DNA barcoding for the species identification of commercially important fishery products in Indonesian markets

被引:19
|
作者
Abdullah, Asadatun [1 ,2 ]
Rehbein, Hartmut [1 ]
机构
[1] Max Rubner Inst, Dept Safety & Qual Milk & Fish Prod, Palmaille 9, D-22767 Hamburg, Germany
[2] Bogor Agr Univ, Dept Aquat Prod Technol, Bogor, Indonesia
关键词
Adulteration; DNA analysis; fish; food quality; PCR analysis; GENETIC IDENTIFICATION; CYTOCHROME-B; AUTHENTICATION; SEAFOOD; FINS; REVEALS; TAIWAN; SUBSTITUTION; METHODOLOGY; SPARIDAE;
D O I
10.1111/ijfs.13278
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The DNA barcoding approach was used for the species identification of 44 Indonesian commercial fishery products. Additionally, the intronless nuclear rhodopsin gene fragment (RH1) was added to the analysis to enable the identification of species not yet barcoded and possible hybrids. The 655-bp cytochrome C oxidase subunit I (COI) gene fragment marker was successfully amplified and used to identify 86% of the total fish samples at the species level using the BOLD and BLAST public databases. Moreover, the RH1 marker was used to complete COI analysis. For a number of fish species, the COI sequences (six species) and RH1 sequences (eight species) were the first entries submitted to GenBank. This study demonstrated that COI barcoding is a promising tool for Indonesian fishery products and confirmed that it could be adopted in the future for regular seafood control as part of the Indonesian integrated food traceability system.
引用
收藏
页码:266 / 274
页数:9
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