2021
DOI: 10.1080/07388551.2021.1874279
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DNA barcoding: a modern age tool for detection of adulteration in food

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Cited by 61 publications
(25 citation statements)
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“…However, the standardization of the methodology to be used for species identification is also pivotal to face the food safety and quality concerns in a global food market. In this regard, the DNA based technologies have proven to be very effective as food fraud detection tools [ 13 , 14 ] and the methodology of DNA barcoding based on the cytochrome oxidase I sequences is the most used one [ 12 , 33 , 34 , 35 , 79 ]. In the last decade new techniques such as Real Time-PCR, Single Nucleotide Polymorphisms (SNPs), Forensically Informative Nucleotide Sequencing (FINS), Loop-mediated isothermal amplification (LAMP), Droplet Digital PCR (ddPCR), High Resolution Melting Analysis (HRMA), Next Generation Sequencing (NGS) metabarcoding, have been proposed by researchers with the aim of optimizing time, costs and effectiveness of species authentication in multi-species fish products [ 80 , 81 , 82 , 83 ].…”
Section: Discussionmentioning
confidence: 99%
“…However, the standardization of the methodology to be used for species identification is also pivotal to face the food safety and quality concerns in a global food market. In this regard, the DNA based technologies have proven to be very effective as food fraud detection tools [ 13 , 14 ] and the methodology of DNA barcoding based on the cytochrome oxidase I sequences is the most used one [ 12 , 33 , 34 , 35 , 79 ]. In the last decade new techniques such as Real Time-PCR, Single Nucleotide Polymorphisms (SNPs), Forensically Informative Nucleotide Sequencing (FINS), Loop-mediated isothermal amplification (LAMP), Droplet Digital PCR (ddPCR), High Resolution Melting Analysis (HRMA), Next Generation Sequencing (NGS) metabarcoding, have been proposed by researchers with the aim of optimizing time, costs and effectiveness of species authentication in multi-species fish products [ 80 , 81 , 82 , 83 ].…”
Section: Discussionmentioning
confidence: 99%
“…DNA barcoding provides a way to confirm the authentication of plants and establish a level of quality assurance within the market [ 52 , 53 , 54 , 55 , 56 , 57 , 58 , 59 ]. Since the first DNA barcoding study [ 60 ], the “animal barcode”, a portion of the mitochondrial gene cytochrome oxidase 1( CO 1), has proved remarkably effective at discriminating among species in diverse groups, such as birds, fishes, and insects [ 60 , 61 ].…”
Section: Introductionmentioning
confidence: 99%
“…The ITS primers, ITS1 and ITS4 [ 86 ] were originally designed for fungi and found useful to detect fungal contamination in herbal plant samples [ 87 , 88 , 89 , 90 ].Sequences of 18S, 5.8S and 26S rDNA are highly conserved from bacteria, fungi and higher plants, enabling the design of the sequence-complemented universal primers for PCR amplification of ITS [ 91 ] across the kingdoms. To improve the quality of ITS sequence information in DNA-barcoding, there are plant-specific ITS primers that can avoid preferential amplification of fungal contaminants or non-plants templates [ 59 , 88 , 92 , 93 ]. Due to the decreased length of the ITS2 sequence (<300 bp), it has been proposed as a suitable for DNA barcoding applications in plants [ 68 , 94 , 95 , 96 , 97 ].There are issues, such as paralogy and polymorphic sites, with the ITS repeats [ 61 , 98 ] that make some taxonomists wary of using them, but for authentication purposes, ITS (and particularly ITS2) have advantages that tend to outweigh these issues.…”
Section: Introductionmentioning
confidence: 99%
“…In recent years, remarkable progress has been made towards developing DNA barcoding and DNA metabarcoding methods for food authentication [19][20][21][22][23]. DNA barcoding is based on amplification of short DNA barcode regions, followed by either high resolution melting (HRM) analysis [24,25] or Sanger sequencing [26,27].…”
Section: Introductionmentioning
confidence: 99%