Faculty of Physics and Center for Nanoscience, Ludwig Maximilian University, Munich, Germany.
Max Planck Institute of Biochemistry, Martinsried, Germany.
Sci Adv. 2024 Jan 12;10(2):eadk5847. doi: 10.1126/sciadv.adk5847. Epub 2024 Jan 10.
Spore-forming bacteria have two distinct division modes: sporulation and vegetative division. The placement of the foundational division machinery component (Z-ring) within the division plane is contingent on the division mode. However, investigating if and how division is performed differently between sporulating and vegetative cells remains challenging, particularly at the nanoscale. Here, we use DNA-PAINT super-resolution microscopy to compare the 3D assembly and distribution patterns of key division proteins SepF, ZapA, DivIVA, and FtsZ. We determine that ZapA and SepF placement within the division plane mimics that of the Z-ring in vegetative and sporulating cells. We find that DivIVA assemblies differ between vegetative and sporulating cells. Furthermore, we reveal that SepF assembles into ~50-nm arcs independent of division mode. We propose a nanoscale model in which symmetric or asymmetric placement of the Z-ring and early divisome proteins is a defining characteristic of vegetative or sporulating cells, respectively, and regulation of septal thickness differs between division modes.
芽孢形成和营养分裂。基础分裂机制组件(Z 环)在分裂平面中的位置取决于分裂模式。然而,研究在芽孢形成和营养细胞之间是否以及如何以不同的方式进行分裂仍然具有挑战性,特别是在纳米尺度上。在这里,我们使用 DNA-PAINT 超分辨率显微镜来比较关键分裂蛋白 SepF、ZapA、DivIVA 和 FtsZ 的 3D 组装和分布模式。我们确定了 ZapA 和 SepF 在分裂平面中的位置类似于营养和芽孢形成细胞中 Z 环的位置。我们发现 DivIVA 组装在营养和芽孢形成细胞之间存在差异。此外,我们揭示了 SepF 形成独立于分裂模式的~50nm 弧。我们提出了一个纳米尺度模型,其中 Z 环和早期分裂体蛋白的对称或不对称放置分别是营养或芽孢形成细胞的特征,并且分裂模式之间的隔膜厚度调节不同。