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Bacterial cell-wall recycling.


ABSTRACT: Many Gram-negative and Gram-positive bacteria recycle a significant proportion of the peptidoglycan components of their cell walls during their growth and septation. In many--and quite possibly all--bacteria, the peptidoglycan fragments are recovered and recycled. Although cell-wall recycling is beneficial for the recovery of resources, it also serves as a mechanism to detect cell-wall-targeting antibiotics and to regulate resistance mechanisms. In several Gram-negative pathogens, anhydro-MurNAc-peptide cell-wall fragments regulate AmpC ?-lactamase induction. In some Gram-positive organisms, short peptides derived from the cell wall regulate the induction of both ?-lactamase and ?-lactam-resistant penicillin-binding proteins. The involvement of peptidoglycan recycling with resistance regulation suggests that inhibitors of the enzymes involved in the recycling might synergize with cell-wall-targeted antibiotics. Indeed, such inhibitors improve the potency of ?-lactams in vitro against inducible AmpC ?-lactamase-producing bacteria. We describe the key steps of cell-wall remodeling and recycling, the regulation of resistance mechanisms by cell-wall recycling, and recent advances toward the discovery of cell-wall-recycling inhibitors.

SUBMITTER: Johnson JW 

PROVIDER: S-EPMC3556187 | biostudies-literature | 2013 Jan

REPOSITORIES: biostudies-literature

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Bacterial cell-wall recycling.

Johnson Jarrod W JW   Fisher Jed F JF   Mobashery Shahriar S  

Annals of the New York Academy of Sciences 20121116


Many Gram-negative and Gram-positive bacteria recycle a significant proportion of the peptidoglycan components of their cell walls during their growth and septation. In many--and quite possibly all--bacteria, the peptidoglycan fragments are recovered and recycled. Although cell-wall recycling is beneficial for the recovery of resources, it also serves as a mechanism to detect cell-wall-targeting antibiotics and to regulate resistance mechanisms. In several Gram-negative pathogens, anhydro-MurNAc  ...[more]

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