Different samples representing biotechnology, agriculture, medicine, food microbiology, environmental microbiology and applied microbiology where there was no clear idea about the prevalent bacterial or yeast cfu in the sample were tested through the SP-SDS approach. The preferred dilutions from the anchored stocks included 100–105 or 101–106 for liquid samples, and 101–106 for solid samples avoiding the particulate 100. Further, SP-SDS was tried for parallel testing of two or multiple samples in a plate. This included testing the effect due to different diluents on E. cloacae where the 100 stock in FDW was taken through serial dilution in saline (NaCl 9 g l−1), phosphate buffered saline (PBS), peptone–water (10 g l−1 peptone and 5 g l−1 NaCl; pH 7.2) [1] , peptone-salt (1 g l−1 each peptone and NaCl; pH 7.0; [23] (link)) or nutrient broth (pH 7.4) employing FDW as control. In another trial, E. cloacae dilutions prepared in FDW and peptone salt was monitored with SP–SDS after static incubation over 5 h at 20 min intervals during the initial one hour and hourly thereafter employing the decimal dilutions 103–108. Further experimental details are provided under Results and Discussion.
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