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特异性检测植物乳杆菌的多重PCR方法
引用本文:陈臣,周方方,任婧,刘振民,陈卫. 特异性检测植物乳杆菌的多重PCR方法[J]. 广西农业科学, 2013, 0(7): 1076-1080
作者姓名:陈臣  周方方  任婧  刘振民  陈卫
作者单位:[1]江南大学食品学院/食品科学与技术国家重点实验室,江苏无锡214122 [2]光明乳业股份有限公司研究阮,乳业生物技术国家重点实验室,上海200436
基金项目:“十二五”国家863计划项目(2011AA100901)
摘    要:【目的】建立特异性检测植物乳杆菌的方法,排除近缘菌的干扰。【方法】利用SMM系统筛选植物乳杆菌种特异序列,根据特异序列设计引物进行不同乳制品的多重PCR检测。【结果】设计的7对引物具有良好的种特异性,其中3对引物可以排除戊糖乳杆菌和副植物乳杆菌的干扰,可扩增获得植物乳杆菌的特异条带101bp(引物LP-1和LP-2)、189bp(引物LP-5和LP-6)、378bp(引物LP-9和LP-10)。该方法的检测限为2.2×10CFU/mL。采用多重PCR检测与琼脂糖凝胶电泳图谱分析对自制含有各种乳酸菌酸奶产品、自然发酵产品及市售酸乳产品中植物乳杆菌进行定性检测,可以特异性检测出植物乳杆菌,准确区分植物乳杆菌的近缘菌株。【结论】该多重PCR方法成本低、步骤简单、耗时短、灵敏度高,具有特异性,可作为快速检测植物乳杆菌种的方法在生产中使用。

关 键 词:植物乳杆菌  SMM系统  多重PCR  定性检测

A specific method for detection of Lactobacillus plantarum by multiplex PCR
CHEN Chen,ZHOU Fang-fang,REN Jing,LIU Zhen-min,CHEN Wei. A specific method for detection of Lactobacillus plantarum by multiplex PCR[J]. Guangxi Agricultural Sciences, 2013, 0(7): 1076-1080
Authors:CHEN Chen  ZHOU Fang-fang  REN Jing  LIU Zhen-min  CHEN Wei
Affiliation:1 (1School of Food Science and Technology/State Key Laboratory of Food Science & Technology, Jiangnan University, Wuxi, Jiangsu 214122, China; 2Bright Dairy Research Institute of Bright Dai2 Co., Ltd., /State Key Laboratory of Dairy Industry Biotechnology, Shanghai 200436, China)
Abstract:[Objective]The present study was conducted to establish a specific method for detection of Lactobacillus plantarum without any interference. [Method ]Laetobacillus plantamm specific sequenees were screened by SMM system, and muhiplex PCR detection of different dairy products was conducted based on the designed primer of specific sequences. [Result]The designed seven primers performed good specificity, among which three primers, fi'ee from the interference of Lactobaeillus pentosus and LactobacilIus plantamm, could produce specific sequences of 101 bp (Primer LP-1 & LP-2), 189 bp (Primer LP-5 & LP-6) and 378 bp (Primer LP-9 & LP-10). The limit of detection was 2.2x10 CFU/mL . Using multiplex PCR and agarose gel electrophoresis to test self-made yogurt products with lactic acid bacteria, natural ferment- ed products, and yogurts commodities, Laetobacillus plantarum could be detected to distinguish kindred strains of Lacto- bacillus plantarum. [Conclusion]Due to its low cost, simple procedures, brief time, high sensitivity and specificity, this method should be used for fast detection of Lactobacillus plantarum in actual production.
Keywords:Lactobacillus plantarum  SMM system  multiplex PCR  qualitative detection
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