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DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
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Pablo Llano-Suárez1, Adrián Sánchez-Visedo1, Inmaculada Ortiz-Gómez1

  • 1Department of Physical and Analytical Chemistry, University of Oviedo, c/Julián Clavería, 8, 33006 Oviedo, Spain.

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A new DNA-based method using gold nanoparticles (AuNPs) offers sensitive and rapid detection of sesame DNA in food. This colorimetric approach enhances food safety by enabling simple, affordable allergen analysis.

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AuNPsMNAzymesanalytical signal amplificationcolor analysisfood safetysesame allergen

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Area of Science:

  • Food Science
  • Analytical Chemistry
  • Nanotechnology

Background:

  • Food safety is paramount in the food and agriculture sectors.
  • Rapid and sensitive detection of allergens, supplements, and pollutants is crucial.
  • Miniaturized analytical methods are needed for on-site food analysis.

Purpose of the Study:

  • To develop a novel bioanalytical method for detecting sesame DNA in food samples.
  • To enhance sensitivity and accuracy using DNA-functionalized gold nanoparticles (AuNPs) and multicomponent nucleic acid enzymes (MNAzymes).
  • To provide a simple, affordable, and decentralized detection method for food allergens.

Main Methods:

  • Utilized DNA-functionalized gold nanoparticles (AuNPs) for colorimetric detection of sesame DNA.
  • Employed multicomponent nucleic acid enzymes (MNAzymes) for isothermal signal amplification.
  • Incorporated open-source software for unbiased color analysis to improve accuracy and sensitivity.

Main Results:

  • Successfully detected sesame DNA in various food matrices, including sesame seed, sesame oil, olive oil, and sunflower oil.
  • Demonstrated a color change (blue to red) proportional to sesame DNA concentration.
  • Achieved high sensitivity and accuracy through MNAzyme amplification and software-assisted color analysis.

Conclusions:

  • The developed method offers a simple, affordable, and highly sensitive approach for DNA detection in food.
  • This bioanalytical methodology bypasses the need for complex instrumentation or procedures.
  • It presents a viable alternative for decentralized food allergen testing and safety control.