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PMID: 6330026 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Conditionally transposition-defective derivative of Mu d1(Amp Lac).

Journal of bacteriology ·Vol. 159 ·No. 1 ·1984-07-00 ·Pages 130-7

Hughes KT, Roth JR

Abstract

A Mu d1 derivative is described which is useful for genetic manipulation of Mu-lac fusion insertions. A double mutant of the specialized transducing phage Mu d1(Amp Lac c62ts) was isolated which is conditionally defective in transposition ability. The Mu d1 derivative, designated Mu d1-8(Tpn[Am] Amp Lac c62ts), carries mutations which virtually eliminate transposition in strains lacking an amber suppressor. In such strains, the Mu d1-8 prophage behaves like a standard transposon. It can be moved from one strain of Salmonella typhimurium to another by the general transducing phage P22 with almost 100% inheritance of the donor insertion mutation. When introduced into a recipient carrying supD, supE, or supF, 89 to 94% of the Ampr transductants were transpositions of the donor Mu d1-8, from the transduced fragment into new sites. The stability of Mu d1-8 in a wild-type, suppressor-free background was sufficient to permit use of the fusion to select constitutive mutations without prior isolation of deletions to stabilize the fusion. Fusion strains could be grown at elevated temperature without induction of the Mu d prophage. The transposition defect of Mu d1-8 was corrected by a plasmid carrying the Mu A and B genes.

MeSH Terms
DNA Restriction Enzymes DNA Transposable Elements Genetic Complementation Test Genotype Mutation Plasmids Salmonella typhimurium/genetics Species Specificity Transduction, Genetic
Chemicals
DNA Transposable Elements DNA Restriction Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hughes K T
Roth J R
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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
1984-07-00
Pages
130-7
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC215603
Subset
IM
Grants
NIGMS NIH HHS · GM 23408 · United States
NIGMS NIH HHS · T32-GM 07464-07 · United States
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