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Differential gene regulation in the Ag nanoparticle and Ag+-induced silver stress response inEscherichia coli: A full transcriptomic profile

硝酸银 大肠杆菌 银纳米粒子 基因表达 基因表达调控 生物 化学 转录组 基因 细胞生物学 生物物理学 生物化学 分子生物学 纳米颗粒 材料科学 核化学 纳米技术
作者
Jonathan S. McQuillan,Andrew M. Shaw
出处
期刊:Nanotoxicology [Taylor & Francis]
卷期号:8 (sup1): 177-184 被引量:109
标识
DOI:10.3109/17435390.2013.870243
摘要

We report the whole-transcriptome response of Escherichia coli bacteria to acute treatment with silver nanoparticles (AgNPs) or silver ions [Ag(I)] as silver nitrate using gene expression microarrays. In total, 188 genes were regulated by both silver treatments, 161 were up-regulated and 27 were down-regulated. Significant regulation was observed for heat shock response genes in line with protein denaturation associated with protein structure vulnerability indicating Ag(I)-labile –SH bonds. Disruption to iron–sulphur clusters led to the positive regulation of iron–sulphur assembly systems and the expression of genes for iron and sulphate homeostasis. Further, Ag ions induced a redox stress response associated with large (>600-fold) up-regulation of the E. coli soxS transcriptional regulator gene. Ag(I) is isoelectronic with Cu(I), and genes associated with copper homeostasis were positively regulated indicating Ag(I)-activation of copper signalling. Differential gene expression was observed for the silver nitrate and AgNP silver delivery. Nanoparticle delivery of Ag(I) induced the differential regulation of 379 genes; 309 genes were uniquely regulated by silver nanoparticles and 70 genes were uniquely regulated by silver nitrate. The differential silver nanoparticle–silver nitrate response indicates that the toxic effect of labile Ag(I) in the system depends upon the mechanism of delivery to the target cell.
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