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Amplification-free and label-free rapid detection of Staphylococcus aureus using solution-gated graphene transistor-based DNA biosensor with hybridization enhancement by interface engineering

生物传感器 DNA 石墨烯 接口(物质) 金黄色葡萄球菌 晶体管 纳米技术 材料科学 DNA–DNA杂交 光电子学 化学 生物 工程类 遗传学 生物化学 细菌 电气工程 肺表面活性物质 吉布斯等温线 电压
作者
Jiayuan Zheng,Jinhua Li,T.D. Lin,Zhanpeng Ren,Fucheng Wang,Zhonghao Shi,Haiyang Yu,Wei Jiang,Wei Tang
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:495: 153329-153329 被引量:4
标识
DOI:10.1016/j.cej.2024.153329
摘要

Staphylococcus aureus (S. aureus) is one of the leading causes of foodborne illnesses worldwide, posing a significant risk to food quality and safety. However, conventional detection methods often require complex amplification and labeling procedures, which are time consuming and expensive. In this study, an extremely sensitive electrochemical biosensor using a solution-gated graphene transistor (SGGT) was constructed for the amplification-free and label-free rapid detection of S. aureus by utilizing specific single-stranded DNA (ssDNA) to modify the gold (Au) sensing gate. This modified ssDNA was designed to hybridize with the target S. aureus DNA sequence. Interface engineering of the ssDNA-modified sensing gate via optimization of specific target and probe sequences was proposed to improve its hybridization efficiency. This enabled the sensitive quantitative detection of S. aureus DNA. The resulting biosensor exhibited excellent specificity in distinguishing non-complementary, 3-base/9-base DNA mismatch targets of S. aureus DNA and the specific DNA sequences of other common pathogenic bacteria. It also enabled the rapid detection of extracted target DNA sequences in solution (within 27 min) and had a low limit of detection (LoD) of 10−17 M over a wide linear detection range (10−17–10−8 M). Furthermore, the newly-developed biosensor facilitated the real-time and on-site detection of the S. aureus genome (ATCC 6538) with LoD of 10−17 M (103 CFU/mL) in a portable smart-sensing system. This suggests a promising future for the development of rapid, label-free, and amplification-free detection of foodborne illnesses using low-cost, highly sensitive SGGT DNA biosensors with appropriate functionalization and interface engineering of the sensing electrode.
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