J Biol Chem, Vol. 274, Issue 19, 13470-13479, May 7, 1999
A Novel Methyltransferase Catalyzes the Methyl Esterification
of trans-Aconitate in Escherichia coli
Hui
Cai and
Steven
Clarke
From the Department of Chemistry and Biochemistry and the Molecular
Biology Institute, University of California,
Los Angeles, California 90095-1569
We have identified a new type of
S-adenosyl-L-methionine-dependent
methyltransferase in the cytosol of Escherichia coli that is expressed in early stationary phase under the control of the RpoS
factor. This enzyme catalyzes the monomethyl esterification of
trans-aconitate at high affinity (Km = 0.32 mM) and cis-aconitate, isocitrate, and
citrate at lower velocities and affinities. We have purified the enzyme
to homogeneity by gel-filtration, anion-exchange, and hydrophobic
chromatography. The N-terminal amino acid sequence was found to match
that expected for the o252 open reading frame at 34.57 min
on the E. coli genomic sequence whose deduced amino acid
sequence contains the signature sequence motifs of the major class of
S-adenosyl-L-methionine-dependent methyltransferases. Overexpression of the o252 gene
resulted in an overexpression of the methyltransferase activity, and we
have now designated it tam for
trans-aconitate
methyltransferase. We have generated a knock-out strain of
E. coli lacking this activity, and we find that its growth
and stationary phase survival are similar to that of the parent strain.
We demonstrate the endogenous formation of trans-aconitate
methyl ester in extracts of wild type but not
tam
mutant cells indicating that
trans-aconitate is present in E. coli. Since
trans-aconitate does not appear to be a metabolic intermediate in these cells but forms spontaneously from the key citric
acid cycle intermediate cis-aconitate, we suggest that its
methylation may limit its potential interference in normal metabolic
pathways. We have detected trans-aconitate
methyltransferase activity in extracts of the yeast Saccharomyces
cerevisiae, whereas no activity has been found in extracts of
Caenorhabditis elegans or mouse brain.
Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.