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Photomodulation of bacterial growth and biofilm formation using carbohydrate-based surfactants

机译:使用基于碳水化合物的表面活性剂对细菌生长和生物膜形成进行光调制

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摘要

Naturally occurring and synthetic carbohydrate amphiphiles have emerged as a promising class of antimicrobial and antiadhesive agents that act through a number of dynamic and often poorly understood mechanisms. In this paper, we provide the first report on the application of azobenzene trans-cis photoisomerization for effecting spatial and temporal control over bacterial growth and biofilm formation using carbohydrate-based surfactants. Photocontrollable surface tension studies and small angle neutron scattering (SANS) revealed the diverse geometries and dimensions of self-assemblies (micelles) made possible through variation of the head group and UV-visible light irradiation. Using these light-addressable amphiphiles, we demonstrate optical control over the antibacterial activity and formation of biofilms against multi-drug resistant (MDR) Pseudomonas aeruginosa, methicillin-resistant Staphylococcus aureus (MRSA) and Gram-negative Escherichia coli. To probe the mechanism of bioactivity further, we evaluated the impact of trans-cis photoisomerization in these surfactants on bacterial motility and revealed photomodulated enhancement in swarming motility in P. aeruginosa. These light-responsive amphiphiles should attract significant interest as a new class of antibacterial agents and as investigational tools for probing the complex mechanisms underpinning bacterial adhesion and biofilm formation.
机译:天然存在的和合成的碳水化合物两亲物已经成为一类有前途的抗微生物剂和抗粘剂,它们通过许多动态的且常常为人们所知的机制起作用。在本文中,我们提供了第一个关于偶氮苯反式顺式光异构化在使用碳水化合物基表面活性剂实现细菌生长和生物膜形成的时空控制方面的应用的报道。光控表面张力研究和小角度中子散射(SANS)表明,通过改变头组和紫外线可见光照射,可以实现多种多样的几何形状和自组装体(胶束)尺寸。使用这些光寻址的两亲物,我们证明了对多药抗性(MDR)铜绿假单胞菌,耐甲氧西林金黄色葡萄球菌(MRSA)和革兰氏阴性大肠杆菌的抗菌活性和生物膜形成的光学控制。为了进一步探究生物活性的机制,我们评估了这些表面活性剂中反式顺式光异构化对细菌运动的影响,并揭示了铜绿假单胞菌群运动中的光调节增强。这些对光敏感的两亲物应作为一类新型的抗菌剂和探索基础细菌粘附和生物膜形成的复杂机制的研究工具而引起人们的极大兴趣。

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