Development of RAPD-PCR assay for identifying Holstein, Angus, and Taiwan Yellow Cattle for meat adulteration detection

Incidents of food fraud have occurred worldwide, particularly in the form of meat adulteration. In this study, molecular probes were developed using the Random amplification of polymorphic DNA (RAPD) polymerase chain reaction (PCR) technique in order to identify three beef subspecies–Holstein, Angus...

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Published inFood science and biotechnology Vol. 28; no. 6; pp. 1769 - 1777
Main Authors Lin, Chin-Cheng, Tang, Pin-Chi, Chiang, Hsin-I
Format Journal Article
LanguageEnglish
Published Singapore Springer Singapore 01.12.2019
Springer Nature B.V
한국식품과학회
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Abstract Incidents of food fraud have occurred worldwide, particularly in the form of meat adulteration. In this study, molecular probes were developed using the Random amplification of polymorphic DNA (RAPD) polymerase chain reaction (PCR) technique in order to identify three beef subspecies–Holstein, Angus, and Taiwan Yellow Cattle. Four RAPD-PCR 10-nucleotide primers were chosen out of a total of 60 primers. The selection was based on the reproducibility of species-specific amplicons able to detect various origins of cattle breeds. The results demonstrated that primer OPK12 produced three unique amplicons (1100 bp, 1000 bp and 480 bp) in Holstein; primer OPK14 generated one amplicon that only appeared in Holstein and Angus (200 bp); primer OPK19 amplified two species-specific amplicons in Holstein measuring 550 bp and 650 bp, respectively. However, due to the relatively lower repeatability of RAPD-PCR, higher and more specific testing repeats were required to increase the accuracy of the conclusion.
AbstractList Incidents of food fraud have occurred worldwide, particularly in the form of meat adulteration. In this study, molecular probes were developed using the Random amplification of polymorphic DNA (RAPD) polymerase chain reaction (PCR) technique in order to identify three beef subspecies–Holstein, Angus, and Taiwan Yellow Cattle. Four RAPD-PCR 10-nucleotide primers were chosen out of a total of 60 primers. The selection was based on the reproducibility of species-specific amplicons able to detect various origins of cattle breeds. The results demonstrated that primer OPK12 produced three unique amplicons (1100 bp, 1000 bp and 480 bp) in Holstein; primer OPK14 generated one amplicon that only appeared in Holstein and Angus (200 bp); primer OPK19 amplified two species-specific amplicons in Holstein measuring 550 bp and 650 bp, respectively. However, due to the relatively lower repeatability of RAPD-PCR, higher and more specific testing repeats were required to increase the accuracy of the conclusion.
Incidents of food fraud have occurred worldwide, particularly in the form of meat adulteration. In this study, molecular probes were developed using the Random amplification of polymorphic DNA (RAPD) polymerase chain reaction (PCR) technique in order to identify three beef subspecies-Holstein, Angus, and Taiwan Yellow Cattle. Four RAPD-PCR 10-nucleotide primers were chosen out of a total of 60 primers. The selection was based on the reproducibility of species-specific amplicons able to detect various origins of cattle breeds. The results demonstrated that primer OPK12 produced three unique amplicons (1100 bp, 1000 bp and 480 bp) in Holstein; primer OPK14 generated one amplicon that only appeared in Holstein and Angus (200 bp); primer OPK19 amplified two species-specific amplicons in Holstein measuring 550 bp and 650 bp, respectively. However, due to the relatively lower repeatability of RAPD-PCR, higher and more specific testing repeats were required to increase the accuracy of the conclusion.Incidents of food fraud have occurred worldwide, particularly in the form of meat adulteration. In this study, molecular probes were developed using the Random amplification of polymorphic DNA (RAPD) polymerase chain reaction (PCR) technique in order to identify three beef subspecies-Holstein, Angus, and Taiwan Yellow Cattle. Four RAPD-PCR 10-nucleotide primers were chosen out of a total of 60 primers. The selection was based on the reproducibility of species-specific amplicons able to detect various origins of cattle breeds. The results demonstrated that primer OPK12 produced three unique amplicons (1100 bp, 1000 bp and 480 bp) in Holstein; primer OPK14 generated one amplicon that only appeared in Holstein and Angus (200 bp); primer OPK19 amplified two species-specific amplicons in Holstein measuring 550 bp and 650 bp, respectively. However, due to the relatively lower repeatability of RAPD-PCR, higher and more specific testing repeats were required to increase the accuracy of the conclusion.
