Species identification in salted products of red snappers by semi-nested PCR–RFLP based on the mitochondrial 12S rRNA gene sequence

Food Control ◽  
2007 ◽  
Vol 18 (11) ◽  
pp. 1331-1336 ◽  
Author(s):  
Junbin Zhang ◽  
Hui Huang ◽  
Zeping Cai ◽  
Liangmin Huang
2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Chandra Mohan Siddappa ◽  
Mohini Saini ◽  
Asit Das ◽  
Ramesh Doreswamy ◽  
Anil K. Sharma ◽  
...  

Mitochondrial 12S rRNA has proven to be a useful molecular marker for better conservation and management of the endangered species. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) of the mitochondrial 12S rRNA gene has proven to be a reliable and efficient tool for the identification of different Indian deer species of family cervidae. In the present study, mitochondrial 12S rRNA gene sequence of mouse deer (Moschiola indica) belonging to the family Tragulidae was characterized and analysed in silico for its use in species identification. Genomic DNA was isolated from the hair follicles and mitochondrial 12S rRNA gene was amplified using universal primers. PCR product was cloned and sequenced for the first time. The sequence of mouse deer showed 90.04, 90.08, 90.04, 91.2, 90.04, and 90.08% identities with sika deer, sambar, hog deer, musk deer, chital, and barking deer, respectively. Restriction mapping in Lasergene (DNAstar Inc., Madison, WI, USA) revealed that mouse deer mitochondrial 12S rRNA gene sequence can be differentiated from the other deer species in PCR-RFLP using RsaI, DdeI, BsrI, and BstSFI. With the help of predicted pattern, mouse deer can be identified using genomic DNA from a variety of biomaterials, thereby providing molecular aid in wildlife forensics and conservation of the species.


2003 ◽  
Vol 1239 ◽  
pp. 75-78
Author(s):  
C Albarrán ◽  
P Martı́n ◽  
O Garcı́a ◽  
P Garcı́a ◽  
L Fernández de Simón ◽  
...  

2005 ◽  
Vol 119 (5) ◽  
pp. 291-294 ◽  
Author(s):  
B. Balitzki-Korte ◽  
K. Anslinger ◽  
C. Bartsch ◽  
B. Rolf

2020 ◽  
Vol 23 ◽  
Author(s):  
Josué Tafur-Culqui ◽  
Martha S. Calderon ◽  
Danilo E. Bustamante

Abstract The use of analytical methodologies based on DNA (e.g. PCR-RFLP) to determine the authenticity of different types of meat products after the initial labeling is pivotal to avoid fraudulent practices due to the increased rates of meat consumption. Our PCR-RFLP of mitochondrial 12S rRNA gene using restriction enzymes (AluI and ApoI) aimed to confirm the accuracy of the meat species labeling, based on fresh and processed meat collected in central markets along the main cities in the Amazonas Region (Bagua, Bagua Grande, Chachapoyas, Luya, Pedro Ruiz, Rodriguez de Mendoza). Our analyses qualitatively identified and differentiated three commercial species of fresh meat (bovine, porcine, ovine) and also found the substitution of goat by sheep meat. Regarding processed meat, its composition was uncertain and further analyses should be addressed to determine the meat origin. Monitoring using DNA-based analytical methods of meat trade is suggested to determine fraudulent practices, such as species substitution in markets along regions of Peru.


2007 ◽  
Vol 27 (2) ◽  
pp. 209-215 ◽  
Author(s):  
Jong-Keun Park ◽  
Ki-Hyun Shin ◽  
Sung-Chul Shin ◽  
Ku-Young Chung ◽  
Eui-Ryong Chung

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