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Volume 270,
Number 2,
Issue of January 13, 1995 pp. 638-646
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
Utilization
of Aspartate as a Nitrogen Source in Escherichia coli ANALYSIS OF NITROGEN FLOW AND CHARACTERIZATION OF THE PRODUCTS
OF ASPARTATE CATABOLISM
(Received for publication, July 20,
1994; and in revised form, October 14, 1994)
Warren J.
Goux ,
Anita A. D.
Strong,
Barbara
L.
Schneider,
W.-N. Paul
Lee ,
Lawrence J.
Reitzer
N NMR, reverse-phase high performance liquid
chromatography and gas chromatography/mass spectrometry have been used
to follow nitrogen metabolism in Escherichia coli labeled on
medium containing L-[ N]aspartate. The
flow of N through various nitrogen-containing metabolites
was followed over the course of the labeling period. For wild-type E. coli labeled on L-[ N]aspartate as sole source of
nitrogen, significant N labeling was detected only in the
intracellular L-glutamate, L-alanine, L-aspartate, and putrescine pools. Intracellular
concentrations of L-aspartate and L-glutamate
differed significantly in extracts of an arginine auxotroph (argG ), which is deficient in a potential
aspartate-assimilating reaction. When the L-[ N]aspartate containing labeling
medium was supplemented with unlabeled arginine, extracts of wild-type E. coli were shown to contain significant amounts of unlabeled
ammonia and putrescine. There was substantial dilution of N in the glutamate pool. The observation that glutamate,
aspartate, and alanine are N-labeled, but ammonia is not,
suggests that these amino acids are not the immediate source of
ammonia. Our results suggest that arginine may be an intermediate for
the degradation of some of the aspartate and that arginine may be an
intermediate for ammonia production during nitrogen-limited growth. Our
results also strongly suggest the presence of a previously
uncharacterized pathway of arginine degradation.

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Copyright © 1995 by the American Society for Biochemistry and Molecular Biology.
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