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Luminescence method for detection of aflatoxin B1 using ATP-releasing nucleotides

Determination of aflatoxin B1 (AFB1) is still a big issue in food safety. In this paper, we developed a luminescence AFB1 detection method combined with ATP-releasing nucleotides (ARNs) and AFB1 aptamer. Firstly, using a new coupling method, we synthesized two ARNs (dTP(4)A and dGP(4)A) in a yield o...

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Autores principales: Hu, Dongyue, Xiao, Shusen, Guo, Qiaqia, Yue, Rongrong, Geng, Demin, Ji, Debin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036674/
https://www.ncbi.nlm.nih.gov/pubmed/35479041
http://dx.doi.org/10.1039/d1ra03870b
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author Hu, Dongyue
Xiao, Shusen
Guo, Qiaqia
Yue, Rongrong
Geng, Demin
Ji, Debin
author_facet Hu, Dongyue
Xiao, Shusen
Guo, Qiaqia
Yue, Rongrong
Geng, Demin
Ji, Debin
author_sort Hu, Dongyue
collection PubMed
description Determination of aflatoxin B1 (AFB1) is still a big issue in food safety. In this paper, we developed a luminescence AFB1 detection method combined with ATP-releasing nucleotides (ARNs) and AFB1 aptamer. Firstly, using a new coupling method, we synthesized two ARNs (dTP(4)A and dGP(4)A) in a yield of 67% and 58%, respectively. The newly prepared ARNs show a much lower background. Then, we developed a new isothermal polymerase amplification method. In this method, two DNA hairpins were used to substitute the circle DNA template in rolling circle amplification. Using this amplification method and combined with AFB1 aptamer, a new AFB1 detection method is developed. A detection limit as low as 0.3 pM is achieved. This method is simple and efficient, and will have a great potential to be used for food safety and public health.
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spelling pubmed-90366742022-04-26 Luminescence method for detection of aflatoxin B1 using ATP-releasing nucleotides Hu, Dongyue Xiao, Shusen Guo, Qiaqia Yue, Rongrong Geng, Demin Ji, Debin RSC Adv Chemistry Determination of aflatoxin B1 (AFB1) is still a big issue in food safety. In this paper, we developed a luminescence AFB1 detection method combined with ATP-releasing nucleotides (ARNs) and AFB1 aptamer. Firstly, using a new coupling method, we synthesized two ARNs (dTP(4)A and dGP(4)A) in a yield of 67% and 58%, respectively. The newly prepared ARNs show a much lower background. Then, we developed a new isothermal polymerase amplification method. In this method, two DNA hairpins were used to substitute the circle DNA template in rolling circle amplification. Using this amplification method and combined with AFB1 aptamer, a new AFB1 detection method is developed. A detection limit as low as 0.3 pM is achieved. This method is simple and efficient, and will have a great potential to be used for food safety and public health. The Royal Society of Chemistry 2021-07-07 /pmc/articles/PMC9036674/ /pubmed/35479041 http://dx.doi.org/10.1039/d1ra03870b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Hu, Dongyue
Xiao, Shusen
Guo, Qiaqia
Yue, Rongrong
Geng, Demin
Ji, Debin
Luminescence method for detection of aflatoxin B1 using ATP-releasing nucleotides
title Luminescence method for detection of aflatoxin B1 using ATP-releasing nucleotides
title_full Luminescence method for detection of aflatoxin B1 using ATP-releasing nucleotides
title_fullStr Luminescence method for detection of aflatoxin B1 using ATP-releasing nucleotides
title_full_unstemmed Luminescence method for detection of aflatoxin B1 using ATP-releasing nucleotides
title_short Luminescence method for detection of aflatoxin B1 using ATP-releasing nucleotides
title_sort luminescence method for detection of aflatoxin b1 using atp-releasing nucleotides
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036674/
https://www.ncbi.nlm.nih.gov/pubmed/35479041
http://dx.doi.org/10.1039/d1ra03870b
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