SummaryStandardized and reliable methods have been devised to assay preparations of the glutamic oxaloacetic transaminase from human erythrocytes by the CAS principle, i.e., the unsaturation and saturation of the coenzyme (pyridoxal 5'-phosphate) of a Coenzyme-Apoenzyme System. This dual enzymic assay is effective to detect and measure human deficiencies of vitamin B6. A preferred procedure has been developed, particularly for individuals and for limited groups, but is also applicable to large groups. A simplified procedure, which emphasizes the statistical significance of difference between large groups was also developed. Lyophilized erythrocyte hemolysates appear stable for up to 7 days for simplified transportation. KISHI et al. (1) recently reviewed the background of this research in connec tion with their first study of the parameters of the assay of the glutamic oxaloacetic transaminase by the CAS principle. This background need not be fully repeated herein. Suffice it to say that the report by BRIM et al. (2) in 1960 on the effect of a thiamine deficiency on the enzyme activity of a transketolase in erythrocyte hemolysates opened an enzymic methodology to determine a vitamin deficiency which was based upon the activity of an enzyme requiring the vitamin or its co enzyme form. Previous methodologies to determine vitamin deficiencies had been based upon determinations of the vitamin as a chemical substance, and the determinations were usually organic chemical, or were based upon a physical prop erty, or were by a microbiological procedure. This newer enzymic methodology for the detection and measurement of a vitamin deficiency is based upon a principle, defined by FOLKERS (3), as follows: "The specific activity of a coenzyme-apoenzyme 1 Human Deficiencies of Vitamin B6 . II.
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