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arXiv 2601.06754cond-mat.soft
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润湿耦合相分离作为活性细菌附着的能量机制

Wetting-coupled phase separation as an energetic mechanism for active bacterial adhesion

Advanced Materials Thrust, Function Hub, The Hong Kong University of Science and Technology (Guangzhou)(香港科技大学(广州)功能枢纽先进材料交叉中心);Institute of Chinese Medical Sciences & State Key Laboratory of Mechanism and Quality of Chinese Medicine, University of Macau(澳门大学中国医药研究国家重点实验室及中医药研究所);Department of Pharmaceutical Sciences, Faculty of Health Sciences, University of Macau(澳门大学健康科学学院药学系);Zhuhai UM Science and Technology Research Institute, University of Macau(澳门大学珠海科学技术研究院);Platform for Structure and Functional Technology of Neural Network, Guangdong Institute of Intelligence Science and Technology(广东省智能科学技术研究院神经网络结构与功能技术平台)

Dixi Yang, Anheng Wang, Jia Huang, Xiaofeng Zhuo, Chunming Wang, Hajime Tanaka, Jiaxing Yuan

AI总结:

本研究通过实验和模拟揭示了润湿耦合液-液相分离作为活性细菌附着能量机制的作用,阐明了细菌运动在不同相体积分数下的双重影响。

摘要:

运动细菌从稀释悬浮液中快速附着提出了一个根本的非平衡问题:流体动力学相互作用使细菌运动靠近表面而不产生稳定的约束,而静电相互作用主要是排斥性的。在这里,结合在聚乙烯醇/葡聚糖水两相系统中对铜绿假单胞菌和金黄色葡萄球菌的实验,以及大规模流体动力学模拟,我们识别出润湿耦合液-液相分离(LLPS)作为细菌附着的能量陷阱机制。当细菌进入优先润湿基底的相时,界面自由能最小化会创造一个深能量陷阱,稳定附着并通过毛细作用诱导横向聚类。关键的是,细菌运动发挥了双重作用:在低相体积分数时,活动增强了向润湿层的运输并促进积累,而在较高相体积时,通过自旋滴的形成抑制附着,通过产生对抗界面陷阱的流体动力学升力。我们的结果确立了润湿耦合LLPS作为指导活性悬浮液界面组织的通用物理途径。这为复杂流体中细菌附着提供了一个统一的能量框架,对解码细菌-细胞相互作用和控制生物膜形成具有广泛的意义。

英文摘要:

The rapid adhesion of motile bacteria from dilute suspensions poses a fundamental non-equilibrium problem: hydrodynamic interactions bias bacterial motion near surfaces without generating stable confinement, while electrostatic interactions are predominantly repulsive. Here, combining experiments on Pseudomonas aeruginosa and Staphylococcus aureus in a polyethylene glycol/dextran aqueous two-phase system with large-scale hydrodynamic simulations, we identify wetting-coupled liquid--liquid phase separation (LLPS) as an energetic trapping mechanism for bacterial adhesion. When bacteria partition into a phase that preferentially wets the substrate, interfacial free-energy minimization creates a deep energetic trap that stabilizes adhesion and induces lateral clustering via capillary interactions. Crucially, bacterial motility plays a dual role: at low phase volume fractions, activity enhances transport into the wetting layer and promotes accumulation, whereas at higher phase volumes it suppresses adhesion through the formation of self-spinning droplets that generate hydrodynamic lift opposing interfacial trapping. Our results establish wetting-coupled LLPS as a generic physical route governing interfacial organization in active suspensions. This provides a unified energetic framework for bacterial adhesion in complex fluids, with broad implications for deciphering bacterial-cell interactions and controlling biofilm formation.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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