Multiplex PCR in Species Authentication: Probability and Prospects-A Review

被引:97
作者
Ali, Md. Eaqub [1 ,2 ]
Razzak, Md. Abdur [1 ]
Abd Hamid, Sharifah Bee [1 ]
机构
[1] Univ Malaya, Nanotechnol & Catalysis Res Ctr NanoCat, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Ctr Res Biotechnol Agr CEBAR, Kuala Lumpur 50603, Malaysia
关键词
Food forgery; Lipid; Protein- and DNA-based biomarkers; Multiplex PCR; REAL-TIME PCR; POLYMERASE-CHAIN-REACTION; CYTOCHROME-B GENE; LINKED-IMMUNOSORBENT-ASSAY; PROCESSED ANIMAL PROTEINS; MEAT-PRODUCTS; QUANTITATIVE PCR; HALAL AUTHENTICATION; RAPID IDENTIFICATION; DNA IDENTIFICATION;
D O I
10.1007/s12161-014-9844-4
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Food forgery is one of the most articulated socioeconomic concerns which contributed to increase people's awareness on what they eat and how and where it is produced. Consumers are anxious about the consequences of food falsification on their choices, religious rituals, health, and hard-earned fortunes. The recent scandals of horse and rat meats in Europe and China have given us a brainstorming apprehension on the detection, differentiation, and identification of meat products. To restore consumers' trust and protect wildlife in natural habitats, researchers and policy-making and policy-implementing authorities have massively monitored all steps in the production of foods and food materials. Analytical approaches based on lipids, proteins, and DNA have been proposed for the authentication of meat species under pure and complex matrices. However, protein and lipid-based methods are less effective since the target biomarkers could be modified throughout the processing treatments. On the other hand, DNA-based species identification schemes have gained wider acceptance and reliability because of the superior stability and universality of DNA in all tissues and cells. We systematically presented here major species detection schemes with special emphasis on multiplex polymerase chain reaction (PCR) of both end-point and real-time platforms. We believe this short but comprehensive review would serve as a reference guide for the developers and users of multiplex PCR and others DNA-based techniques.
引用
收藏
页码:1933 / 1949
页数:17
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