Development of a real-time LAMP assay for monofloral honey authentication using rape honey

The objective of this study was to establish a real-time LAMP assay for authentication of rape (Brassica napus) honey to protect consumers from commercial honey adulteration. The LAMP primers targeting the internal transcribed spacer (ITS) of Brassica napus were designed, and its specificity was tes...

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Main Authors: Yongzhen Wang, Meng Zhang, Deguo Wang, Yongqing Zhang, Xuexue Jiao, Yanhong Liu
Format: Article
Language:English
Published: Taylor & Francis Group 2020-01-01
Series:CyTA - Journal of Food
Subjects:
Online Access:http://dx.doi.org/10.1080/19476337.2020.1749135
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spelling doaj-dbbe12f3b2d246569e07a69e6149710d2020-12-17T14:55:55ZengTaylor & Francis GroupCyTA - Journal of Food1947-63371947-63452020-01-0118130931410.1080/19476337.2020.17491351749135Development of a real-time LAMP assay for monofloral honey authentication using rape honeyYongzhen Wang0Meng Zhang1Deguo Wang2Yongqing Zhang3Xuexue Jiao4Yanhong Liu5Xuchang UniversityHenan University of Science and TechnologyXuchang UniversityXuchang UniversityXuchang UniversityAgricultural Research Service, United States Department of AgricultureThe objective of this study was to establish a real-time LAMP assay for authentication of rape (Brassica napus) honey to protect consumers from commercial honey adulteration. The LAMP primers targeting the internal transcribed spacer (ITS) of Brassica napus were designed, and its specificity was tested. The LAMP reaction temperature was also optimized, and the detection limit of the LAMP assay was determined with a serial dilution of genomic DNA from the seeds of Brassica napus. The results showed that the real-time LAMP assay can accurately and specifically detect the rape component in honey, and the detection limit was 10 pg genomic DNA of Brassica napus. Data on monofloral honey samples indicate that the real-time LAMP assay was 100% in concordance with the reported TaqManTM PCR assay. This study provides a promising solution for facilitating the authentication of rape honey in food retail market.http://dx.doi.org/10.1080/19476337.2020.1749135loop-mediated isothermal amplification (lamp)rape honeyinternal transcribed spacer (its)
collection DOAJ
language English
format Article
sources DOAJ
author Yongzhen Wang
Meng Zhang
Deguo Wang
Yongqing Zhang
Xuexue Jiao
Yanhong Liu
spellingShingle Yongzhen Wang
Meng Zhang
Deguo Wang
Yongqing Zhang
Xuexue Jiao
Yanhong Liu
Development of a real-time LAMP assay for monofloral honey authentication using rape honey
CyTA - Journal of Food
loop-mediated isothermal amplification (lamp)
rape honey
internal transcribed spacer (its)
author_facet Yongzhen Wang
Meng Zhang
Deguo Wang
Yongqing Zhang
Xuexue Jiao
Yanhong Liu
author_sort Yongzhen Wang
title Development of a real-time LAMP assay for monofloral honey authentication using rape honey
title_short Development of a real-time LAMP assay for monofloral honey authentication using rape honey
title_full Development of a real-time LAMP assay for monofloral honey authentication using rape honey
title_fullStr Development of a real-time LAMP assay for monofloral honey authentication using rape honey
title_full_unstemmed Development of a real-time LAMP assay for monofloral honey authentication using rape honey
title_sort development of a real-time lamp assay for monofloral honey authentication using rape honey
publisher Taylor & Francis Group
series CyTA - Journal of Food
issn 1947-6337
1947-6345
publishDate 2020-01-01
description The objective of this study was to establish a real-time LAMP assay for authentication of rape (Brassica napus) honey to protect consumers from commercial honey adulteration. The LAMP primers targeting the internal transcribed spacer (ITS) of Brassica napus were designed, and its specificity was tested. The LAMP reaction temperature was also optimized, and the detection limit of the LAMP assay was determined with a serial dilution of genomic DNA from the seeds of Brassica napus. The results showed that the real-time LAMP assay can accurately and specifically detect the rape component in honey, and the detection limit was 10 pg genomic DNA of Brassica napus. Data on monofloral honey samples indicate that the real-time LAMP assay was 100% in concordance with the reported TaqManTM PCR assay. This study provides a promising solution for facilitating the authentication of rape honey in food retail market.
topic loop-mediated isothermal amplification (lamp)
rape honey
internal transcribed spacer (its)
url http://dx.doi.org/10.1080/19476337.2020.1749135
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