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RodA 作为枯草芽孢杆菌中缺失的糖基转移酶及其在肽聚糖聚合酶途径中的抗生素发现。

RodA as the missing glycosyltransferase in Bacillus subtilis and antibiotic discovery for the peptidoglycan polymerase pathway.

机构信息

The Centre for Bacterial Cell Biology, Baddiley-Clark Building, Medical School, Newcastle University, Richardson Road, Newcastle upon Tyne NE2 4AX, UK.

Demuris Ltd, Newcastle Biomedicine Bio-Incubators, Framlington Place, Newcastle upon Tyne NE2 4HH, UK.

出版信息

Nat Microbiol. 2017 Jan 13;2:16253. doi: 10.1038/nmicrobiol.2016.253.

Abstract

The bacterial cell wall is a highly conserved essential component of most bacterial groups. It is the target for our most frequently used antibiotics and provides important small molecules that trigger powerful innate immune responses. The wall is composed of glycan strands crosslinked by short peptides. For many years, the penicillin-binding proteins were thought to be the key enzymes required for wall synthesis. RodA and possibly other proteins in the wider SEDS (shape, elongation, division and sporulation) family have now emerged as a previously unknown class of essential glycosyltranferase enzymes, which play key morphogenetic roles in bacterial cell wall synthesis. We provide evidence in support of this role and the discovery of small natural product molecules that probably target these enzymes. The SEDS proteins have exceptional potential as targets for new antibacterial therapeutic agents.

摘要

细菌细胞壁是大多数细菌群体高度保守的必需成分。它是我们最常使用的抗生素的靶标,并且提供了引发强大先天免疫反应的重要小分子。细胞壁由糖链通过短肽交联而成。多年来,青霉素结合蛋白被认为是细胞壁合成所需的关键酶。现在,RodA 和更广泛的 SEDS(形状、伸长、分裂和孢子形成)家族中的其他一些蛋白质已经成为一个以前未知的必需糖基转移酶酶类,它们在细菌细胞壁合成中发挥关键的形态发生作用。我们提供了支持这一作用的证据,以及发现可能靶向这些酶的小分子天然产物分子。SEDS 蛋白作为新型抗菌治疗药物的靶标具有巨大的潜力。

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