分枝杆菌长体单元的认识及其与其他模式生物的比较分析

Preeti Jain
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引用次数: 0

摘要

据报告,2021年全球结核病发病率为1060万例,死亡人数为160万人,这表明这种由结核分枝杆菌病原体引起的疾病难以治疗,需要探索新的可能的治疗干预措施。为了确定新的药物靶点,详细了解每种病原体的基本生理过程非常重要。细胞分裂是维持细菌繁殖状态的基本生理过程。这一过程需要细胞壁的重塑,这是由两个时空组织的复合体,长体和分裂体来完成的。细长体和分裂体这两种复合物分别在细胞的两极或隔膜上合成肽聚糖(PG)。本文就分枝杆菌长体复合体的不同特征和组成作一综述。这种理解将有助于确定新的药物靶点和设计分枝杆菌特异性药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Understanding Elongasome Unit of Mycobacterium and its Comparative Analysis with Other Model Organisms
The reported incidences of 10.6 million tuberculosis cases worldwide with 1.6 million deaths in 2021 indicate that this disease, caused by Mycobacterium tuberculosis pathogen is difficult to treat and requires exploring newer possible therapeutic interventions. To identify novel drug targets, it is important to understand the basic physiological processes of each pathogen in detail. Cell division is the fundamental physiological process which maintains the replicative state of bacteria. This process requires remodelling of the cell wall, which is performed by two spatio-temporal organized complexes, elongasome and divisome. These two complexes, elongasome and divisome function in synthesis of peptidoglycan (PG) at poles or septum of the cell, respectively. This review article is focused on illustrating differential features and composition of mycobacterial elongasome complex. This sort of understanding would allow identification of new drug targets and design of Mycobacterium specific drugs.
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