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วารสารเทคโนโลยีชีวภาพการผลิตปศุสัตว์
Introduction
Species identification of animal product using molecular technology is currently an important
issue for food authenticity since incorrect labeling of origin may have negative consequences such
as food allergy, religion aspect, and illegal mixed cheaper meat to the products, etc. (Ghovvati et
al., 2009). Species detection is also involved in wildlife management in order to define the animal
species (Li-Chin Tsai et al., 2007) which endangered species are illegally killed. Both food
authentication and protection of biodiversity require reliable and accurate methods for determining.
Moreover, species identification is one of significant steps in the genetic traceability system of food
process (Hobbs, 2004; Smith et al., 2005; Schwagele, 2005). Recently, many studies focused on
the development of DNA based technology to differentiate the species of the animals (Bottero et al.,
2003; Dalmasso et al., 2004) including the advantage of Polymerase Chain Reaction (PCR)
technology. PCR method can be used to amplify small amount of specific DNA target sequences in
a short period of time faster than other methods such as polypeptide identification or protein analysis
including electrophoretic, immunological, mass-spectrometric and chromatographic techniques since
the protein will degrade rapidly after animal died or being cooked. (Gouli et al., 1999). Among of
selected genes, Cytochrome b (cyt b) gene, one of the most mitochondrial (mt) genes which differs
five- to tenfold of DNA copies higher than nuclear genes, is used for identifying animal species. This
gene is found in all vertebrates and does not undergo recombination, enables closely related species
to be differentiated and identified (Matsuda et al., 2005). Kocher et al. (1989) reported universal
primers which could be used to amplify a wide range of vertebrate species. Although these
researches had been done on several kinds of animals, there was no report of animal species
identification using multiplex PCR technique that included the 6 animal species which were targeted
in this study.
The purpose of this study is to develop a molecular method, based on cyt b gene, multiplex
PCR technique to identify the 6 species of animals (cattle, buffalo, goat, sheep, chicken and pig) as
mainly food source in Thailand.
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