. Currents in biochemical research, 1956; twenty-seven essays charting the present course of biochemical research and considering the intimate relationship of biochemistry to medicine, physiology, and biology. Biochemistry -- Research. ^, \ cC-KETO GLUTARATE UREIDO group of purines, ^SUCCiNATSE formate, etc the al-corbon atom t rr. MNE I Glycine SUCCINATE- H GLYCINE HOOC-CH2-CH2-C-C-COOH CYCLE hOOC-CH2-CH2-C-CHo] 0 keto-glufaroldehyde II I 0 IMH2 cX-amino-p-kefo adipic acid(I) } CO â 2 \[0] HOOC-CH2-CH2-C-CH2NH2 0 - amino - levulinic ocid(ir) HOOC-CHo-CHp-C-COOH '⢠'-II 0 C<-ke?o-qlutoric
. Currents in biochemical research, 1956; twenty-seven essays charting the present course of biochemical research and considering the intimate relationship of biochemistry to medicine, physiology, and biology. Biochemistry -- Research. ^, \ cC-KETO GLUTARATE UREIDO group of purines, ^SUCCiNATSE formate, etc the al-corbon atom t rr. MNE I Glycine SUCCINATE- H GLYCINE HOOC-CH2-CH2-C-C-COOH CYCLE hOOC-CH2-CH2-C-CHo] 0 keto-glufaroldehyde II I 0 IMH2 cX-amino-p-kefo adipic acid(I) } CO â 2 \[0] HOOC-CH2-CH2-C-CH2NH2 0 - amino - levulinic ocid(ir) HOOC-CHo-CHp-C-COOH '⢠'-II 0 C<-ke?o-qlutoric acid I PORPHYRIN Fig. 1. Succinate-glycine cycle: a pathway for the metabolism of glycine (28,29). The problem of the biosynthesis of porphyrins, in the for- mation of the initial intermediates, can be considered, from a more general point of view, to be merely one aspect of the metab- olism of glycine. Many over-all aspects of glycine metabolism are now known, and especially the metabolic pattern of the a-carbon atom of glycine in its utilization for the synthesis of other compounds has been established. The a-carbon atom of 519. Please note that these images are extracted from scanned page images that may have been digitally enhanced for readability - coloration and appearance of these illustrations may not perfectly resemble the original Green, David Ezra, 1910-. New York, Interscience Publishers
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