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Title: Mechanistic studies on the phytylation and methylation steps in bacteriochlorophyll a biosynthesis: an application of the /sup 18/O-induced isotope effect in /sup 13/C NMR

Journal Article · · Biochemistry; (United States)
OSTI ID:6522100

The high-resolution /sup 13/C NMR spectrum of bacteriochlorophyll a biosynthesized from (1-/sup 13/C,1,1,4-/sup 18/O/sub 3/)-5-aminolevulinic acid by growing cells of Rhodopseudomonas sphaeroides has shown both the C-17/sup 3/ and C-13/sup 3/ resonances consist of three additional components upfield shifted from the -/sup 16/O- /sup 13/C double bond /sup 16/O resonance. By comparison with the /sup 13/C NMR spectrum obtained for phytyl acetate containing /sup 13/C and /sup 18/O selectively in the ester linkage, these components have been identified as the bridge (-/sup 18/O- /sup 13/C double bond /sup 16/O), non bridge (-/sup 16/O-/sup 13/C double bond /sup 18/O), and dual-labeled (-/sup 18/O-/sup 13/C double bond /sup 18/O) isotopomers, These results have been interpreted to suggest that both the ester bonds of bacteriochlorophyll a are produced by a carboxy-alklyl transfer process.

Research Organization:
Univ. of Southampton, England
OSTI ID:
6522100
Journal Information:
Biochemistry; (United States), Vol. 26:4
Country of Publication:
United States
Language:
English