National Research Centre on Meat, Chengicherla, Hyderabad 500092, India.
Department of Veterinary Public Health and Epidemiology, College of Veterinary Sciences, Hyderabad 500030, India.
Food Chem. 2017 Oct 15;233:311-320. doi: 10.1016/j.foodchem.2017.04.116. Epub 2017 Apr 21.
The present study compared the accuracy of an OFFGEL electrophoresis and tandem mass spectrometry-based proteomic approach with a DNA-based method for meat species identification from raw and cooked ground meat mixes containing cattle, water buffalo and sheep meat. The proteomic approach involved the separation of myofibrillar proteins using OFFGEL electrophoresis, SDS-PAGE and protein identification by MALDI-TOF MS. Species-specific peptides derived from myosin light chain-1 and 2 were identified for authenticating buffalo meat spiked at a minimum 0.5% level in sheep meat with high confidence. Relative quantification of buffalo meat mixed with sheep meat was done by quantitative label-free mass spectrometry using UPLC-QTOF and PLGS search engine to substantiate the confidence level of the data. In the DNA-based method, PCR amplification of mitochondrial D loop gene using species specific primers found 226bp and 126bp product amplicons for buffalo and cattle meat, respectively. The method was efficient in detecting a minimum of 0.5% and 1.0% when buffalo meat was spiked with cattle meat in raw and cooked meat mixes.
本研究比较了 OFFGEL 电泳和串联质谱蛋白质组学方法与基于 DNA 的方法在鉴定生肉和熟肉混合物中牛、水牛和羊肉种属的准确性。蛋白质组学方法涉及使用 OFFGEL 电泳、SDS-PAGE 分离肌球蛋白纤维蛋白,并用 MALDI-TOF MS 进行蛋白质鉴定。从肌球蛋白轻链-1 和 2 衍生的种属特异性肽用于鉴定在羊肉中以 0.5%最低水平掺入的水牛肉,鉴定结果具有高度可信度。使用 UPLC-QTOF 和 PLGS 搜索引擎进行无标记定量质谱相对定量,以证实数据的可信度。在基于 DNA 的方法中,使用种属特异性引物对线粒体 D 环基因进行 PCR 扩增,分别得到水牛和牛肉类的 226bp 和 126bp 产物扩增子。该方法在生肉和熟肉混合物中检测到 0.5%和 1.0%的水牛肉掺入时非常有效。