Rapid fluorometric quantification of bacterial cells using Redsafe nucleic acid stain
Background and Objectives: Numerous procedures in biology and medicine require the counting of cells. Direct enumer- ation of Colony Forming Units (CFUs) is time-consuming and dreary accurate cell counting on plates with high numbers of CFUs is error prone. In this study we report a new indirect ce...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Tehran University of Medical Sciences
2016-02-01
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Series: | Iranian Journal of Microbiology |
Subjects: | |
Online Access: | https://ijm.tums.ac.ir/index.php/ijm/article/view/808 |
Summary: | Background and Objectives: Numerous procedures in biology and medicine require the counting of cells. Direct enumer- ation of Colony Forming Units (CFUs) is time-consuming and dreary accurate cell counting on plates with high numbers of CFUs is error prone. In this study we report a new indirect cell counting method that was developed based on the use of Redsafe fluorometric assay. The usefulness of Redsafe, a nucleic acid stain, in liquid medium is based on the binding of the fluorescent dye to DNA.
Materials and Methods: Redsafe fluorometric assay was evaluated in comparison with MTT colorimetric assay as a colou- rimetric assay for enumeration of bacterial cells.
Results: Obtained results showed that fluorometric assay threshold for LB grown E. coli is 6×104 CFU/ml. Redsafe fluo- rescent assay can be used as a rapid and inexpensive method for bacterial enumeration and quantification with increased sensitivity.
Conclusion: The sensitivity of the Redsafe fluorometric assay for detection and enumeration of bacterial cells was 2-log-unit more than that was observed for the MTT assay.
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ISSN: | 2008-3289 2008-4447 |