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Regulation of peptidoglycan synthesis by outer-membrane proteins

机译:外膜蛋白对肽聚糖合成的调节

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摘要

Growth of the mesh-like peptidoglycan (PG) sacculus located between the bacterial inner and outer membranes (OM) is tightly regulated to ensure cellular integrity, maintain cell shape, and orchestrate division. Cytoskeletal elements direct placement and activity of PG synthases from inside the cell, but precise spatiotemporal control over this process is poorly understood. We demonstrate that PG synthases are also controlled from outside of the sacculus. Two OM lipoproteins, LpoA and LpoB, are essential for the function, respectively, of PBP1A and PBP1B, the major E. coli bifunctional PG synthases. Each Lpo protein binds specifically to its cognate PBP and stimulates its transpeptidase activity, thereby facilitating attachment of new PG to the sacculus. LpoB shows partial septal localization, and our data suggest that the LpoB-PBP1B complex contributes to OM constriction during cell division. LpoA/LpoB and their PBP-docking regions are restricted to γ-proteobacteria, providing models for niche-specific regulation of sacculus growth.
机译:紧密调节位于细菌内膜和外膜(OM)之间的网状肽聚糖(PG)囊的生长,以确保细胞完整性,维持细胞形状和协调分裂。细胞骨架元件从细胞内部指导PG合酶的放置和活性,但对该过程的精确时空控制了解甚少。我们证明PG合成酶也从囊外部被控制。两种OM脂蛋白LpoA和LpoB分别对主要的大肠杆菌双功能PG合酶PBP1A和PBP1B的功能至关重要。每个Lpo蛋白都与其结合的PBP特异性结合,并刺激其转肽酶活性,从而促进新的PG附着在眼囊上。 LpoB显示局部间隔定位,我们的数据表明LpoB-PBP1B复合物在细胞分裂过程中有助于OM收缩。 LpoA / LpoB及其PBP停靠区仅限于γ-变形细菌,从而为n的生境特定调节提供了模型。

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