THE HOST-RANGE OF RK2 MINIMAL REPLICON COPY-UP MUTANTS IS LIMITED BY SPECIES-SPECIFIC DIFFERENCES IN THE MAXIMUM TOLERABLE COPY NUMBER

Citation
K. Haugan et al., THE HOST-RANGE OF RK2 MINIMAL REPLICON COPY-UP MUTANTS IS LIMITED BY SPECIES-SPECIFIC DIFFERENCES IN THE MAXIMUM TOLERABLE COPY NUMBER, Plasmid, 33(1), 1995, pp. 27-39
Citations number
36
Categorie Soggetti
Genetics & Heredity
Journal title
ISSN journal
0147619X
Volume
33
Issue
1
Year of publication
1995
Pages
27 - 39
Database
ISI
SICI code
0147-619X(1995)33:1<27:THORMR>2.0.ZU;2-A
Abstract
The minimal replicon of the broad-host-range plasmid RK2 consists of a gene, trfA (trans-acting replication), encoding a protein required fo r initiation of plasmid replication. The TrfA protein binds to iterons in the cis-acting origin of vegetative replication (oriV), but the ex act mechanism by which TrfA-mediated replication initiation takes plac e is not known. We report here the isolation and characterization of f ive mini RK2 trfA mutant plasmids with an elevated plasmid copy number , four in Pseudomonas aeruginosa and one in Azotobacter vinelandii. Th e mutations are localized between or downstream of previously reported Escherichia coli copy-up mutations in trfA, and one of the mutations has been described earlier as an independent copy-up isolate in E. col i. The five mutant plasmids were all moderately copy up in both E. col i and their host of origin, in spite of the use of isolation procedure s which were expected to select efficiently in favor of plasmid mutant s specifying high copy numbers. In contrast, previously described high copy-up mutants isolated in E. coli could not be established in P. ae ruginosa and A. vinelandii. These high copy-up mutants were shown to i nduce cell killing in E. coli under conditions where the plasmid copy number was increased as a physiological response to reduced growth rat e. We propose that the reason for this killing effect is that the copy number under these conditions exceeds an upper tolerance level specif ic for E. coli. By assuming that the corresponding tolerance level is lower in P. aeruginosa and A. vinelandii than in E. coli, and that the mechanism of copy number regulation is similar, the model can explain the phenotypes of all tested copy up mutants in these two hosts. Anal ogous studies were also performed in Salmonella typhimurium and Acetob acter xylinum. The data obtained in these studies indicate that the ab ove model is probably generally true for gram-negative bacteria, and t he results also indicate that the maximum tolerable copy number is sur prisingly low in some hosts. (C) 1995 Academic Press, Inc.