Bacterial cell-wall recycling

被引:211
|
作者
Johnson, Jarrod W. [1 ]
Fisher, Jed F. [1 ]
Mobashery, Shahriar [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
关键词
AmpD; AmpG; AmpR; autolysin; BlaR1; Escherichia coli; lytic transglycosylase; MRSA; NagZ; PBP2a; Staphylococcus aureus; BETA-LACTAM RESISTANCE; N-ACETYLMURAMIC ACID; SOLUBLE LYTIC TRANSGLYCOSYLASE; PENICILLIN-BINDING PROTEINS; L-ALANINE AMIDASE; ESCHERICHIA-COLI; PSEUDOMONAS-AERUGINOSA; STAPHYLOCOCCUS-AUREUS; CRYSTAL-STRUCTURE; BLAR1; PROTEIN;
D O I
10.1111/j.1749-6632.2012.06813.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 beta-lactamase induction. In some Gram-positive organisms, short peptides derived from the cell wall regulate the induction of both beta-lactamase and beta-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 beta-lactams in vitro against inducible AmpC beta-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.
引用
收藏
页码:54 / 75
页数:22
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