Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Biomaterials. 2010 Oct;31(29):7526-33. doi: 10.1016/j.biomaterials.2010.06.032. Epub 2010 Jul 16.
The cellular responses of Escherichia coli to visible light photocatalysis were characterized by chemical, optical, electron-beam, and surface-force techniques, to elucidate the mechanisms of photocatalytic inactivation of E. coli on PdO/TiON fiber. The characterization techniques included chemical assays, fluorescence microscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and atomic force microscopy (AFM). Fluorescence microscopy using the Live/Dead BacLight kit indicates that the photocatalytic treatment resulted in severe membrane damage to the E. coli cells. SEM, AFM and TEM revealed drastic defects in the morphology and internal sub-structure of the bacterial cells after the treatments. Combining data from our previous reports on the antimicrobial properties of visible-light-activated PdO/TiON photocatalyst, the present results point to oxidative attack from the exterior to the interior of the bacteria by hydroxyl radicals as the primary mechanism of photocatalytic inactivation.
采用化学、光学、电子束和表面力技术对大肠杆菌对可见光光催化的细胞反应进行了表征,以阐明 PdO/TiON 纤维上光催化灭活大肠杆菌的机制。表征技术包括化学分析、荧光显微镜、扫描电子显微镜 (SEM)、透射电子显微镜 (TEM) 和原子力显微镜 (AFM)。使用 Live/Dead BacLight 试剂盒的荧光显微镜表明,光催化处理导致大肠杆菌细胞的严重膜损伤。SEM、AFM 和 TEM 显示处理后细菌细胞的形态和内部亚结构发生了剧烈的缺陷。结合我们之前关于可见光激活 PdO/TiON 光催化剂的抗菌性能的报告中的数据,目前的结果表明,由羟基自由基从外部到内部对细菌的氧化攻击是光催化灭活的主要机制。