Synthesis and recycling of the mycobacterial cell envelope Katherine A Abrahams and Gurdyal S Besra

被引:31
作者
Abrahams, Katherine [1 ]
Besra, Gurdyal S. [1 ]
机构
[1] Univ Birmingham, Sch Biosci, Inst Microbiol & Infect, Birmingham B15 2TT, W Midlands, England
基金
英国医学研究理事会;
关键词
L; D-TRANSPEPTIDASE; 2; BETA-LACTAMASES; TUBERCULOSIS; ANTIBIOTICS; TRANSPORTER; EXPRESSION; RESISTANCE; MECHANISM; ARABINASE; AVIBACTAM;
D O I
10.1016/j.mib.2021.01.012
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mycobacterium tuberculosis (Mtb), the causative agent of the disease tuberculosis, is a recognised global health concern. The efficacy of the current treatment regime is under threat due to the emergence of antibiotic resistance, directing an urgent requirement for the discovery of new anti-tubercular agents and drug targets. The mycobacterial cell wall is a well-validated drug target for Mtb and is composed of three adaptive macromolecular structures, peptidoglycan, arabinogalactan and mycolic acids, an array of complex lipids and carbohydrates. The majority of the enzymes involved in cell wall synthesis have been established, whilst studies directed towards the mechanisms of remodelling and recycling have been neglected. This review briefly describes mycobacterial cell wall synthesis, and focuses on aspects of remodelling and recycling, thus highlighting opportunities for future research.
引用
收藏
页码:58 / 65
页数:8
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