School of Food Science and Biological Engineering, Hefei University of Technology, Hefei 230009, China.
School of Food Science and Biological Engineering, Hefei University of Technology-Xuancheng Campus, Xuancheng 242000, China.
Food Chem. 2022 Oct 15;391:133268. doi: 10.1016/j.foodchem.2022.133268. Epub 2022 May 20.
This work presented an electrochemical biosensor for the detection of virulence outer membrane protein A (ompA) gene of Cronobacter sakazakii (C. sakazakii), which was based on the mimic peroxidase activity of boron doped quantum dots-Au nanoparticles (BQDs-AuNPs) and a signal amplification strategy of exonuclease III (Exo III)-assisted target-recycling (EATR). The electrochemical signal was come from the electrochemical reduction of HO by BQDs-AuNPs nanozyme. Due to the enhanced peroxidase-mimic electrocatalytic efficiency of BQDs-AuNPs and the EATR strategy, the biosensor showed a broad linear range (1.0 × 10 - 1.0 × 10 mol L) and a low limit of detection (LOD, 4.0 × 10 mol L). The constructed biosensor could also be applied in direct detection of extracted DNA from C. sakazakii. A good linear relationship (7.8 - 7.8 × 10 CFU mL) between the logarithm concentration of C. sakazakii and electrochemical signal was obtained with a LOD of 2.6 CFU mL. The biosensor was applied in the detection of impA gene segments in contaminated infant formula with recoveries ranged in 83.4 - 108.2%.
本工作提出了一种用于检测阪崎克罗诺杆菌(Cronobacter sakazakii,C. sakazakii)毒力外膜蛋白 A(ompA)基因的电化学生物传感器,该传感器基于硼掺杂量子点-金纳米粒子(BQDs-AuNPs)的模拟过氧化物酶活性和外切酶 III(Exo III)辅助目标循环(EATR)的信号放大策略。电化学信号来自 BQDs-AuNPs 纳米酶对 HO 的电化学还原。由于 BQDs-AuNPs 的过氧化物酶模拟电催化效率增强和 EATR 策略,该生物传感器表现出较宽的线性范围(1.0×10 - 1.0×10 mol L)和较低的检测限(LOD,4.0×10 mol L)。该构建的生物传感器还可以直接检测从 C. sakazakii 提取的 DNA。C. sakazakii 的对数浓度与电化学信号之间存在良好的线性关系(7.8-7.8×10 CFU mL),检测限为 2.6 CFU mL。该生物传感器用于检测污染婴儿配方奶粉中的 impA 基因片段,回收率在 83.4-108.2%之间。