Centre for Biospectroscopy and School of Chemistry, Monash University, Clayton Campus, Melbourne, 3800 Victoria, Australia.
Infection and Immunity Program, Monash Biomedicine Discovery Institute and Department of Microbiology, Monash University, Clayton Campus, Melbourne, 3800 Victoria, Australia.
J R Soc Interface. 2018 Mar;15(140). doi: 10.1098/rsif.2018.0115.
A new experimental platform for probing nanoscale molecular changes in living bacteria using atomic force microscopy-infrared (AFM-IR) spectroscopy is demonstrated. This near-field technique is eminently suited to the study of single bacterial cells. Here, we report its application to monitor dynamical changes occurring in the cell wall during cell division in using AFM to demonstrate the division of the cell and AFM-IR to record spectra showing the thickening of the septum This work was followed by an investigation into single cells, with particular emphasis on cell-wall signatures, in several bacterial species. Specifically, mainly cell wall components from and containing complex carbohydrate and phosphodiester groups, including peptidoglycans and teichoic acid, could be identified and mapped at nanometre spatial resolution. Principal component analysis of AFM-IR spectra of six living bacterial species enabled the discrimination of Gram-positive from Gram-negative bacteria based on spectral bands originating mainly from the cell wall components. The ability to monitor molecular changes during cellular processes in bacteria at the nanoscale opens a new platform to study environmental influences and other factors that affect bacterial chemistry.
本文展示了一种使用原子力显微镜-红外(AFM-IR)光谱法探测活细菌中纳米级分子变化的新型实验平台。这种近场技术非常适合研究单个细菌细胞。在这里,我们报告了它在使用 AFM 监测 细胞分裂过程中细胞壁动态变化方面的应用,并使用 AFM-IR 记录显示隔膜增厚的光谱。随后,我们对几种细菌的单细胞进行了研究,特别强调细胞壁特征。具体来说,能够以纳米级空间分辨率识别和绘制 和 中的主要细胞壁成分,包括肽聚糖和磷壁酸,这些成分含有复杂的碳水化合物和磷酸二酯基团。对六种活细菌的 AFM-IR 光谱进行主成分分析,能够根据主要源自细胞壁成分的光谱带区分革兰氏阳性菌和革兰氏阴性菌。在纳米尺度上监测细菌细胞过程中 分子变化的能力为研究环境影响和其他影响细菌化学的因素开辟了一个新的平台。