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β-内酰胺酶诱导和革兰氏阴性菌的细胞壁代谢。

Beta-lactamase induction and cell wall metabolism in Gram-negative bacteria.

机构信息

Department of Animal Science, The University of Tennessee Knoxville, TN, USA.

出版信息

Front Microbiol. 2013 May 22;4:128. doi: 10.3389/fmicb.2013.00128. eCollection 2013.

Abstract

Production of beta-lactamases, the enzymes that degrade beta-lactam antibiotics, is the most widespread and threatening mechanism of antibiotic resistance. In the past, extensive research has focused on the structure, function, and ecology of beta-lactamases while limited efforts were placed on the regulatory mechanisms of beta-lactamases. Recently, increasing evidence demonstrate a direct link between beta-lactamase induction and cell wall metabolism in Gram-negative bacteria. Specifically, expression of beta-lactamase could be induced by the liberated murein fragments, such as muropeptides. This article summarizes current knowledge on cell wall metabolism, beta-lactam antibiotics, and beta-lactamases. In particular, we comprehensively reviewed recent studies on the beta-lactamase induction by muropeptides via two major molecular mechanisms (the AmpG-AmpR-AmpC pathway and BlrAB-like two-component regulatory system) in Gram-negative bacteria. The signaling pathways for beta-lactamase induction offer a broad array of promising targets for the discovery of new antibacterial drugs used for combination therapies. Therefore, to develop effective mitigation strategies against the widespread beta-lactam resistance, examination of the molecular basis of beta-lactamase induction by cell wall fragment is highly warranted.

摘要

β-内酰胺酶的产生是抗生素耐药性最广泛和最具威胁的机制,这些酶能够降解β-内酰胺类抗生素。过去,大量的研究集中在β-内酰胺酶的结构、功能和生态学上,而对其调控机制的研究则相对较少。最近,越来越多的证据表明,β-内酰胺酶的诱导与革兰氏阴性菌的细胞壁代谢之间存在直接联系。具体来说,β-内酰胺酶的表达可以被释放的肽聚糖片段(如肽聚糖)诱导。本文总结了细胞壁代谢、β-内酰胺类抗生素和β-内酰胺酶的最新研究进展。特别地,我们全面回顾了革兰氏阴性菌中肽聚糖通过两种主要分子机制(AmpG-AmpR-AmpC 途径和 BlrAB 样双组分调控系统)诱导β-内酰胺酶的最新研究。β-内酰胺酶诱导的信号通路为发现用于联合治疗的新型抗菌药物提供了广泛的有前途的靶标。因此,为了制定有效的缓解β-内酰胺广泛耐药性的策略,研究细胞壁片段诱导β-内酰胺酶的分子基础是非常必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc82/3660660/a6f0896ecef3/fmicb-04-00128-g001.jpg

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