Forgery Detection Beef with Mice Meat (<i>Mus musculus</i>) in Meatballs Using Real-Time Polymerase Chain Reaction (Real-Time PCR) Primer Specific for a Target Mitochondrial DNA ND-1 Gene

The expensive beef have encouraged counterfeiting beef on processed food products such as meatballs. Mice meat is frequently reported used for adulteration of beef. The accurate method is needed to ensure the supervision of food safety. This study reports the use of DNA testing to detect the presenc...

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Main Authors: Tri Joko Raharjo, Gilang Aji Pratama, Irma Nuryanti, Rarastoeti Pratiwi
Format: Article
Language:English
Published: Universitas Gadjah Mada 2019-01-01
Series:Indonesian Journal of Chemistry
Subjects:
Online Access:https://jurnal.ugm.ac.id/ijc/article/view/27542
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spelling doaj-24f2ff19666644e9959378e73960cd482020-11-24T21:05:59ZengUniversitas Gadjah MadaIndonesian Journal of Chemistry1411-94202460-15782019-01-01191899610.22146/ijc.2754221931Forgery Detection Beef with Mice Meat (<i>Mus musculus</i>) in Meatballs Using Real-Time Polymerase Chain Reaction (Real-Time PCR) Primer Specific for a Target Mitochondrial DNA ND-1 GeneTri Joko Raharjo0Gilang Aji Pratama1Irma Nuryanti2Rarastoeti Pratiwi3Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281, IndonesiaBiotechnology Study Program, Graduated School, Universitas Gadjah Mada, YogyakartaDexa Laboratories of Biomolecular Sciences, Cikarang, Bekasi 17530, West Java, IndonesiaFaculty of Biology, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281, IndonesiaThe expensive beef have encouraged counterfeiting beef on processed food products such as meatballs. Mice meat is frequently reported used for adulteration of beef. The accurate method is needed to ensure the supervision of food safety. This study reports the use of DNA testing to detect the presence of mice meat in meatballs with real-time PCR primer specific. PCR primers designed based on the ND-1 gene of mice mitochondrial DNA with the sequence are 5’-CGGCATCCTACAACCATTTGC-3’ and 5’-CGGCTCGTAAAGCTCCGAA-3’, respectively, target 294 bp DNA fragment. The real-time PCR can specifically detect the presence of the mice meat in a meatball with no detection the presence of beef, mutton, chicken, pork, and horsemeat. The method showed good precision shown by the CV of repeatability test at 2%, much lower than the requirement of < 25%. Real-time PCR was able to deliver positive results for as low as 0.5 ng DNA template, equivalent to 0.08 copies of genome DNA of mice equal to 80–150 copies of mtDNA. By using standard phenol-chloroform DNA isolation technique, this method is able to detect contamination of mice meat in meatball up to 1%. Three commercial meatballs confirmed contaminated by mice meat using the method.https://jurnal.ugm.ac.id/ijc/article/view/27542micemeatballreal-time PCRND-1mitochondrial DNA
collection DOAJ
language English
format Article
sources DOAJ
author Tri Joko Raharjo
Gilang Aji Pratama
Irma Nuryanti
Rarastoeti Pratiwi
spellingShingle Tri Joko Raharjo
Gilang Aji Pratama
Irma Nuryanti
Rarastoeti Pratiwi
Forgery Detection Beef with Mice Meat (<i>Mus musculus</i>) in Meatballs Using Real-Time Polymerase Chain Reaction (Real-Time PCR) Primer Specific for a Target Mitochondrial DNA ND-1 Gene
Indonesian Journal of Chemistry
mice
meatball
real-time PCR
ND-1
mitochondrial DNA
author_facet Tri Joko Raharjo
Gilang Aji Pratama
Irma Nuryanti
Rarastoeti Pratiwi
author_sort Tri Joko Raharjo
title Forgery Detection Beef with Mice Meat (<i>Mus musculus</i>) in Meatballs Using Real-Time Polymerase Chain Reaction (Real-Time PCR) Primer Specific for a Target Mitochondrial DNA ND-1 Gene
title_short Forgery Detection Beef with Mice Meat (<i>Mus musculus</i>) in Meatballs Using Real-Time Polymerase Chain Reaction (Real-Time PCR) Primer Specific for a Target Mitochondrial DNA ND-1 Gene
title_full Forgery Detection Beef with Mice Meat (<i>Mus musculus</i>) in Meatballs Using Real-Time Polymerase Chain Reaction (Real-Time PCR) Primer Specific for a Target Mitochondrial DNA ND-1 Gene
title_fullStr Forgery Detection Beef with Mice Meat (<i>Mus musculus</i>) in Meatballs Using Real-Time Polymerase Chain Reaction (Real-Time PCR) Primer Specific for a Target Mitochondrial DNA ND-1 Gene
title_full_unstemmed Forgery Detection Beef with Mice Meat (<i>Mus musculus</i>) in Meatballs Using Real-Time Polymerase Chain Reaction (Real-Time PCR) Primer Specific for a Target Mitochondrial DNA ND-1 Gene
title_sort forgery detection beef with mice meat (<i>mus musculus</i>) in meatballs using real-time polymerase chain reaction (real-time pcr) primer specific for a target mitochondrial dna nd-1 gene
publisher Universitas Gadjah Mada
series Indonesian Journal of Chemistry
issn 1411-9420
2460-1578
publishDate 2019-01-01
description The expensive beef have encouraged counterfeiting beef on processed food products such as meatballs. Mice meat is frequently reported used for adulteration of beef. The accurate method is needed to ensure the supervision of food safety. This study reports the use of DNA testing to detect the presence of mice meat in meatballs with real-time PCR primer specific. PCR primers designed based on the ND-1 gene of mice mitochondrial DNA with the sequence are 5’-CGGCATCCTACAACCATTTGC-3’ and 5’-CGGCTCGTAAAGCTCCGAA-3’, respectively, target 294 bp DNA fragment. The real-time PCR can specifically detect the presence of the mice meat in a meatball with no detection the presence of beef, mutton, chicken, pork, and horsemeat. The method showed good precision shown by the CV of repeatability test at 2%, much lower than the requirement of < 25%. Real-time PCR was able to deliver positive results for as low as 0.5 ng DNA template, equivalent to 0.08 copies of genome DNA of mice equal to 80–150 copies of mtDNA. By using standard phenol-chloroform DNA isolation technique, this method is able to detect contamination of mice meat in meatball up to 1%. Three commercial meatballs confirmed contaminated by mice meat using the method.
topic mice
meatball
real-time PCR
ND-1
mitochondrial DNA
url https://jurnal.ugm.ac.id/ijc/article/view/27542
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