Potential of Fluorophore Labeled Aptamers for Pseudomonas aeruginosa Detection in Drinking Water

被引:30
|
作者
Kim, Lan Hee [1 ]
Yu, Hye-Weon [2 ]
Kim, Yang-Hoon [3 ]
Kim, In S. [1 ]
Jang, Am [4 ]
机构
[1] GIST, Sch Environm Sci & Engn, Kwangju 500712, South Korea
[2] Univ Arizona, Dept Soil Water & Environm Sci, Coll Agr & Life Sci, Tucson, AZ USA
[3] Chungbuk Natl Univ, Dept Microbiol, Cheongju 361763, South Korea
[4] Sungkyunkwan Univ, Dept Civil & Environm Engn, Suwon 440746, South Korea
来源
JOURNAL OF THE KOREAN SOCIETY FOR APPLIED BIOLOGICAL CHEMISTRY | 2013年 / 56卷 / 02期
基金
新加坡国家研究基金会;
关键词
aptamer; biosensor; fluorescein isothiocyannate; Pseudomonas aeruginosa; quantum dot; DNA APTAMERS; BIOSENSORS; BACTERIA; CAPTURE; BINDING; PROBES; SIZE;
D O I
10.1007/s13765-013-3019-7
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Pseudomonas aeruginosa has been considered as a representative pathogenic bacteria in drinking water. In order to detect P aeruginosa, aptamers were utilized in this study. In particular, fluorescein isothiocyannate (FITC) and quantum dot (QD) were used for aptamer labeling. FITC-labeled aptamers showed higher binding capacity with optimal incubation time of 30 min compared to QD-labeled aptamers. However, incubation speed did not have any effect on the binding capacity of FITC-labeled aptamers to bacteria. Aptamer-binding capacity was measured according to varying cell concentrations of 0, 10, 100, and 1000 cells/mL. As a result, the limit of detection, limit of quantification, and limit of linearity of P aeruginosa were 5.07, 5.64, and 100 cells/mL, respectively. The low detection limit shows the fluorophore-labeled aptamer potential to detect P aeruginosa labeling in the field.
引用
收藏
页码:165 / 171
页数:7
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