Department of Physics and Astronomy, University of Sheffield, Sheffield S3 7RH, United Kingdom.
Department of Molecular Biology and Biotechnology, University of Sheffield, Sheffield S10 2TN, United Kingdom.
ACS Nano. 2021 Oct 26;15(10):16011-16018. doi: 10.1021/acsnano.1c04375. Epub 2021 Sep 17.
Understanding how bacteria grow and divide requires insight into both the molecular-level dynamics of ultrastructure and the chemistry of the constituent components. Atomic force microscopy (AFM) can provide near molecular resolution images of biological systems but typically provides limited chemical information. Conversely, while super-resolution optical microscopy allows localization of particular molecules and chemistries, information on the molecular context is difficult to obtain. Here, we combine these approaches into STORMForce (stochastic optical reconstruction with atomic force microscopy) and the complementary SIMForce (structured illumination with atomic force microscopy), to map the synthesis of the bacterial cell wall structural macromolecule, peptidoglycan, during growth and division in the rod-shaped bacterium . Using "clickable" d-amino acid incorporation, we fluorescently label and spatially localize a short and controlled period of peptidoglycan synthesis and correlate this information with high-resolution AFM of the resulting architecture. During division, septal synthesis occurs across its developing surface, suggesting a two-stage process with incorporation at the leading edge and with considerable in-filling behind. During growth, the elongation of the rod occurs through bands of synthesis, spaced by ∼300 nm, and corresponds to denser regions of the internal cell wall as revealed by AFM. Combining super-resolution optics and AFM can provide insights into the synthesis processes that produce the complex architectures of bacterial structural biopolymers.
了解细菌的生长和分裂需要深入了解超微结构的分子水平动态和组成成分的化学性质。原子力显微镜(AFM)可以提供生物系统的近分子分辨率图像,但通常提供有限的化学信息。相反,虽然超分辨率光学显微镜可以定位特定的分子和化学物质,但关于分子背景的信息很难获得。在这里,我们将这些方法结合到 STORMForce(原子力显微镜的随机光学重建)和互补的 SIMForce(原子力显微镜的结构照明)中,以绘制杆状细菌中细菌细胞壁结构大分子肽聚糖在生长和分裂过程中的合成图。使用“可点击”的 D-氨基酸掺入,我们荧光标记并空间定位短时间和受控的肽聚糖合成期,并将此信息与生成结构的高分辨率 AFM 相关联。在分裂过程中,隔室合成发生在其发育表面上,这表明存在一个两阶段过程,在前沿进行掺入,并且在后面有大量填充。在生长过程中,杆的伸长通过合成带发生,间隔约 300nm,与 AFM 揭示的内部细胞壁的密集区域相对应。将超分辨率光学和 AFM 结合起来,可以深入了解产生细菌结构生物聚合物复杂结构的合成过程。