Abstract
lon mutants of Escherichia coli K-12 are defective in an ATP-dependent protease, are UV sensitive, and overproduce the capsular polysaccharide colanic acid. Six structural genes needed for capsular polysaccharide synthesis (cps) are transcriptionally regulated by lon as well as by three other regulatory genes, rcsA, -B, and -C (S. Gottesman, P. Trisler, and A. S. Torres-Cabassa, J. Bacteriol. 162:1111-1119, 1985). We have cloned rcsA, the gene for a positive regulator of capsule synthesis, onto multicopy plasmids and defined the gene by both insertions and deletions. The product of rcsA has been identified as an unstable protein of 27 kilodaltons. RcsA has a half-life of 5 min in lon+ cells and one of 20 min in lon cells. The availability of RcsA is the limiting factor for capsule synthesis; doubling the gene dosage of rcsA+ significantly increases expression of cps genes. Our results are consistent with a model in which the presence of a lon mutation increases the synthesis of capsular polysaccharide via stabilization of RcsA.
MeSH Terms
ATP-Dependent Proteases
Chromosome Deletion
DNA Restriction Enzymes
Endopeptidases/genetics,metabolism
Escherichia coli/genetics,metabolism
Escherichia coli Proteins
Gene Expression Regulation
Genes
Genes, Bacterial
Genes, Regulator
Genotype
Heat-Shock Proteins
Mutation
Plasmids
Protease La
Serine Endopeptidases
Transcription, Genetic
Chemicals
Escherichia coli Proteins
Heat-Shock Proteins
DNA Restriction Enzymes
Endopeptidases
ATP-Dependent Proteases
Serine Endopeptidases
Lon protein, E coli
Protease La
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Torres-Cabassa A S
Gottesman S
References (29)
29 references, click to expand
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