Cell-Wall Recycling of the Gram-Negative Bacteria and the Nexus to Antibiotic Resistance

被引:164
作者
Dik, David A. [1 ]
Fisher, Jed F. [1 ]
Mobashery, Shahriar [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, McCourtney Hall, Notre Dame, IN 46556 USA
基金
美国国家卫生研究院;
关键词
PENICILLIN-BINDING PROTEINS; BETA-LACTAM RESISTANCE; DIAMINOPIMELATE DECARBOXYLASE SYNTHESIS; LYSR-TYPE REGULATOR; SYNERGISTIC TRANSCRIPTIONAL ACTIVATION; PSEUDOMONAS-AERUGINOSA-AMPR; 6-PHOSPHATE HYDROLASE MURQ; SMALL-MOLECULE INHIBITORS; X-RAY-STRUCTURE; ALA-D-ALA;
D O I
10.1021/acs.chemrev.8b00277
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The importance of the cell wall to the viability of the bacterium is underscored by the breadth of antibiotic structures that act by blocking key enzymes that are tasked with cell-wall creation, preservation, and regulation. The interplay between cell-wall integrity, and the summoning forth of resistance mechanisms to deactivate cell-wall-targeting antibiotics, involves exquisite orchestration among cell-wall synthesis and remodeling and the detection of and response to the antibiotics through modulation of gene regulation by specific effectors. Given the profound importance of antibiotics to the practice of medicine, the assertion that understanding this interplay is among the most fundamentally important questions in bacterial physiology is credible. The enigmatic regulation of the expression of the AmpC beta-lactamase, a clinically significant and highly regulated resistance response of certain Gram-negative bacteria to the beta-lactam antibiotics, is the exemplar of this challenge. This review gives a current perspective to this compelling, and still not fully solved, 35-year enigma.
引用
收藏
页码:5952 / 5984
页数:33
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