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应用流式细胞技术快速定量检测UHT奶产品中的微生物 被引量:3

Quantitatively Detect Microorganism in UHT Milk Rapidly by Using Flow Cytometry
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摘要 采用基于单个活细胞的新型荧光标记技术,精确区分UHT奶样品中的活菌细胞与死细胞以及其他大颗粒物质,并应用流式细胞技术(flow cytometry,FCM)对UHT奶产品进行微生物快速定量检测。通过与传统的平板计数检测方法进行比对,结果表明,FCM方法的检测范围为10^1~10^7CFU/mL,远远高于平板计数法。2种方法的计数结果相关性分析表明,在一定菌液浓度范围内,FCM方法的定量结果与平板计数法线性相关良好,且对不同类型菌种都能精确标记定量,是更为快速、准确的检测方法。 In this research we distinguish the live cells, dead cells and other large particles accurately in the UHT milk samples using a new Fluorescence Labeling Technique basing on single live cell, and quickly detect micro- organism quantitatively by using flow cytometry. Comparison with traditional plate counting method shows that the detection range of FCM is 101 - 107 CFU/mL, far above that of plate counting method. Correlation analysis of the results of the two methods shows that within certain concentration range of bacteria solution, the results of FCM and plate counting method are linear, and FCM is a more accurate and rapid detection method for different types of microorganism.
出处 《食品与发酵工业》 CAS CSCD 北大核心 2011年第2期160-164,共5页 Food and Fermentation Industries
基金 国家质检总局科技计划项目(No.2009IK174)
关键词 流式细胞术 UHT奶 微生物 定量检测 flow cytometry, UHT milk, microorganism, quantitatively detect
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  • 1杨继忠,周祥山,解锡军,尤金花,张元兴,解福生.毕赤酵母发酵生产中的水蛭素降解顺序[J].微生物学通报,2004,31(5):24-27. 被引量:7
  • 2Porro D, Banzi B M, Smeraldi C. A double flow cytometric tag allows tracking of dynamics of cell cycle progression of newborn Saccharomyces cerevisiae cells during balanced exponential growth.Yeast, 1995,30:1157 ~ 1169.
  • 3Muller S, Hutter K J. Prozessoptimierung yon Reinzucht und Anstellverfaren mittels Flusscytometrle in sachssischen Brauereien.Monatsschr Brauqiss, 1999,3:40 ~ 48.
  • 4Krampera M, Tavecchia L, Benedetti F. Intracellular Cytokine profile of cord blood-T, and NK-cells and monocytes.Haematologica, 2000,85:675 ~ 679.
  • 5Patkar A,Vijayasankaran N,Urry D W,et al. Flow cytometry as a useful tool for process development: rapid evaluation of expression systems.J Biotechnol,2002,93(3) :217 ~ 229.
  • 6De Wulf P,Bmmbilla L,Vanoni M,et al.Real-time flow cytometric quantification of GFP expression and Gfp-fluorescence generation in Saccharomyces cerevisiae.J Microbiol Methods,2000,42( 1 ) :57 ~64.
  • 7Natarajan A, Subramanian S, Srienc F. Comparison of mutant forms of the green fluorescent protein as expression markers on Chinese hamster ovary (CHO) and Saccharomyces cerevisiae cells. J Biotechnol, 1998,62 : 29 ~ 45.
  • 8Zhao R, Natarajan A, Srienc F. A flow injection flow cytometry system for online monitoring of biorectors. Biotechnol Bioeng, 1999,62(5) :609 ~ 617.
  • 9Abu-Absi N R, Zamamiri A, Kacmar J, et al. Automated flow cytometry for acquisition of time-dependent population data.Cytometry ,2003,51A(2) :87 ~ 96.
  • 10Both B L, Poot M, Ylle S T. Baterial viability and antibiotic susceptibility test with SYTOX Green nucleic acid stain. Appl Environ Microbiol, 1997,3:2421 ~ 2431.

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