MurJ is the flippase of lipid-linked precursors for peptidoglycan biogenesis

Author:

Sham Lok-To1,Butler Emily K.2,Lebar Matthew D.3,Kahne Daniel34,Bernhardt Thomas G.1,Ruiz Natividad2

Affiliation:

1. Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA.

2. Department of Microbiology, Ohio State University, Columbus, OH 43210, USA.

3. Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA.

4. Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.

Abstract

Building the cell wall is flipping difficult The cell wall of bacteria is constructed from a polysaccharide called peptidoglycan (PG). It forms a matrix that surrounds cells and is essential for the integrity of the cytoplasmic membrane. Many of our most successful antibiotics target PG synthesis. The synthetic pathway involves the assembly of sugar building blocks on a lipid carrier at the inner face of the cytoplasmic membrane. The reactions that produce this so-called lipid II precursor and the enzymes that catalyze them have been known for decades. However, the identity of the flippase enzyme that “flips” lipid II in the membrane to expose the sugar building blocks on the cell surface for polymerization has remained highly controversial. Sham et al. now show that the essential protein MurJ is the long sought-after flippase responsible for the translocation of lipid-linked cell wall precursors across the bacterial cytoplasmic membrane (see the Perspective by Young). The work completes the cell wall biogenesis pathway and defines the function of an attractive target for new antibiotics. Science , this issue p. 220 ; see also p. 139

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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