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PMID: 97269 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Isolation of large bacterial plasmids and characterization of the P2 incompatibility group plasmids pMG1 and pMG5.

Journal of bacteriology ·Vol. 135 ·No. 1 ·1978-07-00 ·Pages 227-38

Hansen JB, Olsen RH

Abstract

Large plasmids from Agrobacterium tumefaciens, Salmonella typhimurium, Escherichia coli, Pseudomonas putida, and Pseudomonas aeruginosa were routinely and consistently isolated using a procedure which does not require ultracentrifugation but includes steps designed to separate large-plasmid DNA from the bacterial folded chromosome. It also selectively removes fragments of broken chromosome. A variety of large plasmids was readily visualized with agarose gel electorphoresis, including five between 70 and 85 megadaltons (Mdal) in size, six between 90 and 143 Mdal, one that was larger than 200 Mdal, and one that was larger than 300 Mdal. This isolation procedure allowed initial estimation of the molecular sizes of the two IncP2 plasmids, pMG1 and pMG5, which were 312 and 280 Mdal, respectively. A standard curve for size determination by gel electrophoresis including plasmids between 23 and 143 Mdal in size did not extrapolate linearly for plasmids of the 300-Mdal size range. Unique response of different plasmids to the isolation procedure included sensitivity of IncP1 plasmids to high pH and the co-isolation of a 20-Mdal "cryptic" plasmid in conjunction.

MeSH Terms
DNA, Bacterial/analysis,isolation & purification Escherichia coli/genetics Molecular Weight Plasmids Pseudomonas/genetics Pseudomonas aeruginosa/genetics Rhizobium/genetics Salmonella typhimurium/genetics
Chemicals
DNA, Bacterial
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hansen J B
Olsen R H
References (39)
39 references, click to expand
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1978-07-00
Pages
227-38
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC224811
Subset
IM
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