Determination of Cattle and Buffalo Skin Crackers Using Polymerase Chain Reaction Restriction Fragment Length Polymorphism

The aim of this study was to determine of cattle and buffalo species based on cytochrome b gene using PCR-RFLP. Cattle and buffalo hides were obtained from a slaughterhouse in Yogyakarta and Kudus Regency. To confirm the effectiveness and specificity of this fragment, there are seven of DNA mixture...

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Main Authors: Rulli Riana Dewi, Yuny Erwanto, Nanung Agus Fitriyanto
Format: Article
Language:Indonesian
Published: Universitas Gadjah Mada 2018-04-01
Series:Jurnal Sain Veteriner
Subjects:
Online Access:https://jurnal.ugm.ac.id/jsv/article/view/34667
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spelling doaj-6f695c125ee44aca8a7a0943b6a9e7222020-11-24T21:47:17ZindUniversitas Gadjah MadaJurnal Sain Veteriner0126-04212407-37332018-04-0135218419010.22146/jsv.3466720758Determination of Cattle and Buffalo Skin Crackers Using Polymerase Chain Reaction Restriction Fragment Length PolymorphismRulli Riana Dewi0Yuny Erwanto1Nanung Agus Fitriyanto2Fakultas Peternakan Universitas Gadjah MadaFakultas Peternakan Universitas Gadjah MadaFakultas Kedokteran Hewan Universitas Gadjah MadaThe aim of this study was to determine of cattle and buffalo species based on cytochrome b gene using PCR-RFLP. Cattle and buffalo hides were obtained from a slaughterhouse in Yogyakarta and Kudus Regency. To confirm the effectiveness and specificity of this fragment, there are seven of DNA mixture samples in various levels. Isolate DNA samples were amplified using universal primer of cytochrome b gene, then PCR amplicon was digested by RsaI restriction enzyme.. The result showed that mitochondrial cytochrome b gene successfully amplified fragments of 359 bp. RsaI restriction enzyme was able to cleave buffalo cytochrome b gene into two fragment  (326 and 23 bp), while the cytochrome b gene of the skin cattle DNA was uncleaved. . In conclusion, this study indicated that mixture DNA of cattle and buffalo hides could be digested by RsaI restriction enzyme  and determination of the buffalo hides in mixture samples could be detected into  10% level. Furthermore, RsaI enzyme could be used to specific identification buffalo species. PCR-RFLP technology has a potential and reliable method to identify  of the existence of r buffalo hides in the mixture with other hides.https://jurnal.ugm.ac.id/jsv/article/view/34667Cattle and buffalo hidesCytochrome bCrackersPolymerase chain reaction
collection DOAJ
language Indonesian
format Article
sources DOAJ
author Rulli Riana Dewi
Yuny Erwanto
Nanung Agus Fitriyanto
spellingShingle Rulli Riana Dewi
Yuny Erwanto
Nanung Agus Fitriyanto
Determination of Cattle and Buffalo Skin Crackers Using Polymerase Chain Reaction Restriction Fragment Length Polymorphism
Jurnal Sain Veteriner
Cattle and buffalo hides
Cytochrome b
Crackers
Polymerase chain reaction
author_facet Rulli Riana Dewi
Yuny Erwanto
Nanung Agus Fitriyanto
author_sort Rulli Riana Dewi
title Determination of Cattle and Buffalo Skin Crackers Using Polymerase Chain Reaction Restriction Fragment Length Polymorphism
title_short Determination of Cattle and Buffalo Skin Crackers Using Polymerase Chain Reaction Restriction Fragment Length Polymorphism
title_full Determination of Cattle and Buffalo Skin Crackers Using Polymerase Chain Reaction Restriction Fragment Length Polymorphism
title_fullStr Determination of Cattle and Buffalo Skin Crackers Using Polymerase Chain Reaction Restriction Fragment Length Polymorphism
title_full_unstemmed Determination of Cattle and Buffalo Skin Crackers Using Polymerase Chain Reaction Restriction Fragment Length Polymorphism
title_sort determination of cattle and buffalo skin crackers using polymerase chain reaction restriction fragment length polymorphism
publisher Universitas Gadjah Mada
series Jurnal Sain Veteriner
issn 0126-0421
2407-3733
publishDate 2018-04-01
description The aim of this study was to determine of cattle and buffalo species based on cytochrome b gene using PCR-RFLP. Cattle and buffalo hides were obtained from a slaughterhouse in Yogyakarta and Kudus Regency. To confirm the effectiveness and specificity of this fragment, there are seven of DNA mixture samples in various levels. Isolate DNA samples were amplified using universal primer of cytochrome b gene, then PCR amplicon was digested by RsaI restriction enzyme.. The result showed that mitochondrial cytochrome b gene successfully amplified fragments of 359 bp. RsaI restriction enzyme was able to cleave buffalo cytochrome b gene into two fragment  (326 and 23 bp), while the cytochrome b gene of the skin cattle DNA was uncleaved. . In conclusion, this study indicated that mixture DNA of cattle and buffalo hides could be digested by RsaI restriction enzyme  and determination of the buffalo hides in mixture samples could be detected into  10% level. Furthermore, RsaI enzyme could be used to specific identification buffalo species. PCR-RFLP technology has a potential and reliable method to identify  of the existence of r buffalo hides in the mixture with other hides.
topic Cattle and buffalo hides
Cytochrome b
Crackers
Polymerase chain reaction
url https://jurnal.ugm.ac.id/jsv/article/view/34667
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