Abstract
L-[1-14 C]lysine was prepared using a technique based on the differential solubility of the diastereomeric salts of DL-lysine with L-glutamic acid. D-[l-14 C]llysine was prepared by the enzymatic removal of residual L-[l-14 cl]ysine from the reaction mixture remaining after the preparation of L-[1-141- C]lysine. The products were tested with L-lysine decarboxylase and by column chromatography. L-[l-14C]lysine was obtained in 60% yield with a steroisomeric purity of 95.1%, and D-[l-14 cllysine was obtained in a slightly higher yield with a steroisomeric purity of 97.5%.