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Sci Rep. 2016 Oct 12;6:35243. doi: 10.1038/srep35243.

Toxicity of ZnO and TiO2 to Escherichia coli cells.

Author information

1
Dept. of Physics, Univ. of Hong Kong, Pokfulam Road, Hong Kong.
2
School of Energy and Environment, City University of Hong Kong, Kowloon Tong, Hong Kong.
3
School of Biological Sciences, Univ. of Hong Kong, Pokfulam Road, Hong Kong.
4
Dept. of Physics, South University of Science and Technology of China, Shenzhen, China.
5
Pharmaceutical and Life Sciences Division, Waters Corporation, Manchester, UK.
6
Dept. of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.
7
Dept. of Chemistry, Univ. of Hong Kong, Pokfulam Road, Hong Kong.

Abstract

We performed a comprehensive investigation of the toxicity of ZnO and TiO2 nanoparticles using Escherichia coli as a model organism. Both materials are wide band gap n-type semiconductors and they can interact with lipopolysaccharide molecules present in the outer membrane of E. coli, as well as produce reactive oxygen species (ROS) under UV illumination. Despite the similarities in their properties, the response of the bacteria to the two nanomaterials was fundamentally different. When the ROS generation is observed, the toxicity of nanomaterial is commonly attributed to oxidative stress and cell membrane damage caused by lipid peroxidation. However, we found that significant toxicity does not necessarily correlate with up-regulation of ROS-related proteins. TiO2 exhibited significant antibacterial activity, but the protein expression profile of bacteria exposed to TiO2 was different compared to H2O2 and the ROS-related proteins were not strongly expressed. On the other hand, ZnO exhibited lower antibacterial activity compared to TiO2, and the bacterial response involved up-regulating ROS-related proteins similar to the bacterial response to the exposure to H2O2. Reasons for the observed differences in toxicity and bacterial response to the two metal oxides are discussed.

PMID:
27731373
PMCID:
PMC5378928
DOI:
10.1038/srep35243
[Indexed for MEDLINE]
Free PMC Article

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