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[一种用于检测食品中大肠杆菌O157:H7的快速分离培养方法的建立]

[Development of a rapid separating incubation method for detection of Escherichia coli O157:H7 in food].

作者信息

Wang Jing, Qiu Maofeng, Lin Xiuguang

机构信息

China Import & Export Commodity Inspect Technology Institute, Beijing 100025, China.

出版信息

Wei Sheng Yan Jiu. 2002 Feb;31(1):44-6.

Abstract

To detect Escherichia coli O157:H7 in food, a selective and differential medium, CTV-MUG-RSMAC agar, was designed. Using this medium, the growth of most interfering organisms could be inhibited, and three main biochemical characteristics, including sorbitol-negative, rahmnose-negative and MUG-negative, to identify E. coli O157:H7 could also be simultaneously recognized. Sorbitol-positive aberrance strains of E. coli O157:H7 could be distinguished on the medium. The procedure of detecting food sample includes adding sample to selective broth and incubating overnight at 42 degrees C, streaking the inoculum to CTV-MUG-RSMAC agar and incubating at 37 degrees C for 24 h, and picking the typical colonies to react with sera for O157 and H7 antigens, and then take biochemical tests. The procedure could be finished within 3 days. This method has been applied to 126 food samples, and E. coli O157:H7 was detected from 3 samples. The results were in coincidence with those using FDA method.

摘要

为检测食品中的大肠杆菌O157:H7,设计了一种选择性鉴别培养基——CTV-MUG-RSMAC琼脂。使用该培养基,可抑制大多数干扰菌的生长,同时还能识别用于鉴定大肠杆菌O157:H7的三个主要生化特性,即山梨醇阴性、鼠李糖阴性和MUG阴性。在该培养基上可区分大肠杆菌O157:H7的山梨醇阳性变异菌株。食品样品检测程序包括将样品加入选择性肉汤中,于42℃过夜培养,将接种物划线接种于CTV-MUG-RSMAC琼脂上,于37℃培养24小时,挑取典型菌落与O157和H7抗原血清反应,然后进行生化试验。该程序可在3天内完成。该方法已应用于126份食品样品,从3份样品中检测到大肠杆菌O157:H7。结果与使用FDA方法的结果一致。

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