Development of highly sensitive electrochemical genosensor based on multiwalled carbon nanotubes-chitosan-bismuth and lead sulfide nanoparticles for the detection of pathogenic Aeromonas

被引:48
作者
Fernandes, Antonio Maximiano [1 ]
Abdalhai, Mandour H. [1 ]
Ji, Jian [1 ]
Xi, Bing-Wen [2 ]
Xie, Jun [2 ]
Sun, Jiadi [1 ]
Noeline, Rasoamandrary [1 ]
Lee, Byong H. [3 ]
Sun, Xiulan [1 ]
机构
[1] Jiangnan Univ, Synerget Innovat Ctr Food Safety & Nutr, Sch Food Sci & Technol, State Key Lab Food Sci & Technol, Wuxi 7214122, Jiangsu, Peoples R China
[2] Chinese Acad Fishery Sci, Minist Agr, Freshwater Fisheries Res Ctr, Key Lab Freshwater Fisheries & Germplasm Resource, Wuxi 214081, Peoples R China
[3] Jiangnan Univ, Sch Biotechnol, Wuxi 214122, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemical biosensor; Aeromonas; Lead sulfide nanoparticles; Foodborne pathogen; ANODIC-STRIPPING VOLTAMMETRY; SOLID-PHASE EXTRACTION; DNA HYBRIDIZATION; FILM ELECTRODE; BIOSENSOR; SENSOR; WATER; SAMPLES; RECOGNITION; HYDROPHILA;
D O I
10.1016/j.bios.2014.07.054
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
In this paper, we reported the construction of new high sensitive electrochemical genosensor based on multiwalled carbon nanotubes-chitosan-bismuth complex (MWCNT-Chi-Bi) and lead sulfide nanopartides for the detection of pathogenic Aeromonas. Lead sulfide nanoparticles capped with 5'-(NH2) oligonucleotides thought amide bond was used as signalizing probe DNA (sz-DNA) and thiol-modified oligonucleotides sequence was used as fixing probe DNA (fDNA). The two probes hybridize with target Aeromonas DNA (tDNA) sequence (fDNA-tDNA-szDNA). The signal of hybridization is detected by differential pulse voltammetry (DPV) after electrodeposition of released lead nanoparticles (PbS) from sz-DNA on the surface of glass carbon electrode decorated with MWCNT-Chi-Bi, which improves the deposition and traducing electrical signal. The optimization of incubation time, hybridization temperature, deposition potential, deposition time and the specificity of the probes were investigated. Our results showed the highest sensibility to detect the target gene when compared with related biosensors and polymerase chain reaction (PCR). The detection limit for this biosensor was 1.0 x 10(-14) M. We could detect lower than 10(2) CFU mL(-1) of Aeromonas in spiked tap water. This method is rapid and sensitive for the detection of pathogenic bacteria and would become a potential application in biomedical diagnosis, food safety and environmental monitoring. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:399 / 406
页数:8
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