Biological Engineering Program, College of Engineering, 4105 Old Main Hill, Utah State University, Logan, UT 84322-4105, USA.
Biopolymers. 2010 Feb;93(2):171-7. doi: 10.1002/bip.21315.
The structure of a bacterial cell wall may alter during bacterial reproduction. Moreover, these cell wall variations, on a nanoscale resolution, have not yet fully been elucidated. In this work, Raman spectroscopy and atomic force microscopy (AFM) technique are applied to evaluate the culture time-dependent cell wall structure variations of Pseudomonas putida KT2440 at a quorum and single cell level. The Raman spectra indicate that the appearance of DNA/RNA, protein, lipid, and carbohydrates occurs till 6 h of cultivation time under our experimental conditions. AFM characterization reveals the changes of the cellular surface ultrastructures over the culture time period, which is a gradual increase in surface roughness during the time between the first two and eight hours cultivation time. This work demonstrates the feasibility of utilizing a combined Raman spectroscopy and AFM technique to investigate the cultivation time dependence of bacterial cellular surface biopolymers at single cell level.
细菌细胞壁的结构可能会在细菌繁殖过程中发生改变。此外,这些细胞壁变化在纳米尺度分辨率下尚未完全阐明。在这项工作中,拉曼光谱和原子力显微镜(AFM)技术被应用于评估铜绿假单胞菌 KT2440 在群体和单细胞水平上与培养时间相关的细胞壁结构变化。拉曼光谱表明,在我们的实验条件下,培养 6 小时内会出现 DNA/RNA、蛋白质、脂质和碳水化合物。AFM 特性分析揭示了细胞表面超微结构随培养时间的变化,在最初的两个和八个小时的培养时间之间,表面粗糙度逐渐增加。这项工作证明了结合拉曼光谱和 AFM 技术在单细胞水平上研究细菌细胞表面生物聚合物培养时间依赖性的可行性。