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PMID: 6187472 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Insertion of IS2 creates a novel ampC promoter in Escherichia coli.

Cell ·Vol. 32 ·No. 3 ·1983-03-00 ·Pages 809-16

Jaurin B, Normark S

Abstract

A class of ampC beta-lactamase-hyperproducing mutants of Escherichia coli were shown to have the insertion element IS2 inserted into the ampC promoter. The insertion of IS2 in orientation II created a novel promoter in which the -35 region and the 17 bp long spacing sequence between the two consensus sequences are present in IS2 DNA, whereas the -10 region from the original ampC promoter is retained. In vitro transcription revealed that the transcription initiation site in the ampC::IS2 mutants was identical with that of ampC wild-type promoter. The novel promoter exhibited a 20-fold increase in promoter strength relative to the original ampC promoter, presumably due to the increase in the spacing sequence from 16 to 17 bp. The evolution of transposable elements and of control elements such as promoters are discussed on the basis of the findings described herein.

MeSH Terms
Base Sequence DNA Transposable Elements DNA, Bacterial/analysis Escherichia coli/enzymology,genetics Gene Expression Regulation Mutation Operon Protein Biosynthesis RNA, Bacterial/metabolism beta-Lactamases/biosynthesis
Chemicals
DNA Transposable Elements DNA, Bacterial RNA, Bacterial beta-Lactamases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Jaurin B
Normark S
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1983-03-00
Pages
809-16
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Databases
GENBANK
J01583, J01584, J01585, J01611
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