Abstract
The D-ribose operon (rbs) of Escherichia coli K-12 maps at 83 min and is inducible. The rbs operon of E. coli B/r maps at 2 min and is constitutive. Evidence is presented showing that a second inducible copy of the rbs operons is present in E. coli B/r mapping at 83 min. The data indicated that the duplication of the rbs operon represented a transposition of the 83-min region to 2 min. The identification of a second copy of the rbs operon in B/r and the determination of its inducibility were based on the reactivation, through mutagenesis, of inducible rbs expression, mapping by P1 transduction of the mutation site to 83 min, and merodiploid complementation analysis of the D-ribokinase expression in E. coli B/r. We also show that the rbs transposition to 2-min continued to generate transposable elements coding for the 1- to 2-min region of the chromosome and transposing onto extrachromosomal DNA target molecules such as pBR322.
MeSH Terms
Chromosome Mapping
Chromosomes, Bacterial
DNA Restriction Enzymes
DNA Transposable Elements
Enzyme Induction
Escherichia coli/genetics
Genes, Regulator
Genetic Complementation Test
Operon
Phosphotransferases/biosynthesis
Phosphotransferases (Alcohol Group Acceptor)
Plasmids
Ribose/biosynthesis,metabolism
Transduction, Genetic
Chemicals
DNA Transposable Elements
Ribose
Phosphotransferases
Phosphotransferases (Alcohol Group Acceptor)
ribokinase
DNA Restriction Enzymes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Abou-Sabé M
Pilla J
Hazuda D
Ninfa A
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11 references, click to expand
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