华南理工大学学报(自然科学版) ›› 2010, Vol. 38 ›› Issue (9): 142-146.doi: 10.3969/j.issn.1000-565X.2010.09.027

• 生物工程 • 上一篇    下一篇

PMA与PCR结合的细菌活细胞检测方法

罗剑飞 林炜铁 郭勇   

  1. 华南理工大学 生物科学与工程学院, 广东 广州 510006
  • 收稿日期:2009-10-09 修回日期:2009-12-25 出版日期:2010-09-25 发布日期:2010-09-25
  • 通信作者: 罗剑飞(1984-),男,博士生,主要从事环境微生物理论与应用研究. E-mail:ljfjt2002@163.com
  • 作者简介:罗剑飞(1984-),男,博士生,主要从事环境微生物理论与应用研究.
  • 基金资助:

    广东省农业科技攻关项目(2008B021000036)

Detection of Viable Bacterium Cells Based on Propidium Monoazide in Combination with PCR

Luo Jian-fei  Lin Wei-tie  Guo Yong   

  1. School of Biological Science and Engineering,South China University of Technology,Guangzhou 510006,Guangdong,China
  • Received:2009-10-09 Revised:2009-12-25 Online:2010-09-25 Published:2010-09-25
  • Contact: 罗剑飞(1984-),男,博士生,主要从事环境微生物理论与应用研究. E-mail:ljfjt2002@163.com
  • About author:罗剑飞(1984-),男,博士生,主要从事环境微生物理论与应用研究.
  • Supported by:

    广东省农业科技攻关项目(2008B021000036)

摘要: 基于PCR的分子生物技术在检测过程中不能有效区分样品中细菌的死活状态,这会导致对细菌数量的错误估计.文中用叠氮溴化丙锭(PMA)对样品基因组提取进行前处理,使PMA与样品中死细胞的DNA分子共价交联,并抑制该DNA分子的PCR扩增.结果表明:当样品中PMA质量浓度大于3μg/mL、曝光时间大于3 min时,PMA可抑制细胞膜破裂的E.coli死细胞DNA的PCR扩增;PMA质量浓度高于50μg/mL时对活细胞DNA的PCR扩增有一定影响;当浊度小于10NTU时,PMA能有效地抑制死细胞DNA的PCR扩增,而当浊度大于100NTU时,PMA失去效果.

关键词: 叠氮溴化丙锭, 脱氧核糖核酸, 聚合酶链反应, 活细胞检测

Abstract:

PCR-based molecular biotechnologies are ineffective in discriminating dead cells from viable ones,which may result in inaccurate estimation of cell number.In order to solve this problem,propidium monoazide(PMA) treatment was used as a pretreatment for the genome extraction of environmental samples,in which PMA covalently crosslinks with DNA molecules in dead cells and inhibits the PCR amplification of DNA molecules.The results indicate that the PCR amplification of DNA from heat-killed E.coli cells can be inhibited by PMA with a mass concentration of 3μg/mL after an exposure for more than 3min,while the PCR amplification of DNA from viable cells is slightly inhibited by PMA with a mass concentration of more than 50μg/mL,and that PMA treatment is effective when the turbidity is less than 10 NTU and is ineffective when the turbidity is greater than 100NTU.

Key words: propidium monoazide, deoxyribonucleic acid, polymerase chain reaction, viable cell detection