Real-time PCR in Food Science: PCR Diagnostics

被引:34
|
作者
Rodriguez-Lazaro, David [1 ]
Cook, Nigel [2 ]
Hernandez, Marta [3 ]
机构
[1] Univ Burgos, Microbiol Sect, Burgos, Spain
[2] FERA, York, N Yorkshire, England
[3] Inst Tecnol Agr Castilla & Leon ITACyL, Valladolid, Spain
关键词
LISTERIA-MONOCYTOGENES; DEAD CELLS; CAMPYLOBACTER-JEJUNI; ETHIDIUM MONOAZIDE; DNA; AMPLIFICATION; INHIBITION; ILLNESS; DIFFERENTIATION; QUANTIFICATION;
D O I
10.21775/cimb.015.039
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A principal consumer demand is a guarantee of the safety and quality of food. The presence of foodborne pathogens and their potential hazard, the use of genetically modified organisms (GMOs) in food production, and the correct labelling in foods suitable for vegetarians are among the subjects where society demands total transparency. The application of controls within the quality assessment programmes of the food industry is a way to satisfy these demands, and is necessary to ensure efficient analytical methodologies are possessed and correctly applied by the Food Sector. The use of real-time PCR has become a promising alternative approach in food diagnostics. It possesses a number of advantages over conventional culturing approaches, including rapidity, excellent analytical sensitivity and selectivity, and potential for quantification. However, the use of expensive equipment and reagents, the need for qualified personnel, and the lack of standardized protocols are impairing its practical implementation for food monitoring and control.
引用
收藏
页码:39 / 43
页数:5
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