Abstract
A positive, genetic selection against the activity of the nitrogen regulatory (NTR) system was used to isolate insertion mutations affecting nitrogen regulation in Klebsiella aerogenes. Two classes of mutation were obtained: those affecting the NTR system itself and leading to the loss of almost all nitrogen regulation, and those affecting the nac locus and leading to a loss of nitrogen regulation of a family of nitrogen-regulated enzymes. The set of these nac-dependent enzymes included histidase, glutamate dehydrogenase, glutamate synthase, proline oxidase, and urease. The enzymes shown to be nac independent included glutamine synthetase, asparaginase, tryptophan permease, nitrate reductase, the product of the nifLA operon, and perhaps nitrite reductase. The expression of the nac gene was itself highly nitrogen regulated, and this regulation was mediated by the NTR system. The loss of nitrogen regulation was found in each of the four insertion mutants studied, showing that loss of nitrogen regulation resulted from the absence of nac function rather than from an altered form of the nac gene product. Thus we propose two classes of nitrogen-regulated operons: in class I, the NTR system directly activates expression of the operon; in class II, the NTR system activates nac expression and the product(s) of the nac locus activates expression of the operon.
MeSH Terms
Amino Acid Transport Systems
Asparaginase/metabolism
Escherichia coli Proteins
Gene Expression Regulation, Bacterial
Glutamate Dehydrogenase/metabolism
Glutamate-Ammonia Ligase/metabolism
Histidine Ammonia-Lyase/metabolism
Klebsiella pneumoniae/enzymology,genetics,metabolism
Membrane Transport Proteins/metabolism
Mutation
Nitrate Reductase
Nitrate Reductases/metabolism
Nitrogen/physiology
Operon
Saccharomyces cerevisiae Proteins
Sigma Factor/physiology
Urease/metabolism
beta-Galactosidase/metabolism
Chemicals
Amino Acid Transport Systems
Escherichia coli Proteins
Membrane Transport Proteins
Saccharomyces cerevisiae Proteins
Sigma Factor
TAT2 protein, S cerevisiae
TnaB protein, E coli
Glutamate Dehydrogenase
Nitrate Reductases
Nitrate Reductase
beta-Galactosidase
Asparaginase
Urease
Histidine Ammonia-Lyase
Glutamate-Ammonia Ligase
Nitrogen
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Macaluso A
Department of Biology, University of Michigan, Ann Arbor 48109.
Best E A
Bender R A
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