New function of molybdenum trioxide nanoplates: Toxicity towards pathogenic bacteria through membrane stress

被引:77
作者
Krishnamoorthy, Karthikeyan [1 ]
Veerapandian, Murugan [2 ,3 ]
Yun, Kyusik [2 ]
Kim, Sang Jae [1 ,4 ]
机构
[1] Jeju Natl Univ, Dept Mech Engn, Nanomat & Syst Lab, Jeju 690456, South Korea
[2] Gachon Univ, Dept Bionanotechnol, Gyeonggi Do 461701, South Korea
[3] Univ Montreal, Dept Chim, Montreal, PQ H3C 3J7, Canada
[4] Jeju Natl Univ, Dept Mechatron Engn, Jeju 690456, South Korea
基金
新加坡国家研究基金会;
关键词
MoO3; Nanoplates; Antibacterial activity; Membrane disruption; Minimum inhibitory concentration; ANTIBACTERIAL; NANOPARTICLES; MECHANISM; GRAPHENE; GROWTH; CANCER;
D O I
10.1016/j.colsurfb.2013.08.026
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Inorganic nanostructures are highly recognized for their potential use in the development of new functional materials for biomedical applications. In this study, we investigated the antibacterial efficiency of molybdenum trioxide (MoO3) nanoplates against four types of pathogenic bacteria. MoO3 nanoplates are synthesized by a simple wet chemical approach. X-ray diffraction and FT-IR analysis showed the presence of an orthorhombic phase of MoO3 nanoplates. Field emission scanning electron microscope studies confirmed the formation of plate-like structures of MoO3. The minimum inhibitory concentration (MIC) of MoO3 nanoplates against pathogenic bacteria was evaluated using a microdilution method. MICs such as 8 mu g/mL (against Escherichia coli and Salmonella typhimurium), 16 mu g/mL (against Enterococcus faecalis), and 8 mu g/mL (against Bacillus subtilis) show that MoO3 nanoplates have predominant antibacterial activity compared to the standard antibiotic, kanamycin. Evaluation of bacterial enzymatic (beta-D-galactosidase) activity in the hydrolysis of o-nitrophenol and beta-D-galactopyranoside suggested the disruption of the bacterial cell wall mechanism responsible for bacterial toxicity. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:521 / 524
页数:4
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