确保了弯曲测试的准确性和可重复性。我们的结果表明,[具体菌种1]菌丝的弯曲刚度比报道的[具体菌种2]菌丝大约高三到四倍。同时,推导出的菌丝细胞壁纵向杨氏模量在两种生物体中产生了可比的值。本研究建立的方法为研究培养条件对单个菌丝内在力学性能的影响提供了一个强大的工具。将结果应用于已解析的菌丝体化合物数值模型有望揭示它们在生物技术培养中对流体动力应力的响应,这会影响它们所呈现的宏观形态,进而影响产品产量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/9150ca6909c0/fbioe-12-1449167-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/d12fed12ab12/fbioe-12-1449167-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/d52a46e71b6f/fbioe-12-1449167-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/bb9d0d9da78a/fbioe-12-1449167-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/402d1fc3ca0e/fbioe-12-1449167-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/9722b87a5020/fbioe-12-1449167-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/21ce8efbe064/fbioe-12-1449167-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/9970d7397091/fbioe-12-1449167-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/4bbb033579a3/fbioe-12-1449167-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/9150ca6909c0/fbioe-12-1449167-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/d12fed12ab12/fbioe-12-1449167-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/d52a46e71b6f/fbioe-12-1449167-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/bb9d0d9da78a/fbioe-12-1449167-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/402d1fc3ca0e/fbioe-12-1449167-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/9722b87a5020/fbioe-12-1449167-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/21ce8efbe064/fbioe-12-1449167-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/9970d7397091/fbioe-12-1449167-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/4bbb033579a3/fbioe-12-1449167-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ce/11563782/9150ca6909c0/fbioe-12-1449167-g009.jpg

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