Affiliation:
1. Department of Biology, The University of Michigan, Ann Arbor, Michigan 48109-1048
Abstract
ABSTRACT
The nitrogen assimilation control gene,
nac
, was detected in
Escherichia coli
but not in
Salmonella typhimurium
by Southern blotting, using a probe from the
Klebsiella aerogenes nac
(
nac
K
) gene. The
E. coli nac
gene (
nac
E
) was isolated from a cosmid clone by complementation of a
nac
mutation in
K. aerogenes. nac
E
was fully functional in this complementation assay. DNA sequence analysis showed considerable divergence between
nac
E
and
nac
K
, with a predicted amino acid sequence identity of only 79% and most of the divergence in the C-terminal half of the protein sequence. The total predicted size of NAC
E
is 305 amino acids, the same as for NAC
K
. A null mutation,
nac-28
, was generated by reverse genetics. Mutants bearing
nac-28
have a variety of phenotypes related to nitrogen metabolism, including slower growth on cytosine, faster growth on arginine, and suppression of the failure of an Ntr-constitutive mutant to grow with serine as sole nitrogen source. In addition to a loss of nitrogen regulation of histidase formation,
nac-28
mutants also showed a loss of a weak repression of glutamate dehydrogenase formation. This repression was unexpected because it is balanced by a NAC-independent activation of glutamate dehydrogenase formation during nitrogen-limited growth. Attempts to purify NAC
E
by using methods established for NAC
K
failed, and NAC
E
appears to be degraded with a half-life at 30°C as short as 15 min during inhibition of protein synthesis.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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4
9
American Society for Microbiology
Washington D.C
Cited by
62 articles.
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