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MreB Forms Subdiffraction Nanofilaments during Active Growth in Bacillus subtilis

机译:MreB在芽孢杆菌 枯草杆菌的主动生长过程中形成亚衍射纳米丝。

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The construction of the bacterial cell envelope is a fundamental topic, as it confers its integrity to bacteria and is consequently the target of numerous antibiotics. MreB is an essential protein suspected to regulate the cell wall synthetic machineries. Despite two decades of study, its localization remains the subject of controversies, its description ranging from helical filaments spanning the entire cell to small discrete entities. The true structure of these filaments is important because it impacts the model describing how the machineries building the cell wall are associated, how they are coordinated at the scale of the entire cell, and how MreB mediates this regulation. Our results shed light on this debate, revealing the size of native filaments in B. subtilis during growth. They argue against models where MreB filament size directly affects the speed of synthesis of the cell wall and where MreB would coordinate distant machineries along the side wall. ABSTRACT The actin-like MreB protein is a key player of the machinery controlling the elongation and maintenance of the cell shape of most rod-shaped bacteria. This protein is known to be highly dynamic, moving along the short axis of cells, presumably reflecting the movement of cell wall synthetic machineries during the enzymatic assembly of the peptidoglycan mesh. The ability of MreB proteins to form polymers is not debated, but their structure, length, and conditions of establishment have remained unclear and the subject of conflicting reports. Here we analyze various strains of Bacillus subtilis , the model for Gram-positive bacteria, and we show that MreB forms subdiffraction-limited, less than 200 nm-long nanofilaments on average during active growth, while micron-long filaments are a consequence of artificial overaccumulation of the protein. Our results also show the absence of impact of the size of the filaments on their speed, orientation, and other dynamic properties conferring a large tolerance to B. subtilis toward the levels and consequently the lengths of MreB polymers. Our data indicate that the density of mobile filaments remains constant in various strains regardless of their MreB levels, suggesting that another factor determines this constant.
机译:细菌细胞包膜的构建是一个基本主题,因为它赋予细菌以完整性,因此是众多抗生素的目标。 MreB是怀疑调节细胞壁合成机制的必需蛋白质。尽管进行了二十年的研究,但其定位仍然是争议的主题,其描述范围从横跨整个细胞的螺旋状细丝到小的离散实体。这些细丝的真实结构很重要,因为它会影响模型,该模型描述构建细胞壁的机械如何关联,它们如何在整个细胞范围内协调以及MreB如何介导这种调节。我们的结果揭示了这一争论,揭示了枯草芽孢杆菌生长过程中天然花丝的大小。他们反对模型,其中MreB细丝的大小直接影响细胞壁的合成速度,而MreB将协调沿侧壁的远距离机器。摘要肌动蛋白样MreB蛋白是控制大多数杆状细菌细胞形状的延长和维持的机制的关键参与者。已知该蛋白质是高度动态的,沿着细胞的短轴移动,大概反映了在肽聚糖网的酶促组装过程中细胞壁合成机制的运动。 MreB蛋白形成聚合物的能力尚无争议,但其结构,长度和建立条件仍不明确,且报告相互矛盾。在这里,我们分析了革兰氏阳性细菌模型的枯草芽孢杆菌的各种菌株,我们发现MreB在活跃的生长过程中形成亚衍射受限的平均长度小于200 nm的纳米丝,而微米长的细丝是人工合成的结果蛋白质的过度积累。我们的结果还表明,丝线的尺寸没有影响其速度,方向和其他动态特性,从而使枯草芽孢杆菌对MreB聚合物的含量和长度没有很大的耐受性。我们的数据表明,不管其MreB水平如何,可动丝的密度在各种菌株中均保持恒定,这表明另一个因素决定了该常数。

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