Abstract
For the application of glycerol dehydrogenase from a strain of bacterial Erwinia aroideae, a method of measuring serum aldolase activity is determined. This method is possible to measure 0-50 mU/ml aldolase. Until now, spectrophotometric assay with glycerol-1-phosphate dehydrogenase and colorimetric determination with 2, 4-dinitrophenylhydrazine are available. The former is possible to be affected with serum alkaline phosphatase, the latter needs much serum. Correlation between spectrophotometric assay with glycerol-1-phosphate dehydrogenase and this method using rabbit serum experimentally increased aldolase activity is shown.
