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杆状细菌SBW25球形缺失突变体的进化拯救

Evolutionary rescue of spherical deletion mutants of the rod-shape bacterium SBW25.

作者信息

Yulo Paul Richard J, Desprat Nicolas, Gerth Monica L, Ritzl-Rinkenberger Barbara, Farr Andrew D, Liu Yunhao, Zhang Xue-Xian, Miller Michael, Cava Felipe, Rainey Paul B, Hendrickson Heather L

机构信息

Institute of Natural and Mathematical Science, Massey University, Auckland, New Zealand.

Laboratoire de Physique de l'ENS, Université Paris Cité, Ecole normale supérieure, UniversitéPSL, Sorbonne Université, CNRS, 75005 Paris, Paris, France.

出版信息

Elife. 2025 Mar 31;13:RP98218. doi: 10.7554/eLife.98218.

Abstract

Maintenance of rod-shape in bacterial cells depends on the actin-like protein MreB. Deletion of from SBW25 results in viable spherical cells of variable volume and reduced fitness. Using a combination of time-resolved microscopy and biochemical assay of peptidoglycan synthesis, we show that reduced fitness is a consequence of perturbed cell size homeostasis that arises primarily from differential growth of daughter cells. A 1000-generation selection experiment resulted in rapid restoration of fitness with derived cells retaining spherical shape. Mutations in the peptidoglycan synthesis protein Pbp1A were identified as the main route for evolutionary rescue with genetic reconstructions demonstrating causality. Compensatory mutations that targeted transpeptidase activity enhanced homogeneity of cell wall synthesis on lateral surfaces and restored cell size homeostasis. Mechanistic explanations require enhanced understanding of why deletion of causes heterogeneity in cell wall synthesis. We conclude by presenting two testable hypotheses, one of which posits that heterogeneity stems from non-functional cell wall synthesis machinery, while the second posits that the machinery is functional, albeit stalled. Overall, our data provide support for the second hypothesis and draw attention to the importance of balance between transpeptidase and glycosyltransferase functions of peptidoglycan building enzymes for cell shape determination.

摘要

细菌细胞杆状形态的维持依赖于肌动蛋白样蛋白MreB。从SBW25中缺失MreB会导致产生体积可变且适应性降低的存活球形细胞。通过结合时间分辨显微镜和肽聚糖合成的生化分析,我们表明适应性降低是细胞大小稳态受到干扰的结果,这种干扰主要源于子细胞的差异生长。一项1000代的选择实验导致适应性迅速恢复,衍生细胞保持球形。肽聚糖合成蛋白Pbp1A中的突变被确定为进化拯救的主要途径,基因重建证明了因果关系。针对转肽酶活性的补偿性突变增强了细胞壁在侧面合成的均匀性,并恢复了细胞大小稳态。要进行机制解释,需要更深入地了解为什么缺失MreB会导致细胞壁合成的异质性。我们通过提出两个可检验的假设来得出结论,其中一个假设认为异质性源于无功能的细胞壁合成机制,而另一个假设则认为该机制是有功能的,尽管处于停滞状态。总体而言,我们的数据为第二个假设提供了支持,并提请注意肽聚糖构建酶的转肽酶和糖基转移酶功能之间的平衡对于细胞形状确定的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8088/11957537/6576365f1f44/elife-98218-fig1.jpg

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