Exposure to High Dosage of Gold Nanoparticles Accelerates Growth Rate by Modulating Ribosomal Protein Expression

胶体金 枯草芽孢杆菌 酿酒酵母 核糖体蛋白 细胞生长 大肠杆菌 核糖体 金融时报 生物物理学 蛋白质生物合成 细菌 细菌生长 细胞生物学 细胞分裂 生物 细胞 细菌细胞结构 化学 酵母 生物化学 纳米颗粒 纳米技术 核糖核酸 材料科学 基因 遗传学
作者
Shabina Quadir,Nuha Abeer Khan,Deepak Kumar Singh,Amir Faraz,Gagan Deep Jhingan,Mohan C. Joshi
出处
期刊:ACS Nano [American Chemical Society]
卷期号:17 (16): 15529-15541 被引量:2
标识
DOI:10.1021/acsnano.3c01973
摘要

Gold nanoparticles (AuNPs) have been utilized in various biomedical applications including diagnostics and drug delivery. However, the cellular and metabolic responses of cells to these particles remain poorly characterized. In this study, we used bacteria (Escherichia coli and Bacillus subtilis) and a fungus (Saccharomyces cerevisiae) as model organisms to investigate the cellular and metabolic effects of exposure to different concentrations of citrate-capped spherical AuNPs with diameters of 5 and 10 nm. In different growth media, the synthesized AuNPs displayed stability and microorganisms exhibited uniform levels of uptake. Exposure to a high concentration of AuNPs (1012 particles) resulted in a reduced cell division time and a 2-fold increase in cell density in both bacteria and fungus. The exposed cells exhibited a decrease in average cell size and an increase in the expression of FtsZ protein (cell division marker), further supporting an accelerated growth rate. Notably, exposure to such a high concentration of AuNPs did not induce DNA damage, envelope stress, or a general stress response in bacteria. Differential whole proteome analysis revealed modulation of ribosomal protein expression upon exposure to AuNPs in both E. coli and S. cerevisiae. Interestingly, the accelerated growth observed upon exposure to AuNPs was sensitive to sub-minimum inhibitory concentration (sub-MIC) concentration of drugs that specifically target ribosome assembly and recycling. Based upon these findings, we hypothesize that exposure to high concentrations of AuNPs induces stress on the translation machinery. This leads to an increase in the protein synthesis rate by modulating ribosome assembly, which results in the rapid proliferation of cells.

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