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利奈唑胺类似物L3耐药突变的特征分析 。 (你提供的原文似乎不完整,翻译可能不太精准,你可以补充完整原文以便我给出更准确的译文。)

Characterization of Linezolid-Analogue L3-Resistance Mutation in .

作者信息

Zanfardino Anna, Di Napoli Michela, Migliore Federica, Hay Mele Bruno, Soriente Annunziata, De Rosa Margherita, Notomista Eugenio, Varcamonti Mario

机构信息

Department of Biology, University of Naples Federico II, Via Cintia, 80126 Naples, Italy.

Department of Chemistry and Biology "Zambelli", University of Salerno, Via Giovanni Paolo II, 132, 84084 Fisciano, Italy.

出版信息

Microorganisms. 2023 Mar 8;11(3):700. doi: 10.3390/microorganisms11030700.

Abstract

In a previous study, a linezolid analogue, called 10f, was synthesized. The 10f molecule has an antimicrobial activity comparable to that of the parental compound. In this study, we isolated a () strain resistant to 10f. After sequencing the 23S rRNA and the ribosomal proteins L3 (rplC) and L4 (rplD) genes, we found that the resistant phenotype was associated with a single mutation G359U in rplC bearing to the missense mutation G120V in the L3 protein. The identified mutation is far from the peptidyl transferase center, the oxazolidinone antibiotics binding site, thus suggesting that we identified a new and interesting example of a long-range effect in the ribosome structure.

摘要

在之前的一项研究中,合成了一种名为10f的利奈唑胺类似物。10f分子具有与母体化合物相当的抗菌活性。在本研究中,我们分离出一株对10f耐药的()菌株。对23S rRNA以及核糖体蛋白L3(rplC)和L4(rplD)基因进行测序后,我们发现耐药表型与rplC中一个单一突变G359U相关,该突变导致L3蛋白中出现错义突变G120V。所鉴定的突变远离肽基转移酶中心,即恶唑烷酮类抗生素结合位点,因此表明我们发现了核糖体结构中远距离效应的一个新的有趣例子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/119f/10054786/644f1e56f1a0/microorganisms-11-00700-g001.jpg

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