柠檬酸循环
代谢途径
细胞内
细胞生物学
新陈代谢
三羧酸
程序性细胞死亡
生物
活性氧
细菌
微生物代谢
线粒体
氧化磷酸化
细胞代谢
生物化学
谷胱甘肽
细胞内寄生虫
细胞周期
抗氧化剂
细胞
细胞凋亡
代谢活性
抗菌剂
化学
细胞周期检查点
糖酵解
微生物学
碳纤维
信号转导
自噬
细胞呼吸
细菌细胞结构
代谢工程
作者
Shujing Deng,Chuanxin Chen,Qichao Tan,Danyang Wang,Heng Feng,Shiyu Liu,Jianfeng Xing,Ying Zhang
标识
DOI:10.1021/acsami.6c15149
摘要
Central carbon metabolism is essential for bacterial survival, making it a promising target for antimicrobial strategies. Bacterial cuproptosis-like and ferroptosis-like deaths are tightly linked to central carbon metabolism, yet their complete mechanistic cascades remain poorly understood. In addition, both death pathways are constrained by intracellular glutathione (GSH). Herein, we constructed chitosan-copper nanoclusters (CS-CuCs) as nanoantibiotics that selectively accumulate within bacteria to synergistically disrupt the tricarboxylic acid (TCA) cycle. CS-CuCs induces copper overload, impairs lipoylated and iron-sulfur (Fe-S) proteins, triggering cuproptosis-like death. Their peroxidase-like activity further generates reactive oxygen species, thereby exacerbating TCA cycle disruption. The subsequent dysfunction in central carbon metabolism reduces the supply of biosynthetic precursors of GSH, thereby compromising antioxidant defenses and provoking ferroptosis-like death. Metabolic collapse ultimately leads to cascading metabolic cell death in bacteria. Notably, CS-CuCs effectively eradicate biofilm-embedded and multidrug-resistant bacteria and exhibit excellent therapeutic efficacy in a mouse peritonitis-sepsis infection model. This study establishes a central carbon metabolism-targeted metabolic disruption strategy, providing a novel paradigm for triggering bacterial metabolic cell death.
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