Incidents of food fraud have occurred worldwide, particularly in the form of meat adulteration. In this study, molecular probes were developed using the Random amplification of polymorphic DNA (RAPD) polymerase chain reaction (PCR) technique in order to identify three beef subspecies-Holstein, Angus, and Taiwan Yellow Cattle. Four RAPD-PCR 10-nucleotide primers were chosen out of a total of 60 primers. The selection was based on the reproducibility of species-specific amplicons able to detect various origins of cattle breeds. The results demonstrated that primer OPK12 produced three unique amplicons (1100 bp, 1000 bp and 480 bp) in Holstein; primer OPK14 generated one amplicon that only appeared in Holstein and Angus (200 bp); primer OPK19 amplified two species-specific amplicons in Holstein measuring 550 bp and 650 bp, respectively. However, due to the relatively lower repeatability of RAPD-PCR, higher and more specific testing repeats were required to increase the accuracy of the conclusion.
Incidents of food fraud have occurred worldwide,particularly in the form of meat adulteration. In thisstudy, molecular probes were developed using the Randomamplification of polymorphic DNA (RAPD) polymerasechain reaction (PCR) technique in order to identify threebeef subspecies–Holstein, Angus, and Taiwan YellowCattle. Four RAPD-PCR 10-nucleotide primers were chosenout of a total of 60 primers. The selection was based onthe reproducibility of species-specific amplicons able todetect various origins of cattle breeds. The resultsdemonstrated that primer OPK12 produced three uniqueamplicons (1100 bp, 1000 bp and 480 bp) in Holstein;primer OPK14 generated one amplicon that only appearedin Holstein and Angus (200 bp); primer OPK19 amplifiedtwo species-specific amplicons in Holstein measuring550 bp and 650 bp, respectively. However, due to therelatively lower repeatability of RAPD-PCR, higher andmore specific testing repeats were required to increase theaccuracy of the conclusion. KCI Citation Count: 7
Author Tang, Pin-Chi
Chiang, Hsin-I
Lin, Chin-Cheng
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Keywords Food adulteration
RAPD-PCR
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Species identification
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Snippet Incidents of food fraud have occurred worldwide, particularly in the form of meat adulteration. In this study, molecular probes were developed using the Random...
Incidents of food fraud have occurred worldwide,particularly in the form of meat adulteration. In thisstudy, molecular probes were developed using the...
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SubjectTerms adulterated products
Amplification
Angus
beef
Beef cattle
biotechnology
Cattle
Chemistry
Chemistry and Materials Science
DNA
DNA probes
food fraud
Food Science
Fraud
Holstein
Meat
Nucleotides
Nutrition
Polymerase chain reaction
Random amplified polymorphic DNA
random amplified polymorphic DNA technique
Reproducibility
Taiwan
식품과학
Title Development of RAPD-PCR assay for identifying Holstein, Angus, and Taiwan Yellow Cattle for meat adulteration detection
URI https://link.springer.com/article/10.1007/s10068-019-00607-7
https://www.ncbi.nlm.nih.gov/pubmed/31807349
https://www.proquest.com/docview/2315143566
https://www.proquest.com/docview/2322750946
https://www.proquest.com/docview/2524308572
https://pubmed.ncbi.nlm.nih.gov/PMC6859182
https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002532981
Volume 28
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