Institute of Enzymology, Research Centre for Natural Sciences, Budapest, Hungary.
Doctoral School of Biology and Institute of Biology, Eötvös Loránd University, Budapest, Hungary.
PLoS One. 2022 Feb 24;17(2):e0263975. doi: 10.1371/journal.pone.0263975. eCollection 2022.
The concerted action of DNA replication and cell division has been extensively investigated in eukaryotes. Well demarcated checkpoints have been identified in the cell cycle, which provides the correct DNA stoichiometry and appropriate growth in the progeny. In bacteria, which grow faster and less concerted than eukaryotes, the linkages between cell elongation and DNA synthesis are unclear. dTTP, one of the canonical nucleotide-building blocks of DNA, is also used for cell wall biosynthesis in mycobacteria. We hypothesize that the interconnection between DNA and cell wall biosynthesis through dTTP may require synchronization of these processes by regulating dTTP availability. We investigated growth, morphology, cellular dNTP pool, and possible signs of stress in Mycobacterium smegmatis upon perturbation of rhamnose biosynthesis by the overexpression of RmlA. RmlA is a cell wall synthetic enzyme that uses dTTP as the precursor for cross-linking the peptidoglycan with the arabinogalactan layers by a phosphodiester bond in the mycobacterial cell wall. We found that RmlA overexpression results in changes in cell morphology, causing cell elongation and disruption of the cylindrical cell shape. We also found that the cellular dTTP pool is reduced by half in RmlA overexpressing cells and that this reduced dTTP availability does not restrict cell growth. We observed 2-6-fold increases in the gene expression of replication and cell wall biosynthesis stress factors upon RmlA overexpression. Using super-resolution microscopy, we found that RmlA, acting to crosslink the nascent layers of the cell wall, localizes throughout the whole cell length in a helical pattern in addition to the cellular pole.
真核生物中广泛研究了 DNA 复制和细胞分裂的协同作用。细胞周期中已经确定了明确的检查点,这些检查点提供了正确的 DNA 化学计量和后代的适当生长。在比真核生物生长更快且协同性更低的细菌中,细胞伸长和 DNA 合成之间的联系尚不清楚。dTTP 是 DNA 的经典核苷酸构建块之一,也用于分枝杆菌的细胞壁生物合成。我们假设通过调节 dTTP 的可用性,DNA 和细胞壁生物合成之间的联系可能需要通过同步这些过程来实现。我们通过过表达 RmlA 来干扰鼠李糖的生物合成,研究了分枝杆菌生长、形态、细胞内 dNTP 池以及可能的应激迹象。RmlA 是一种细胞壁合成酶,它使用 dTTP 作为前体,通过磷酸二酯键将肽聚糖与阿拉伯半乳聚糖层交联,形成分枝杆菌细胞壁。我们发现 RmlA 的过表达导致细胞形态发生变化,导致细胞伸长和圆柱形细胞形状的破坏。我们还发现,RmlA 过表达细胞中的细胞内 dTTP 池减少了一半,而这种减少的 dTTP 可用性并不限制细胞生长。我们观察到,RmlA 过表达后,复制和细胞壁生物合成应激因子的基因表达增加了 2-6 倍。使用超分辨率显微镜,我们发现 RmlA 作为交联细胞壁新生层的作用,除了细胞极体外,还以螺旋模式定位于整个细胞长度。