| Literature DB >> 6120930 |
Y M Chen, K Backman, B Magasanik.
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.Entities:
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Year: 1982 PMID: 6120930 PMCID: PMC220101 DOI: 10.1128/jb.150.1.214-220.1982
Source DB: PubMed Journal: J Bacteriol ISSN: 0021-9193 Impact factor: 3.490