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首页> 外文期刊>Asian Journal of Microbiology, Biotechnology and Environmental Science >DEVELOPMENT OF HIGH THROUGHPUT REAL-TIME PCR ARRAY TECHNIQUE FOR SCREENING OF FOOD SAMPLES FOR MYCOTOXIN PRODUCING FUNGI CONTAMINATION
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DEVELOPMENT OF HIGH THROUGHPUT REAL-TIME PCR ARRAY TECHNIQUE FOR SCREENING OF FOOD SAMPLES FOR MYCOTOXIN PRODUCING FUNGI CONTAMINATION

机译:高通量实时PCR阵列技术筛选真菌毒素产生的食品中真菌污染的研究。

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摘要

A high throughput PCR array technique has been developed for the simultaneous detection of several mycotoxin-producing fungi by using Real - Time PCR. The primers were designed based on the key genes involved in the different mycotoxin producing biosynthetic pathway of aflatoxin, Patulin, Trichothecene, Fumonisins and Ochratoxin A with a uniform Tm (Melting Temperature) to use in a single array simultaneously. These primers were arranged in an array form for the simultaneous detection of 14 mycotoxin-producing fungi in a single reaction set up. The method was validated by using the standard authentic DNA isolated from different mycotoxin producing fungi and real - Time PCR was performed by using SYBR Green 1 fluorescent dye method. The validated protocol was employed for screening the commercially available food samples by using the DNA isolated from the collected food samples. The results from these studies have shown that several commercially available food samples are contaminated with mycotoxinproducing fungi. Thus this high throughput Real - Time PCR technology can be employed for the screening of food samples for detecting the contaminating fungi.
机译:已经开发出一种高通量PCR阵列技术,用于通过使用实时PCR同时检测几种产霉菌毒素的真菌。根据涉及黄曲霉毒素,巴曲蛋白,单端孢菌素,伏马菌素和O曲霉毒素A的不同产生真菌毒素的生物合成途径的关键基因设计引物,并以统一的Tm(熔化温度)同时用于单个阵列中。这些引物以阵列形式排列,可在单个反应装置中同时检测14种产真菌毒素的真菌。使用从不同产真菌毒素的真菌分离的标准真实DNA验证了该方法,并使用SYBR Green 1荧光染料方法进行了实时PCR。经验证的方案用于通过使用从收集的食物样品中分离的DNA筛选市售食物样品。这些研究的结果表明,几种市售食品样品均被产真菌毒素的真菌污染。因此,这种高通量实时荧光定量PCR技术可用于筛选食品样品以检测污染真菌。

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