Klauer Ross R, Silvestri Rachel, White Hanna, Hayes Richard D, Riley Robert, Lipzen Anna, Barry Kerrie, Grigoriev Igor V, Talag Jayson, Bunting Victoria, Stevenson Zachary, Solomon Kevin V, Blenner Mark
Chemical and Biomolecular Engineering, University of Delaware, 150 Academy St., Newark, DE 19716.
U.S. Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA 94720.
bioRxiv. 2024 Nov 5:2024.11.05.622132. doi: 10.1101/2024.11.05.622132.
Microplastics present myriad ecological and human health risks including serving as a vector for pathogens in human and animal food chains. However, the specific mechanisms by which pathogenic fungi colonize these microplastics have yet to be explored. In this work, we examine the opportunistic fungal pathogen, and other common soil and marine , which we found bind microplastics tightly. Up to 3.85+/- 1.48 g microplastic plastic/g fungi were bound and flocculated for polypropylene (PP), polyethylene (PE), and polyethylene terephthalate (PET) powders and particles ranging in size from 0.05 - 5 mm. Gene knockouts revealed hydrophobins as a key biomolecule driving microplastic-fungi binding. Moreover, purified hydrophobins were still able to flocculate microplastics independent of the fungus. Our work elucidates a role for hydrophobins in fungal colonization of microplastics and highlights a potential target for mitigating the harm of microplastics through engineered fungal-microplastic interactions.
微塑料存在无数的生态和人类健康风险,包括作为人类和动物食物链中病原体的载体。然而,致病真菌在这些微塑料上定殖的具体机制尚未得到探索。在这项工作中,我们研究了机会性致病真菌以及其他常见的土壤和海洋真菌,我们发现它们能紧密结合微塑料。对于尺寸在0.05 - 5毫米范围内的聚丙烯(PP)、聚乙烯(PE)和聚对苯二甲酸乙二酯(PET)粉末及颗粒,每克真菌最多可结合并絮凝3.85±1.48克微塑料。基因敲除表明,疏水蛋白是驱动微塑料与真菌结合的关键生物分子。此外,纯化的疏水蛋白仍能独立于真菌使微塑料絮凝。我们的工作阐明了疏水蛋白在真菌定殖微塑料中的作用,并突出了通过工程化真菌与微塑料相互作用来减轻微塑料危害的潜在靶点。