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缺乏DNA甲基转移酶菌株的抗生素毒性概况

Antibiotic Toxicity Profiles of Strains Lacking DNA Methyltransferases.

作者信息

Chen Zheng, Wang Hailin

机构信息

State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

ACS Omega. 2021 Mar 15;6(11):7834-7840. doi: 10.1021/acsomega.1c00378. eCollection 2021 Mar 23.

Abstract

Antibiotic-resistant bacteria are causing more antibiotic treatment failures. Developing new antibiotics and identifying bacterial targets will help to mitigate the emergence and reduce the spread of antibiotic resistance in the environment. We investigated whether DNA methyltransferase (MTase) can be an adjunct target for improving antibiotic toxicity. We used as an example. The genes encoding DNA adenine MTase and cytosine MTase, and , respectively, were separately knocked out using the λRed system in MG1655. MG1655 and the two knockout strains were separately exposed in 96-well plates to 20 antibiotics from five classes. The EC values of almost all of the tested antibiotics were lower in the and knockout lines than that of the control. Our statistical analysis showed that the variations observed in EC values were independent of the mechanism underlying each antibiotic's mechanistic action.

摘要

抗生素耐药菌导致越来越多的抗生素治疗失败。开发新的抗生素并确定细菌靶点将有助于减轻抗生素耐药性在环境中的出现并减少其传播。我们研究了DNA甲基转移酶(MTase)是否可以作为增强抗生素毒性的辅助靶点。我们以[具体细菌名称]为例。分别使用λRed系统在大肠杆菌MG1655中敲除编码DNA腺嘌呤MTase和胞嘧啶MTase的基因,即[基因名称1]和[基因名称2]。将MG1655和这两种敲除菌株分别在96孔板中暴露于五类中的20种抗生素。几乎所有测试抗生素在[基因名称1]和[基因名称2]敲除株中的半数有效浓度(EC值)均低于对照。我们的统计分析表明,观察到的EC值变化与每种抗生素作用机制背后的机制无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc3d/7992158/cc4000b19f8f/ao1c00378_0002.jpg

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