Dual-electrode signal amplification self-powered biosensing platform based on nanozyme boosting target-induced DNA nanospace array for ultrasensitive detection of sugarcane Pokkah Boeng disease pathogenic bacteria

被引:0
|
作者
Song, Yujie [1 ]
Wang, Zeping [2 ]
Liao, Jie [2 ]
Zhang, Xiaoqiu [2 ]
Yan, Jun [2 ]
Luo, Hu [1 ]
Huang, Ke-Jing [1 ]
Tan, Xuecai [1 ]
Ya, Yu [2 ]
机构
[1] Guangxi Minzu Univ, Guangxi Collaborat Innovat Ctr Chem & Engn Forest, Sch Chem & Chem Engn, Educ Dept Guangxi Zhuang Autonomous Reg,Lab Opt el, Nanning 530006, Peoples R China
[2] Guangxi Acad Agr Sci, Nanning 530007, Peoples R China
关键词
Sugarcane pokkah boeng disease pathogenic; bacteria; Noble metal nanoparticles/metal oxide; nanozymes; Dual-electrode signal amplification; FUSARIUM;
D O I
10.1016/j.ijbiomac.2024.136423
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sugarcane is a crop with significant economic importance worldwide. However, pokkah boeng disease poses a serious threat to its production and the sustainable development. There is a pressing necessity for precise and portable detection methods. We develop a dual-electrode signal amplification biosensing platform, for highly sensitive detection of sugarcane pokkah boeng disease pathogenic bacteria. This innovative platform integrates highly catalytic AuNPs/Mn3O4 nanozymes with N-GDY, along with a target-induced development of DNA nanostructure arrays. AuNPs/N-GDY serves as dual electrode substrates, and AuNPs/Mn3O4 nanozymes are surface-loaded as the bioanode. The biocathode is constructed by introducing DNA nanospace arrays onto the electrode through target-induced methods. [Ru(NH3)6]3+ is embedded into the nucleic acid double-helix scaffold via electrostatic adsorption, generating an EOCV signal that is strongly correlated with the target concentration. To further enhance sensitivity, the detection platform is combined with a capacitor to amplify the detection signal, utilizing its high power density, which results in a 22.5-fold increase in sensitivity. The method offers a linear detection range of 0.0001 to 10,000 pM and an detection limit of 32.5 aM (S/N = 3). This method supplies a novel approach for real-time monitoring and competent oversight of pokkah boeng disease pathogenic bacteria.
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页数:11
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