4.8 Article

Class-A penicillin binding proteins do not contribute to cell shape but repair cell-wall defects

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ELIFE
卷 9, 期 -, 页码 -

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ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.51998

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  1. H2020 European Research Council [679980, 677823]
  2. Agence Nationale de la Recherche [ANR-10-LABX-62-IBEID]
  3. Volkswagen Foundation
  4. Knut och Alice Wallenbergs Stiftelse
  5. Swedish Research Council
  6. Kempe Foundations
  7. Laboratory for Molecular Infection Medicine Sweden
  8. European Research Council (ERC) [677823, 679980] Funding Source: European Research Council (ERC)

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Cell shape and cell-envelope integrity of bacteria are determined by the peptidoglycan cell wall. In rod-shaped Escherichia coli, two conserved sets of machinery are essential for cell-wall insertion in the cylindrical part of the cell: the Rod complex and the class-A penicillin-binding proteins (aPBPs). While the Rod complex governs rod-like cell shape, aPBP function is less well understood. aPBPs were previously hypothesized to either work in concert with the Rod complex or to independently repair cell-wall defects. First, we demonstrate through modulation of enzyme levels that aPBPs do not contribute to rod-like cell shape but are required for mechanical stability, supporting their independent activity. By combining measurements of cell-wall stiffness, cell-wall insertion, and PBP1b motion at the single-molecule level, we then present evidence that PBP1b, the major aPBP, contributes to cell-wall integrity by repairing cell wall defects.

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