Literature DB >> 804983

Further properties of P-2 R-factors of Pseudomonas aeruginosa and their relationship to other plasmid groups.

M S Shahrabadi, L E Bryan, H M Van Den Elizen.   

Abstract

R-factors of the P-2(prototype R-factor R931) incompatibility group of plasmidsdetected in Pseudomonas are compatible with group P,C,W, and NR-factors which areplasmids that can be transferred to Pseudomonas aeruginosa recipients. Members of the P-2 group (R130,R931) have significant homology by DNA-DNA hybridization. R-factors of the P-group (RP1, RP9) and F-group (R1) exhibited homology with P-2 R-factors but to a lesser extent than R130 with R931. Members of the I, C, and W groups showed no significant homology with P-2 R-factors. Minicircular DNA of strain 931(R931) was not homologous with R931 DNA. The host range of R931 and R130 is limited mainly to certain Pseudomonas species including P. aeruginosa, P. fluorescens, P. putida, and P. stutzeri. These R-factors could not be transferredat detectable frequencies to any member of the Enterobacteriaceae examined. R-factor-specified pili were strongly suggested by the detection of pili by electron microscopyin R-+ but not R- non-piliated mutants of P. aeruginosa strain PA01. The combinedproperties of R-factors 931 and similar R-factors reported before and in this study strongly support our previous contention that this group of R-factors form a significant new group of plasmids. A classification scheme previously proposed for plasmids occurring in Pseudomonas has been modified and four groups have been specified.

Entities:  

Mesh:

Substances:

Year:  1975        PMID: 804983     DOI: 10.1139/m75-086

Source DB:  PubMed          Journal:  Can J Microbiol        ISSN: 0008-4166            Impact factor:   2.419


  16 in total

1.  Bacterial mutation affecting plasmid maintenance in Pseudomonas aeruginosa.

Authors:  B J Chang; B W Holloway
Journal:  J Bacteriol       Date:  1977-05       Impact factor: 3.490

2.  Mechanism of aminoglycoside antibiotic resistance in anaerobic bacteria: Clostridium perfringens and Bacteroides fragilis.

Authors:  L E Bryan; S K Kowand; H M Van Den Elzen
Journal:  Antimicrob Agents Chemother       Date:  1979-01       Impact factor: 5.191

3.  A molecular analysis of transductional marker rescue involving P-group plasmids in Pseudomonas aeruginosa.

Authors:  V A Stanisich; P M Bennett; J M Oritz
Journal:  Mol Gen Genet       Date:  1976-02-02

4.  Spread of a "Pseudomonas-specific" beta-lactamase to plasmids of enterobacteria.

Authors:  A A Medeiros; R W Hedges; G A Jacoby
Journal:  J Bacteriol       Date:  1982-02       Impact factor: 3.490

5.  Characterization of a translocation unit encoding resistance to mercuric ions that occurs on a nonconjugative plasmid in Pseudomonas aeruginosa.

Authors:  V A Stanisich; P M Bennett; M H Richmond
Journal:  J Bacteriol       Date:  1977-03       Impact factor: 3.490

6.  The properties of hybrids formed between the P-group plasmid RP1 and various plasmids from Pseudomonas aeruginosa.

Authors:  V A Stanisich; P M Bennett
Journal:  Mol Gen Genet       Date:  1976-12-08

7.  Interaction of Pseudomonas and Enterobacteriaceae plasmids in Aeromonas salmonicida.

Authors:  R H Olsen; C D Wright
Journal:  J Bacteriol       Date:  1976-10       Impact factor: 3.490

8.  Classification of R plasmids by incompatibility in Pseudomonas aeruginosa.

Authors:  H Sagai; K Hasuda; S Iyobe; L E Bryan; B W Holloway; S Mitsuhashi
Journal:  Antimicrob Agents Chemother       Date:  1976-10       Impact factor: 5.191

9.  Recombination between plasmids of incompatibility groups P-1 and P-2.

Authors:  G A Jacoby; A E Jacob; R W Hedges
Journal:  J Bacteriol       Date:  1976-09       Impact factor: 3.490

10.  Transfer of plasmids from Escherichia coli to Pseudomonas aeruginosa: characterization of a Pseudomonas aeruginosa mutant with enhanced recipient ability for enterobacterial plasmids.

Authors:  G Tardif; R B Grant
Journal:  Antimicrob Agents Chemother       Date:  1983-08       Impact factor: 5.191

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.