Molecular identification of Lutjanus species by PCR-RFLP analysis of mitochondrial 12S rRNA region

被引:3
作者
Sivaraman, Balasubramanian [1 ]
Jeyasekaran, Geevaretnam [1 ,2 ]
Shakila, Robinson Jeya [1 ]
Wilwet, Lidiya [1 ]
Alamelu, Venkatesan [1 ]
Aanand, Samraj [3 ]
Sukumar, Durairaj [4 ]
机构
[1] Tamil Nadu Dr J Jayalalithaa Fisheries Univ, Dept Fish Qual Assurance & Management, Fisheries Coll & Res Inst, Thoothukkudi, India
[2] Tamil Nadu Dr J Jayalalithaa Fisheries Univ, Nagapattinam, India
[3] Tamil Nadu Dr J Jayalalithaa Fisheries Univ, Erode Ctr Freshwater Aquaculture, Bhavanisagar, India
[4] Tamil Nadu Dr J Jayalalithaa Fisheries Univ, Dept Fish Proc Technol, Fisheries Coll & Res Inst, Thoothukkudi, India
关键词
Snappers; Authentication; 12S rRNA; PCR-RFLP; Endonucleases; DNA-BASED METHODS; SNAPPERS; AUTHENTICATION; FISH; SUBSTITUTION; SSCP; 16S;
D O I
10.1016/j.jfca.2019.103329
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A PCR-RFLP was developed by targeting the mitochondrial 12S rRNA region to authenticate the six species viz., Lutjanus fulvus, L. rivulatus, L. quinquelineatus, L. fulviflanuna, L. madras and L. decussatus available along the Indian coast. A newly designed primer set, 12SU-F/12SU-R, was used for PCR amplification to obtain a product size of 550 bp, which was then digested using three endonucleases viz., BseDI, MnlI and MspAll. All the six species were unambiguously differentiated by BseDI enzyme. MnlI differentiated only four species viz., L fulvus, L. quinquelineatus, L. fulvifiamma and L. madras; while MspAI differentiated four species viz., L. rivulatus, L. quinquelineatus, L. fulviflamma and L. madras from the rest. The developed PCR-RFLP protocol using BseDI enzyme can therefore be easily adopted by regulatory authorities to the prevention of possible adulteration of species for red snappers.
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页数:5
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