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多重PCR技术检测微生物肥料中巨大芽孢杆菌和蜡样群芽孢杆菌的研究与应用
引用本文:曹凤明,李 俊,沈德龙,关大伟,李 力.多重PCR技术检测微生物肥料中巨大芽孢杆菌和蜡样群芽孢杆菌的研究与应用[J].微生物学通报,2009,36(9):1436-1441.
作者姓名:曹凤明  李 俊  沈德龙  关大伟  李 力
作者单位:1. 中国农业科学院农业资源与农业区划研究所,北京,100081;农业部微生物肥料和食用菌菌种质量监督检验测试中心,北京,100081
2. 农业部微生物肥料和食用菌菌种质量监督检验测试中心,北京,100081
3. 中国农业科学院农业资源与农业区划研究所,北京,100081
基金项目:中国农科院农业资源与农业区划研究所中央级公益性科研院所基本科研业务费专项资金资助(No. 2009-11)
摘    要:巨大芽孢杆菌是微生物肥料生产中的常用菌种, 与之形态上相似的蜡样群芽孢杆菌(蜡样芽孢杆菌、苏云金芽孢杆菌、蕈状芽孢杆菌)则是产品中常见的污染菌, 传统方法区分两者费时费力, 有必要建立检测这两类芽孢杆菌的PCR方法。本文利用已登录的spoOA基因序列分别设计和筛选了上述两个种(群)的特异引物, 并建立了多重PCR检测技术。使用该方法对巨大芽孢杆菌、蜡样群芽孢杆菌和其他芽孢菌共3属13种24株标准菌株的基因组DNA进行扩增, 以检验其特异性。结果显示, 巨大芽孢杆菌、蜡样群芽孢杆菌基因组DNA分别产生大小不同的唯一产物, 其他芽孢杆菌均为阴性。该多重PCR检测方法的灵敏度经测定为105 CFU/mL。同时对10株待测菌株和8个微生物肥料产品进行检测, 其鉴定结果与常规鉴定结果一致。以上结果表明, 本文建立的多重PCR方法具有较高的特异性和灵敏度, 可快速、准确鉴定巨大芽孢杆菌和蜡样群芽孢杆菌, 在微生物肥料检测方面有良好的实用前景。

关 键 词:巨大芽孢杆菌    蜡样群芽孢杆菌    多重PCR    种(群)特异引物    检测

Multiplex-PCR Approach to Identify Bacillus megaterium and Bacillus cereus Group Applied in Microbial Fertilizers
CAO Feng-Ming,LI Jun,SHEN De-Long,GUAN Da-Wei and LI Li.Multiplex-PCR Approach to Identify Bacillus megaterium and Bacillus cereus Group Applied in Microbial Fertilizers[J].Microbiology,2009,36(9):1436-1441.
Authors:CAO Feng-Ming  LI Jun  SHEN De-Long  GUAN Da-Wei and LI Li
Institution:Institute of Agricultural Resources and Regional Planning, Chinese Academy of Agricultural Sciences, Beijing 100081, China; Center for Quality Supervision and Test of Microbial Fertilizers and Mushroom Spawn, Ministry of Agriculture, Beijing 100081, China;Center for Quality Supervision and Test of Microbial Fertilizers and Mushroom Spawn, Ministry of Agriculture, Beijing 100081, China;Institute of Agricultural Resources and Regional Planning, Chinese Academy of Agricultural Sciences, Beijing 100081, China;;Center for Quality Supervision and Test of Microbial Fertilizers and Mushroom Spawn, Ministry of Agriculture, Beijing 100081, China;Center for Quality Supervision and Test of Microbial Fertilizers and Mushroom Spawn, Ministry of Agriculture, Beijing 100081, China
Abstract:Bacillus megaterium strains are commonly used in microbial fertilizer (MF). MF products are often contaminated by other B. cereus group members, which have similar phenotype such as Bacillus cereus, B. thuringiensis, B. mycoide. For quality control and safety of MF, a rapid and accurate method is needed to distinguish the strains of Bacillus megaterium from B. cereus group. Based on specific nucleotide sequences of the spoOA genes, 2 pairs of species-specific primers were designed and a multiplex-PCR (mPCR) was developed for this purpose. When the optimized mPCR was used to detect the DNAs of 24 reference strains from three genera of Bacillus, Paenibacillus, and Brevibacillus, all B. megaterium strains showed single fragment of 443 bp and Bacillus cereus group showed a fragment of 411 bp. However, no any amplified product was from the other bacteria. The sensitivity of mPCR was 105 CFU/mL. The mPCR results of 10 isolates of B. megaterium/B. cereus group and 8 products of MF coincided with the biochemical assay. Taken together, our newly developed mPCR assay was species-specific and effective in application. It can be used to detect and identify the strains of B. megaterium and B. cereus group from microbial fertilizer products.
Keywords:Bacillus megaterium  Bacillus cereus group  Multiplex-PCR  Species-specific primers  Detection
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