A simple and fast method for determining colony forming units

被引:159
作者
Sieuwerts, S. [1 ,2 ,3 ]
de Bok, F. A. M. [1 ,2 ]
Mols, E.
de Vos, W. M. [2 ,3 ]
Vlieg, J. E. T. van Hylckama [1 ,2 ]
机构
[1] Nizo Food Res, NL-6710 BA Ede, Netherlands
[2] Top Inst Food & Nutr, Wageningen, Netherlands
[3] Wageningen Univ, Microbiol Lab, Wageningen, Netherlands
关键词
colony forming units; Escherichia coli; faster enumeration; lactic acid bacteria; plating; Saccharomyces cerevisiae;
D O I
10.1111/j.1472-765X.2008.02417.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: To develop a flexible and fast colony forming unit quantification method that can be operated in a standard microbiology laboratory. Methods and Results: A miniaturized plating method is reported where droplets of bacterial cultures are spotted on agar plates. Subsequently, minicolony spots are imaged with a digital camera and quantified using a dedicated plug-in developed for the freeware program IMAGEJ. A comparison between conventional and minicolony plating of industrial micro-organisms including lactic acid bacteria, Eschericha coli and Saccharomyces cerevisiae showed that there was no significant difference in the results obtained with the methods. Conclusions: The presented method allows downscaling of plating by 100-fold, is flexible, easy-to-use and is more labour-efficient and cost-efficient than conventional plating methods. Significance and Impact of the Study: The method can be used for rapid assessment of viable counts of micro-organisms similar to conventional plating using standard laboratory equipment. It is faster and cheaper than conventional plating methods.
引用
收藏
页码:275 / 278
页数:4
相关论文
共 16 条
[1]   Development and evaluation of genome-probing microarrays for monitoring lactic acid bacteria [J].
Bae, JW ;
Rhee, SK ;
Park, JR ;
Chung, WH ;
Nam, YD ;
Lee, I ;
Kim, H ;
Park, YH .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (12) :8825-8835
[2]   Development of specific fluorescent oligonucleotide probes for in situ identification of wine lactic acid bacteria [J].
Blasco, L ;
Ferrer, S ;
Pardo, I .
FEMS MICROBIOLOGY LETTERS, 2003, 225 (01) :115-123
[3]   Automated counting of mammalian cell colonies by means of a flat bed scanner and image processing [J].
Dahle, J ;
Kakar, M ;
Steen, HB ;
Kaalhus, O .
CYTOMETRY PART A, 2004, 60A (02) :182-188
[4]  
GILCHRIS.JE, 1973, APPL MICROBIOL, V25, P244, DOI 10.1108/03068299810193425
[5]   Quantitative real-time PCR analysis of fecal Lactobacillus species in infants receiving a prebiotic infant formula [J].
Haarman, M ;
Knol, J .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2006, 72 (04) :2359-2365
[6]   Multichannel plating unit for high-throughput plating of cell cultures [J].
Hamilton, CM ;
Anderson, M ;
Lape, J ;
Creech, E ;
Woessner, J .
BIOTECHNIQUES, 2002, 33 (02) :420-423
[7]   Simplified agar plate method for quantifying viable bacteria [J].
Jett, BD ;
Hatter, KL ;
Huycke, MM ;
Gilmore, MS .
BIOTECHNIQUES, 1997, 23 (04) :648-650
[8]   Design and validation of 16S rRNA probes to enumerate members of the Clostridium leptum subgroup in human faecal microbiota [J].
Lay, C ;
Sutren, M ;
Rochet, V ;
Saunier, K ;
Doré, J ;
Rigottier-Gois, L .
ENVIRONMENTAL MICROBIOLOGY, 2005, 7 (07) :933-946
[9]  
Liu Bailing, 2004, Am J Pharmacogenomics, V4, P263, DOI 10.2165/00129785-200404040-00006
[10]   High-throughput imaging of bacterial colonies grown on filter plates with application to serum bactericidal assays [J].
Liu, X ;
Wang, S ;
Sendi, L ;
Caulfield, MJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 2004, 292 (1-2) :187-193