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An unexpected similarity between antibiotic-resistant NDM-1 and beta-lactamase II from Erythrobacter litoralis

机译:耐抗生素的NDM-1与来自利多红杆菌的β-内酰胺酶II之间的意外相似性

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NDM-1 (New Delhi metallo-beta-lactamase) gene encodes a metallo-beta-lactamase (MBL) with high carbapenemase activity, which makes the host bacterial strain easily dispatch the last-resort antibiotics known as carbapenems and cause global concern. Here we present the bioinformatics data showing an unexpected similarity between NDM-1 and beta-lactamase II from Erythrobacter litoralis , a marine microbial isolate. We have further expressed these two mature proteins in E. coli cells, both of which present as a monomer with a molecular mass of 25 kDa. Antimicrobial susceptibility assay reveals that they share similar substrate specificities and are sensitive to aztreonam and tigecycline. The conformational change accompanied with the zinc binding visualized by nuclear magnetic resonance, Zn2+-bound NDM-1, adopts at least some stable tertiary structure in contrast to the metal-free protein. Our work implies a close evolutionary relationship between antibiotic resistance genes in environmental reservoir and in the clinic, challenging the antimicrobial resistance monitoring.
机译:NDM-1(新德里金属-β-内酰胺酶)基因编码具有高碳青霉烯酶活性的金属-β-内酰胺酶(MBL),这使得宿主细菌菌株很容易派发最后一种称为碳青霉烯酶的抗生素,并引起全球关注。在这里,我们介绍了生物信息学数据,该数据显示NDM-1与来自海洋微生物分离株利特罗红杆菌的β-内酰胺酶II之间出乎意料的相似性。我们已经在大肠杆菌细胞中进一步表达了这两种成熟蛋白,它们均以分子量为25 kDa的单体形式存在。抗菌药敏试验显示它们具有相似的底物特异性,并且对氨曲南和替加环素敏感。与核结合可见的结合锌的锌结合构象变化,Zn 2 + -结合的NDM-1,至少具有稳定的三级结构。无金属的蛋白质。我们的工作暗示环境储库和临床中的抗生素耐药基因之间存在密切的进化关系,这对监测耐药性提出了挑战。

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