transketolase; 1 j,M U-'4C-fructose-6-P, specific radioactivity 0.4 mcj,'mmole; 20 ,ig of chlorophyll in a total volume of 0.33 ml.The assay was performed at 20 C in a controlled temperature bath equipped with incandescent lighting of 1200 ft-c. The reaction was stopped by adding 0.34 ml of boiling absolute ethyl alcohol, and the tubes were removed to an 80 C water bath for 3 min. The test tubes were then centrifuged at 10,000g for 10 min, and the glycolate present in the supernatant fraction was determined. The supernatant fluid was applied to a Dowex AG 1X8 acetate (100-200 mesh) column (6 X 50 cm), and glycolate was eluted according to the method of Zelitch (33). After application of the sample the column was washed with 15 ml of H20. Glycolate was eluted with 10 ml of 4 M acetic acid. Paper chromatography in a 1-butanol, propionic acid, water solvent (9.4:3:4 v, 'v) confirmed that the eluate contained only glycolate. In this procedure more than 99.9%O of the U-14C-fructose-6-P applied was retained in the column. The recovery of added glycolate-U-14C was better than 95%c A 3-ml aliquot of the acetic acid eluate was placed in 15 ml of a liquid scintillation mixture consisting of 100 g of naphthalene,