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J. Bacteriol., Oct 1995, 5778-5783, Vol 177, No. 20
DW Bollivar, T Elliott and SI Beale
It was recently reported (H. Akutsu, J.-S. Park, and S. Sano, J. Am. Chem.
Soc. 115:12185-12186, 1993) that in the strict anaerobe Desulfovibrio
vulgaris methyl groups from exogenous L-methionine are incorporated
specifically into the 1 and 3 positions (Fischer numbering system) on the
heme groups of cytochrome c3. It was suggested that under anaerobic
conditions, protoporphyrin IX biosynthesis proceeds via a novel pathway
that does not involve coproporphyrinogen III as a precursor but instead may
use precorrin-2 (1,3-dimethyluroporphyrinogen III), a siroheme and vitamin
B12 precursor which is known to be derived from uroporphyrinogen III via
methyl transfer from S-adenosyl-L- methionine. We have critically tested
this hypothesis by examining the production of protoporphyrin IX-based
tetrapyrroles in the presence of exogenous [14C]methyl-L-methionine under
anaerobic conditions in a strict anaerobe (Chlorobium vibrioforme) and a
facultative anaerobe (Rhodobacter capsulatus). In both organisms, 14C was
incorporated into the bacteriochlorophyll precursor, Mg-protoporphyrin IX
monomethyl ester. However, most of the label was lost upon base hydrolysis
of this compound to yield Mg-protoporphyrin IX. These results indicate that
although the administered [14C]methyl-L-methionine was taken up, converted
into S-adenosyl-L-methionine, and used for methyl transfer reactions,
including methylation of the 6-propionate of Mg- protoporphyrin IX, methyl
groups were not transferred to the porphyrin nucleus of Mg-protoporphyrin
IX.(ABSTRACT TRUNCATED AT 250 WORDS)
Copyright © 1995, American Society for Microbiology
Anaerobic protoporphyrin biosynthesis does not require incorporation of methyl groups from methionine
Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912, USA.
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