大肠杆菌
多重耐药
纳米团簇
细菌
抗菌剂
微生物学
细胞内
抗菌活性
抗生素
化学
活性氧
细胞毒性
细菌细胞结构
生物
生物化学
体外
基因
有机化学
遗传学
作者
Hui-Qiong Jiang,Linyan Lu,Zhimin Weng,Kai-Yuan Huang,Yang Yu,Hao‐Hua Deng,Ying‐Ying Xu,Wei Chen,Quan‐Quan Zhuang
出处
期刊:ACS omega
[American Chemical Society]
日期:2023-11-28
卷期号:8 (49): 47123-47133
标识
DOI:10.1021/acsomega.3c07114
摘要
Multidrug-resistant bacterial infections, especially those caused by multidrug-resistant Escherichia coli (E. coli) bacteria, are an ever-growing threat because of the shrinking arsenal of efficacious antibiotics. Therefore, it is urgently needed to develop a kind of novel, long-term antibacterial agent effectively overcome resistant bacteria. Herein, we present a novel designed antibacterial agent-6-Aza-2-thiothymine-capped gold nanoclusters (ATT-AuNCs), which show excellent antibacterial activity against multidrug-resistant E. coli bacteria. The prepared AuNCs could permeabilize into the bacterial cell membrane via binding with a bivalent cation (e.g., Ca2+), followed by the generation of reactive oxygen species (e.g., •OH and •O2-), ultimately resulting in protein leakage from compromised cell membranes, inducing DNA damage and upregulating pro-oxidative genes intracellular. The AuNCs also speed up the wound healing process without noticeable hemolytic activity or cytotoxicity to erythrocytes and mammalian tissue. Altogether, the results indicate the great promise of ATT-AuNCs for treating multidrug-resistant E. coli bacterial infection.
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