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PMID: 6305912 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Cloning of the pif region of the F sex factor and identification of a pif protein product.

Journal of bacteriology ·Vol. 155 ·No. 1 ·1983-07-00 ·Pages 254-64

Rotman GS, Cooney R, Malamy MH

Abstract

This paper reports a detailed investigation of the pif region of the F factor responsible for inhibition of development of T7 and related "female-specific" phages. We have mapped a series of pif::Tn5 insertions to a region between 39.6 and 42.8 kilobases on the physical map of F. All pif::Tn5 insertions plated T7 at full efficiency; most were clustered in a 1.8-kilobase interval on both sides of the EcoRI site located at F coordinate 40.3 kilobases. A 5.2-kilobase Pst-I fragment with F coordinates 38.9 to 44.1 has been cloned into a pSC101 vector to create the Pif+ plasmid pGS103. A series of Pif- deletion mutants and nonsense mutants were isolated from pGS103. Using minicells carrying pGS103 or its derivatives, we have identified a 70,000-dalton pif protein.

MeSH Terms
Bacterial Proteins/genetics Cloning, Molecular DNA Restriction Enzymes Escherichia coli/genetics,physiology F Factor Genotype Mutation Plasmids
Chemicals
Bacterial Proteins DNA Restriction Enzymes
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Rotman G S
Cooney R
Malamy M H
References (32)
32 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1983-07-00
Pages
254-64
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC217676
Subset
IM
Grants
NIAID NIH HHS · AI 15840 · United States
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