Polymerase chain reaction-restriction fragment length polymorphism analysis of a 16S rRNA gene fragment for authentication of four clam species

被引:12
|
作者
Fernández, A [1 ]
García, T [1 ]
González, I [1 ]
Asensio, L [1 ]
Rodríguez, MA [1 ]
Hernández, PE [1 ]
Martín, R [1 ]
机构
[1] Univ Complutense Madrid, Fac Vet, Dept Nutr & Bromatol 3, E-28040 Madrid, Spain
关键词
D O I
10.4315/0362-028X-65.4.692
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Specific identification of four clam species, Ruditapes decussates (grooved carpet shell), Venerupis pullastra (pullet carpet shell), Ruditapes philippinarum (Japanese carpet shell), and Venerupis rhomboides (yellow carpet shell), was achieved by polymerase chain reaction-restriction fragment length polymorphism analysis of a fragment of the mitochondrial 16S rRNA gene. Amplification of DNA isolated from the foot muscle produced fragments of 511 by for V. pullastra, 523 by for R. decussatus, 545 by for R. philippinarum, and 502 by for V rhomboides. The restriction profiles obtained by agarose gel electrophoresis when amplicons were digested with endonucleases BsmAI and BsrI allowed unequivocal identification of the four clam species. This approach would be less costly, simpler, and quicker than conventional sequencing of polymerase chain reaction products followed by detailed comparison of individual sequences, especially when large numbers of samples need to be analyzed.
引用
收藏
页码:692 / 695
页数:4
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