Chemical and Pharmaceutical Bulletin p. 1311 - 1317 (1995)
Update date:2022-08-29
Topics:
Okazaki
Kajiwara
The biosynthetic pathway of bacteriochlorophyll-a in Rhodopseudomonas spheroides was investigated by administration of [2-13C]glycine, L-[methyl- 13C]methionine, L-[1-13C]glutamic acid and 13C- or 15N-labeled δ- aminolevulinic acid (ALA). The origin of the hydrogen atoms was studied by following the incorporation into bacteriochlorophyll of 13C-labeled ALA in a medium containing 50% D2O and that of 2H-, 13C-labeled ALA. The labeled bacteriochlorophylls were converted into more stable methyl bacteriopheophorbides, which were subjected to 13C-NMR analyses to obtain information about the biosynthetic origin of the hydrogen atoms. The use of 13C-enriched bacteriochlorophylls and methyl bacteriopheophorbides allowed us to make 13C-NMR signal assignments for all carbons of the porphyrin nucleus.
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