A single enzyme PCR-RFLP protocol targeting 16S rRNA/tRNAval region to authenticate four commercially important shrimp species in India

被引:23
作者
Wilwet, Lidiya [1 ]
Jeyasekaran, Geevaretnam [1 ]
Shakila, Robinson Jeya [1 ]
Sivaraman, Balasubramanian [1 ]
Padmavathy, Pandurengan [2 ]
机构
[1] Tamil Nadu Fisheries Univ, Fisheries Coll & Res Inst, Dept Fish Qual Assurance & Management, Thoothukkudi 628008, India
[2] Tamil Nadu Fisheries Univ, Fisheries Coll & Res Inst, Dept Fisheries Environm, Thoothukkudi 628008, India
关键词
PCR-RFLP; mtDNA; Single enzyme; Penaeid shrimps; Species authentication; Seafood adulteration; FRAGMENT LENGTH POLYMORPHISM; DNA-BASED METHODS; RIBOSOMAL-RNA; MOLECULAR-IDENTIFICATION; MITOCHONDRIAL REGION; GENE FRAGMENT; FOOD INTEREST; PENAEUS; PENAEOIDEA; VANNAMEI;
D O I
10.1016/j.foodchem.2017.06.132
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Food authenticity is an issue of major concern for food authorities, as mislabeling represents one of the major commercial frauds. In this study, a novel PCR-RFLP protocol was developed as a tool to authenticate four shrimp products of commercial importance belonging to the family, Penaeidae, viz. Litopenaeus vannamei, Penaeus monodon, P. semisulcatus and Fenneropenaeus indicus. PCR amplification was performed targeting 16S rRNA/tRNA(val) region having an amplicon size of 530 bp using the specific primers for shrimps, 16S-Cru4/16S-Cru3. Subsequent restriction analysis with a single restriction enzyme, Tsp5091, yielded distinct RFLP pattern for each species of shrimps having fragment sizes below 150 bp. The unique RFLP patterns were also obtained in processed shrimp products without any degradation or alteration in the major fragments. The method was also validated with commercial shrimp products. Thus, the developed protocol can be performed within 8 h using a single enzyme to authenticate four shrimp products of commercial significance. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:369 / 376
页数:8
相关论文
共 25 条
[1]  
Angelica L., 2014, EXPLORATORY SURVEY F, V62, P104
[2]  
[Anonymous], AUTHENTICITY SPECIES
[3]   Molecular characterization of icefish, (Salangidae family), using direct sequencing of mitochondrial cytochrome b gene [J].
Armani, Andrea ;
Castigliego, Lorenzo ;
Tinacci, Lara ;
Gianfaldoni, Daniela ;
Guidi, Alessandra .
FOOD CONTROL, 2011, 22 (06) :888-895
[4]   Molecular phylogeny and biogeography of the marine shrimp Penaeus [J].
Baldwin, JD ;
Bass, AL ;
Bowen, BW ;
Clark, WH .
MOLECULAR PHYLOGENETICS AND EVOLUTION, 1998, 10 (03) :399-407
[5]   Detection of crustacean DNA and species identification using a PCR-restriction fragment length polymorphism method [J].
Brzezinski, JL .
JOURNAL OF FOOD PROTECTION, 2005, 68 (09) :1866-1873
[6]   Evaluation of a novel 16S rRNA/tRNAVal mitochondrial marker for the identification and phylogenetic analysis of shrimp species belonging to the superfamily Penaeoidea [J].
Calo-Mata, Pilar ;
Pascoal, Ananias ;
Fernandez-No, Inmaculada ;
Boehme, Karola ;
Gallardo, Jose M. ;
Barros-Velazquez, Jorge .
ANALYTICAL BIOCHEMISTRY, 2009, 391 (02) :127-134
[7]  
Céspedes A, 2000, J SCI FOOD AGR, V80, P29, DOI 10.1002/(SICI)1097-0010(20000101)80:1<29::AID-JSFA470>3.0.CO
[8]  
2-4
[9]   Genetic stock structure of the swordfish (Xiphias gladius) inferred by PCR-RFLP analysis of the mitochondrial DNA control region [J].
Chow, S ;
Okamoto, H ;
Uozumi, Y ;
Takeuchi, Y ;
Takeyama, H .
MARINE BIOLOGY, 1997, 127 (03) :359-367
[10]   SNP-based PCR-RFLP, T-RFLP and FINS methodologies for the identification of commercial fish species in Egypt [J].
Galal-Khallaf, Asmaa ;
Mohammed-Geba, Khaled ;
Osman, Alaa G. M. ;
AbouelFadl, Khaled Y. ;
Borrell, Yaisel J. ;
Garcia-Vazquez, Eva .
FISHERIES RESEARCH, 2017, 185 :34-42