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J. Bacteriol., Nov 1997, 6921-6928, Vol 179, No. 22
KE de Rudder, JE Thomas-Oates and O Geiger
Phosphatidylcholine (PC) is the major membrane-forming phospholipid in
eukaryotes. In addition to this structural function, PC is thought to play
a major role in lipid turnover and signalling in eukaryotic systems. In
prokaryotes, only some groups of bacteria, among them the members of the
family Rhizobiaceae, contain PC. To understand the role of PC in bacteria,
we have studied Rhizobium meliloti 1021, which is able to form
nitrogen-fixing nodules on its legume host plants and therefore has a very
complex phenotype. R. meliloti was mutagenized with
N-methyl-N'-nitro-N-nitrosoguanidine, and potential mutants defective in
phospholipid N-methyltransferase were screened by using a colony
autoradiography procedure. Filters carrying lysed replicas of mutagenized
colonies were incubated with S-adenosyl-L-[methyl- 14C]methionine.
Enzymatic transfer of methyl groups to phosphatidylethanolamine (PE) leads
to the formation of PC and therefore to the incorporation of radiolabel
into lipid material. Screening of 24,000 colonies for reduced incorporation
of radiolabel into lipids led to the identification of seven mutants which
have a much-reduced specific activity of phospholipid N-methyltransferase.
In vivo labelling of mutant lipids with [14C]acetate showed that the
methylated PC biosynthesis intermediates phosphatidylmonomethylethanolamine
and phosphatidyldimethylethanolamine are no longer detectable. This loss is
combined with a corresponding increase in the potential methyl acceptor PE.
These results indicate that PC biosynthesis via the methylation pathway is
indeed blocked in the mutants isolated. However, mass spectrometric
analysis of the lipids shows that PC was still present when the mutants had
been grown on complex medium and that it was present in the mutants in
wild-type amounts. In vivo labelling with [methyl-14C]methionine shows that
in phospholipid N-methyltransferase-deficient mutants, the choline moiety
of PC is not formed by methylation. These findings suggest the existence of
a second pathway for PC biosynthesis in Rhizobium.
Copyright © 1997, American Society for Microbiology
Rhizobium meliloti mutants deficient in phospholipid N- methyltransferase still contain phosphatidylcholine
Institute of Biotechnology, Technical University of Berlin, Germany.
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