Chemical genetic approaches for the discovery of bacterial cell wall inhibitors

被引:1
|
作者
Gupta, Rinki [1 ]
Singh, Mangal [1 ,2 ]
Pathania, Ranjana [1 ]
机构
[1] Indian Inst Technol Roorkee, Dept Biosci & Bioengn, Roorkee 247667, Uttarakhand, India
[2] Reg Res Inst Unani Med, Biochem & Pathol Lab, Patna 800008, Bihar, India
来源
RSC MEDICINAL CHEMISTRY | 2023年 / 14卷 / 11期
基金
英国惠康基金;
关键词
PENICILLIN-BINDING PROTEINS; HIGH-THROUGHPUT; LIPID-II; STREPTOCOCCUS-PNEUMONIAE; ANTIBIOTIC-RESISTANCE; TEICHOIC-ACID; TRANSPOSON MUTAGENESIS; ANTIBACTERIAL AGENTS; FLUOROMETRIC ASSAY; MUTANT LIBRARY;
D O I
10.1039/d3md00143a
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antimicrobial resistance (AMR) in bacterial pathogens is a worldwide health issue. The innovation gap in discovering new antibiotics has remained a significant hurdle in combating the AMR problem. Currently, antibiotics target various vital components of the bacterial cell envelope, nucleic acid and protein biosynthesis machinery and metabolic pathways essential for bacterial survival. The critical role of the bacterial cell envelope in cell morphogenesis and integrity makes it an attractive drug target. While a significant number of in-clinic antibiotics target peptidoglycan biosynthesis, several components of the bacterial cell envelope have been overlooked. This review focuses on various antibacterial targets in the bacterial cell wall and the strategies employed to find their novel inhibitors. This review will further elaborate on combining forward and reverse chemical genetic approaches to discover antibacterials that target the bacterial cell envelope. High-throughput chemical genetic screening strategies for bacterial cell envelope inhibitors.
引用
收藏
页码:2125 / 2154
页数:31
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