skip to main  |
      skip to sidebar
        
      
        
      
                   
Abstract: We have developed a three-component system  for microbial identification that consists of (i) a universal  syringe-operated                      silica minicolumn for successive DNA and RNA  isolation, fractionation, fragmentation, fluorescent labeling, and  removal of                      excess free label and short oligonucleotides; (ii)  microarrays of immobilized oligonucleotide probes for 16S rRNA  identification;                      and (iii) a portable battery-powered device for  imaging the hybridization of fluorescently labeled RNA fragments with  the                      arrays. The minicolumn combines a guanidine  thiocyanate method of nucleic acid isolation with a newly developed  hydroxyl radical-based                      technique for DNA and RNA labeling and  fragmentation. DNA and RNA can also be fractionated through differential  binding of                      double- and single-stranded forms of nucleic acids  to the silica. The procedure involves sequential washing of the column                      with different solutions. No vacuum filtration  steps, phenol extraction, or centrifugation is required. After  hybridization,                      the overall fluorescence pattern is captured as a  digital image or as a Polaroid photo. This three-component system was  used                      to discriminateEscherichia coli, Bacillus subtilis, Bacillus thuringiensis,  and human HL60 cells. The procedure is rapid: beginning with whole  cells, it takes approximately 25 min to obtain labeled                      DNA and RNA samples and an additional 25 min to  hybridize and acquire the microarray image using a stationary image  analysis                      system or the portable imager. 
 
 
 
        
    
 
  
 
 
 
0 comments:
Post a Comment