Abstract
DNA was prepared from a strain of Escherichia coli bearing a mutation which confers the GlnC phenotype (inability to reduce the expression of glnA and other nitrogen-regulated operons in response to ammonia in the growth medium). A fragment of this DNA carrying glnA, the structural gene for glutamine synthetase, was cloned on plasmid pBR322. By using recombination in vitro, we mapped the GlnC mutation to a region between glnA and glnG. This region defines a gene, glnL, which codes for a trans-acting product; the GlnC mutant produces an altered product. The glnL product plays a key role in the communication of information concerning the quality and abundance of the nitrogen source in the growth medium to a destination responsible for the regulation of glnA and other genes for enzymes responsible for nitrogen utilization.
MeSH Terms
Ammonia/pharmacology
Cloning, Molecular
Escherichia coli/genetics,metabolism
Genes, Bacterial
Genes, Regulator
Glutamate-Ammonia Ligase/genetics
Histidine Ammonia-Lyase/metabolism
Mutation
Nitrogen/metabolism
Operon
Chemicals
Ammonia
Histidine Ammonia-Lyase
Glutamate-Ammonia Ligase
Nitrogen
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Chen Y M
Backman K
Magasanik B
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26 references, click to expand
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