Direct counts of stained bacterial cells were compared with counts obtained from standard plating techniques. The method used by the authors combined acridine orange staining with 2‐(p‐iodophenyl)‐3‐(p‐nitrophenyl)‐5‐phenyl‐tetrazolium chloride reduction. To overcome the interference of a membrane filter's pores with the identification of stained cells, the authors used a gel‐stripping technique to transfer the bacterial cells from membrane filters to a gelatin matrix before counts were made. The method will supplement standard plate counts by determining metabolically active bacteria in a water sample within four hours.
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Diane S. Herson (1982) studied this question.
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