首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >In Vitro Cytotoxic Effects of Gold Nanoparticles Coated with Functional Acyl Homoserine Lactone Lactonase Protein from Bacillus licheniformis and Their Antibiofilm Activity against Proteus Species
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In Vitro Cytotoxic Effects of Gold Nanoparticles Coated with Functional Acyl Homoserine Lactone Lactonase Protein from Bacillus licheniformis and Their Antibiofilm Activity against Proteus Species

机译:地衣芽孢杆菌功能性酰基同型内酯内酯酶蛋白包被的金纳米粒子的体外细胞毒作用及其对变形杆菌物种的抗生物膜活性

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摘要

N-acylated homoserine lactonases are known to inhibit the signaling molecules of the biofilm-forming pathogens. In this study, gold nanoparticles were coated with N-acylated homoserine lactonase proteins (AiiA AuNPs) purified from Bacillus licheniformis. The AiiA AuNPs were characterized by UV-visible spectra, Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and X-ray diffraction (XRD). The synthesized AiiA AuNPs were found to be spherical in shape and 10 to 30 nm in size. Treatment with AiiA protein-coated AuNPs showed maximum reduction in exopolysaccharide production, metabolic activities, and cell surface hydrophobicity and potent antibiofilm activity against multidrug-resistant Proteus species compared to treatment with AiiA protein alone. AiiA AuNPs exhibited potent antibiofilm activity at 2 to 8 μM concentrations without being harmful to the macrophages. We conclude that at a specific dose, AuNPs coated with AiiA can kill bacteria without harming the host cells, thus representing a potential template for the design of novel antibiofilm and antibacterial protein drugs to decrease bacterial colonization and to overcome the problem of drug resistance. In summary, our data suggest that the combined effect of the lactonase and the gold nanoparticles of the AiiA AuNPs has promising antibiofilm activity against biofilm-forming and multidrug-resistant Proteus species.
机译:已知N-酰化的高丝氨酸内酰胺酶抑制形成生物膜的病原体的信号传导分子。在这项研究中,金纳米颗粒涂有从地衣芽孢杆菌纯化的N-酰化高丝氨酸内酯酶蛋白(AiiA AuNPs)。通过紫外可见光谱,傅立叶变换红外光谱(FTIR),透射电子显微镜(TEM)和X射线衍射(XRD)对AiiA AuNP进行了表征。发现合成的AiiA AuNP为球形,尺寸为10至30nm。与单独使用AiiA蛋白处理相比,用AiiA蛋白包被的AuNPs处理可最大程度降低胞外多糖的产生,代谢活性,细胞表面疏水性以及对多药耐药的变形杆菌的有效抗生物膜活性。 AiiA AuNPs在2至8μM浓度下显示出有效的抗生物膜活性,且对巨噬细胞无害。我们得出的结论是,在特定剂量下,涂有AiiA的AuNPs可以杀死细菌而不损害宿主细胞,因此代表了设计新型抗生物膜和抗菌蛋白药物以减少细菌定居并克服耐药性问题的潜在模板。总而言之,我们的数据表明,内酯酶和AiiA AuNPs的金纳米颗粒的联合作用具有针对生物膜形成和耐多药变形杆菌属物种的有希望的抗生物膜活性。

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