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Differentiation of Clostridium perfringens and Clostridium botulinum fromnon-toxigenic clostridia, isolated from prepared and frozen foods byPCR-DAN based methods

机译:基于PCR-DAN的方法从制备和冷冻食品中分离出产气荚膜梭菌和肉毒梭菌与非产毒梭菌的区别

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摘要

During the elaboration process of prepared and frozen foods, Clostridium sp. have been reported. From those microorganisms, C. perfringens and C. botulinum may pose a high risk for the consumers. To avoid these pathogenic organisms an HACCP program should be implemented, but in addition sensitive and moderately time consuming microbiological methods for monitoring C. perfringens and C. boulinum should be established. In this work, an RFLP analysis of the 16S rDNA will be developed to differentiate C. perfringens from other Clostridium sp. In addition, a PCR protocol, will be assayed to detect C. botulinum. Both two methods will be compared with biochemical characterization by API system. The restriction analysis of the 16S rDNA with Tag I and Rsa I showed at least the same sensitivity to differentiate C. perfringens from clostridial isolates as biochemical identification. However, the former method takes only 8-10 h of analysis as compared with 24-48 h required for biochemical characterization. With the specific PCR protocol to detect C. botulinum a band of 1.1 kbp was obtained derived from the specific amplification of BoNT genes, taking 6-8 h for analysis. Both two molecular DNA based methods should be considered as verification techniques of pathogenic clostridia in the HACCP program.
机译:在制备和冷冻食品的过程中,梭状芽孢杆菌已经汇报过。从这些微生物中,产气荚膜梭菌和肉毒梭菌可能对消费者构成高风险。为避免这些致病性生物,应实施HACCP程序,但除此之外,还应建立灵敏且耗时的微生物方法来监测产气荚膜梭菌和布氏梭菌。在这项工作中,将对16S rDNA进行RFLP分析,以区分产气荚膜梭菌和其他梭状芽胞杆菌。另外,将分析PCR方案以检测肉毒梭菌。两种方法都将通过API系统与生化特性进行比较。对具有标签I和Rsa I的16S rDNA进行的限制性酶切分析显示,至少有相同的敏感性可以将生气荚膜梭菌从梭菌中分离出来,作为生化鉴定。但是,前一种方法仅需8-10小时的分析,而生化特性分析则需要24-48小时。使用特异性PCR方案检测肉毒梭菌,从BoNT基因的特异性扩增获得了1.1 kbp的条带,需要6-8小时进行分析。在HACCP程序中,两种基于分子DNA的方法都应被视为致病性梭菌的验证技术。

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