Technique DNASE
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Principle DNAse can be used as differential test for strains of Staphylococci
Cautions  
Method DNA plates contain polymeric DNA which can be hydrolysed to nucleic acids by the DNAse. After 24 hours incubation at 37 degrees C, the inoculated plate is flooded with 1 N hydrochloric acid, which will precipitate undigested DNA but will leave a clear zone around the DNAse positive strains. Alternatively, the plate may be flooded with 0.1% toluidine blue. A pink colour is produced around the growth of DNAse producers. The test is useful for the study of Bacillus, Staphylococcus, Streptococcus and Pseudomonas.
Results  
Positive control  
Negative control  
Reagents  
Reference