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聚合酶链反应检测试剂盒针对细胞色素 b 基因检测肉丸中的狗肉掺假。

Polymerase chain reaction assay targeting cytochrome b gene for the detection of dog meat adulteration in meatball formulation.

机构信息

Nanotechnology and Catalysis Research Centre, Universiti Malaya, Kuala Lumpur 50603, Malaysia.

Nanotechnology and Catalysis Research Centre, Universiti Malaya, Kuala Lumpur 50603, Malaysia.

出版信息

Meat Sci. 2014 Aug;97(4):404-9. doi: 10.1016/j.meatsci.2014.03.011. Epub 2014 Mar 26.

Abstract

A polymerase chain reaction (PCR) assay for the assessment of dog meat adulteration in meatballs was developed. The assay selectively amplified a 100-bp region of canine mitochondrial cytochrome b gene from pure, raw, processed and mixed backgrounds. The specificity of the assay was tested against 11 animals and 3 plants species, commonly available for meatball formulation. The stability of the assay was proven under extensively autoclaving conditions that breakdown target DNA. A blind test from ready to eat chicken and beef meatballs showed that the assay can repeatedly detect 0.2% canine meat tissues under complex matrices using 0.04 ng of dog DNA extracted from differentially treated meatballs. The simplicity, stability and sensitivity of the assay suggested that it could be used in halal food industry for the authentication of canine derivatives in processed foods.

摘要

建立了一种用于评估肉丸中狗肉掺假的聚合酶链反应(PCR)检测方法。该方法可选择性地扩增来自纯、生、加工和混合背景的犬线粒体细胞色素 b 基因的 100bp 区域。该方法的特异性已针对 11 种动物和 3 种植物物种进行了测试,这些物种通常可用于制作肉丸。该方法在广泛的高压灭菌条件下具有稳定性,这种条件会破坏目标 DNA。对即食鸡肉和牛肉肉丸进行的盲测表明,该方法可在复杂基质中使用从不同处理的肉丸中提取的 0.04ng 犬 DNA,反复检测到 0.2%的犬肉组织。该检测方法的简单性、稳定性和敏感性表明,它可用于清真食品行业,用于鉴定加工食品中的犬类衍生物。

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