Ding Zhenhao, Kasahara Hiromichi, Nakano Michihiko, Suehiro Junya
Department of Electrical and Electronic Engineering, Graduate School of Information Science and Electrical Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
IET Nanobiotechnol. 2017 Aug;11(5):562-567. doi: 10.1049/iet-nbt.2016.0186.
In this study, an electrical DNA detection method was applied to bacterial detection. DNA was extracted from bacteria and amplified by polymerase chain reaction. The microbeads were labelled with amplicons, altering their surface conductance and therefore their dielectrophoresis characteristics. Amplicon-labelled microbeads could thus be trapped within a high-strength electric field, where they formed a pearl chain between the electrodes, resulting in an increased conductance between the electrodes. This method reduces the amplicon detection time from 1-2 h to 15 min, compared with the conventional method. The presented method realised quantitative detection of specific bacteria at concentrations above 1 × 10 and 2.4 × 10 CFU/ml for bacterial solutions with and without other bacterial presence, respectively.
在本研究中,一种电DNA检测方法被应用于细菌检测。从细菌中提取DNA并通过聚合酶链反应进行扩增。微珠用扩增子标记,改变其表面电导率,从而改变其介电泳特性。因此,扩增子标记的微珠可以被困在高强度电场中,在电极之间形成珍珠链,导致电极之间的电导率增加。与传统方法相比,该方法将扩增子检测时间从1 - 2小时缩短至15分钟。所提出的方法分别实现了对浓度高于1×10和2.4×10 CFU/ml的特定细菌的定量检测,适用于有和没有其他细菌存在的细菌溶液。