When Gomori's method for the histochemical demonstration of acid phosphatase (1941) was applied to various microorganisms, prominent staining of the polar bodies of corynebacteria was noticed. Gomori's method depends upon the action of the enzyme to separate the phosphate radical from the glycerophosphate in the incubation mixture, which in addition contains lead nitrate and acetate buffer, pH 5.0. The liberated phosphate combines with the lead at the site of the enzymatic activity. Subsequent treatment with ammonium sulfide converts the lead phosphate into dark, easily visible, lead sulfide. When the glycerophosphate was omitted from the incubation mixture, however, the same number of stained polar bodies w^ere observed. It was obvious, therefore, that this staining property did not depend on any specific enzymatic action. This observation led to a simple and efficient staining procedure for the identification of corynebacteria. STAINING TECHNIQUE (1) Fix and dry films in the usual manner by heat. (2) Either puit slides in a 10 per cent lead nitrate soluition at room temperatur'e for 15 minuites or longer, or cover slides with the lead nitrate solution, hold over flame, and heat gently for 2 to 3 minutes.