Abstract
Polyacrylamide gel analysis of [35S]methionine-labeled membrane preparations from Escherichia coli has revealed the presence of five polypeptides present only in the membranes of cells containing the conjugative plasmid F. In addition to the previously reported product of traT, polypeptides migrating with apparent molecular weights of 100,000, 23,500, 12,000, and 7,000 were resolved. Membrane preparations from F traJ mutants lacked these polypeptides, indicating that all of these proteins are tra gene products. The 7,000-molecular-weight polypeptide comigrated with unlabeled purified F-pilin protein. About 4 to 5% of the total radioactive label in whole membrane preparations was present in this polypeptide, indicating the existence of a substantial pool of membrane-associated F-pilin. The polypeptide could be extracted from whole membrane preparations with Triton X-100 and was found in the inner membrane fraction of membranes separated by sucrose density centrifugation.
MeSH Terms
Autoradiography
Cell Membrane/analysis
Electrophoresis, Polyacrylamide Gel
Escherichia coli/genetics,ultrastructure
Escherichia coli Proteins
Fimbriae Proteins
Fimbriae, Bacterial
Membrane Proteins/metabolism
Mutation
Octoxynol
Polyethylene Glycols
Chemicals
Escherichia coli Proteins
F pilin, E coli
Membrane Proteins
Fimbriae Proteins
Polyethylene Glycols
Octoxynol
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Moore D
Sowa B A
Ippen-Ihler K
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25 references, click to expand
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