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PMID: 6193096 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Promoter for the unc operon of Escherichia coli.

Journal of bacteriology ·Vol. 155 ·No. 3 ·1983-09-00 ·Pages 1271-8

Porter AC, Brusilow WS, Simoni RD

Abstract

Fragments of DNA carrying possible promoters for the unc operon of Escherichia coli were cloned into a promoter detection plasmid (pRZ5255). Similar fragments were transcribed in vitro to produce transcripts whose sizes were used to determine the approximate start site for transcription. One strong promoter and at least two very much weaker ones were detected by these methods. The exact position of the strongest promoter, presumed to be the true unc promoter, was determined by S1 nuclease mapping and shown to lie 73 base pairs upstream from the open reading frame that precedes uncB. It therefore appears that this reading frame (uncI) is part of the unc operon. S1 mapping also revealed the presence of a third weak promoter 25 base pairs upstream of uncI. All of the weak promoters occur between the proposed unc promoter and uncB, but their role in vivo, if any, is unclear.

MeSH Terms
Adenosine Triphosphatases/genetics Cloning, Molecular Endonucleases Escherichia coli/enzymology,genetics Genes, Bacterial Operon Plasmids Proton-Translocating ATPases RNA, Bacterial/analysis RNA, Messenger/analysis Single-Strand Specific DNA and RNA Endonucleases Transcription, Genetic
Chemicals
RNA, Bacterial RNA, Messenger Endonucleases Single-Strand Specific DNA and RNA Endonucleases Adenosine Triphosphatases Proton-Translocating ATPases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Porter A C
Brusilow W S
Simoni R D
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31 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1983-09-00
Pages
1271-8
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC217825
Subset
IM
Grants
NIGMS NIH HHS · GM07598 · United States
NIGMS NIH HHS · GM18539 · United States
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