Primer pairs specificity test for frog meat identification using PCR technique

Halal food assurance is becoming more important with the growth of the halal industry globally. Adulteration of halal meat products using non-halal sources such as pork, dog, boar, and even frog meat has become a major problem for moslems. The purpose of this study is to initiate the method for frog...

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Main Authors: Haryono, Norman Yoshi, Khusufi, Rizqi Layli, Pangesti, Delia Wahyu, Susanti, Evi, Mariana, Rina Rifqie, Wardani, Hartati Eko, Salim, Norazlinaliza
Format: Article
Published: Universitas Gadjah Mada, Indonesia 2023
Online Access:http://psasir.upm.edu.my/id/eprint/110064/
https://jurnal.ugm.ac.id/ijc/article/view/83626
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Institution: Universiti Putra Malaysia
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spelling my.upm.eprints.1100642024-09-05T07:26:36Z http://psasir.upm.edu.my/id/eprint/110064/ Primer pairs specificity test for frog meat identification using PCR technique Haryono, Norman Yoshi Khusufi, Rizqi Layli Pangesti, Delia Wahyu Susanti, Evi Mariana, Rina Rifqie Wardani, Hartati Eko Salim, Norazlinaliza Halal food assurance is becoming more important with the growth of the halal industry globally. Adulteration of halal meat products using non-halal sources such as pork, dog, boar, and even frog meat has become a major problem for moslems. The purpose of this study is to initiate the method for frog meat identification using polymerase chain reaction (PCR) technique. In this study, three primer pairs (Fk1-Rk1, Fk2-Rk2, Fk3-Rk3) were analyzed for their specificity toward frog meat against other common halal meat sources such as beef, chicken, shrimp, squid, and mackerel. The visualization of DNA amplification showed that primer pair Fk1-Rk1 produced primer-dimer, thus cannot be used for this circumstance. Primer pair Fk2-Rk2 showed a better result where DNA amplicon was produced at ~100 bp for frog meat and no amplicons for other meat. Primer pair Fk3-Rk3 showed a different pattern of DNA amplification for all the meat tested, where the amplicon of frog meat was shown at ~100 bp, while the other meat showed multiple amplicons or none. In conclusion, primer pairs Fk2-Rk2 and Fk3-Rk3 showed their potential as primer pairs for frog meat identification using PCR for implementing halal food assurance, although sensitivity analysis needs to be investigated. Universitas Gadjah Mada, Indonesia 2023 Article PeerReviewed Haryono, Norman Yoshi and Khusufi, Rizqi Layli and Pangesti, Delia Wahyu and Susanti, Evi and Mariana, Rina Rifqie and Wardani, Hartati Eko and Salim, Norazlinaliza (2023) Primer pairs specificity test for frog meat identification using PCR technique. Indonesian Journal Of Chemistry, 23 (5). 1315 - 1323. ISSN 1411-9420; ESSN: 2460-1578 https://jurnal.ugm.ac.id/ijc/article/view/83626 10.22146/ijc.83626
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
description Halal food assurance is becoming more important with the growth of the halal industry globally. Adulteration of halal meat products using non-halal sources such as pork, dog, boar, and even frog meat has become a major problem for moslems. The purpose of this study is to initiate the method for frog meat identification using polymerase chain reaction (PCR) technique. In this study, three primer pairs (Fk1-Rk1, Fk2-Rk2, Fk3-Rk3) were analyzed for their specificity toward frog meat against other common halal meat sources such as beef, chicken, shrimp, squid, and mackerel. The visualization of DNA amplification showed that primer pair Fk1-Rk1 produced primer-dimer, thus cannot be used for this circumstance. Primer pair Fk2-Rk2 showed a better result where DNA amplicon was produced at ~100 bp for frog meat and no amplicons for other meat. Primer pair Fk3-Rk3 showed a different pattern of DNA amplification for all the meat tested, where the amplicon of frog meat was shown at ~100 bp, while the other meat showed multiple amplicons or none. In conclusion, primer pairs Fk2-Rk2 and Fk3-Rk3 showed their potential as primer pairs for frog meat identification using PCR for implementing halal food assurance, although sensitivity analysis needs to be investigated.
format Article
author Haryono, Norman Yoshi
Khusufi, Rizqi Layli
Pangesti, Delia Wahyu
Susanti, Evi
Mariana, Rina Rifqie
Wardani, Hartati Eko
Salim, Norazlinaliza
spellingShingle Haryono, Norman Yoshi
Khusufi, Rizqi Layli
Pangesti, Delia Wahyu
Susanti, Evi
Mariana, Rina Rifqie
Wardani, Hartati Eko
Salim, Norazlinaliza
Primer pairs specificity test for frog meat identification using PCR technique
author_facet Haryono, Norman Yoshi
Khusufi, Rizqi Layli
Pangesti, Delia Wahyu
Susanti, Evi
Mariana, Rina Rifqie
Wardani, Hartati Eko
Salim, Norazlinaliza
author_sort Haryono, Norman Yoshi
title Primer pairs specificity test for frog meat identification using PCR technique
title_short Primer pairs specificity test for frog meat identification using PCR technique
title_full Primer pairs specificity test for frog meat identification using PCR technique
title_fullStr Primer pairs specificity test for frog meat identification using PCR technique
title_full_unstemmed Primer pairs specificity test for frog meat identification using PCR technique
title_sort primer pairs specificity test for frog meat identification using pcr technique
publisher Universitas Gadjah Mada, Indonesia
publishDate 2023
url http://psasir.upm.edu.my/id/eprint/110064/
https://jurnal.ugm.ac.id/ijc/article/view/83626
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