4.7 Article

PCR-assisted impedimetric biosensor for colibactin-encoding pks genomic island detection in E. coli samples

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 413, 期 18, 页码 4673-4680

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03404-6

关键词

Electrochemical impedance spectroscopy; DNA biosensor; Polyketide synthase genomic island; Polymerase chain reaction (PCR)

资金

  1. NSF-CREST [1736093]
  2. NIH-RISE Fellowship [5R25GM061151]
  3. Puerto Rico NASA Space Grant Consortium [NNX10AM80H]
  4. Australian Academy of Science
  5. Division Of Human Resource Development
  6. Direct For Education and Human Resources [1736093] Funding Source: National Science Foundation

向作者/读者索取更多资源

A fast PCR-assisted impedimetric biosensor was developed for selective detection of the clbN gene in real Escherichia coli samples, responsible for producing the harmful genotoxin colibactin. The study demonstrated successful identification of target DNA by monitoring changes in charge transfer resistance values before and after PCR. The biosensor showed effective distinction between target interaction, with a calculated limit of detection of 17 ng/μL.
A fast PCR-assisted impedimetric biosensor was developed for the selective detection of the clbN gene from the polyketide synthase (pks) genomic island in real Escherichia coli samples. This genomic island is responsible for the production of colibactin, a harmful genotoxin that has been associated with colorectal cancer. The experimental protocol consisted of immobilizing the designated forward primer onto an Au electrode surface to create the sensing probe, followed by PCR temperature cycling in blank, positive, and negative DNA controls. Target DNA identification was possible by monitoring changes in the system's charge transfer resistance values (R-ct) before and after PCR treatment through electrochemical impedance spectroscopy (EIS) analysis. Custom-made, flexible gold electrodes were fabricated using chemical etching optical lithography. A PCR cycle study determined the optimum conditions to be at 6 cycles providing fast results while maintaining a good sensitivity. EIS data for the DNA recognition process demonstrated the successful distinction between target interaction resulting in an increase in resistance to charge transfer (R-ct) percentage change of 176% for the positive DNA control vs. 21% and 20% for the negative and non-DNA-containing controls, respectively. Results showed effective fabrication of a fast, PCR-based electrochemical biosensor for the detection of pks genomic island with a calculated limit of detection of 17 ng/mu L.

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