Literature DB >> 3525520

Genetic organization of plasmid R1162 DNA involved in conjugative mobilization.

M A Brasch, R J Meyer.   

Abstract

DNA involved in the mobilization of broad-host-range plasmid R1162 was localized to a region of 2.7 kilobases within coordinates 3.4 to 6.1 kilobases on the R1162 map. By examining the transfer properties of plasmids containing cloned fragments of DNA from within this region, we showed that at least four trans-active products and a cis-active site (oriT) were involved in mobilization. A cloned DNA fragment of 155 base pairs was capable of providing full oriT activity. This fragment was located within 600 base pairs of DNA containing the origin of replication of R1162, and its nucleotide sequence and that of neighboring DNA were determined. Activation of oriT required R1162-encoded, trans-acting products. Deletions which resulted in the loss of one or more of these had a variable effect on transfer efficiency and indicated the presence of both essential and nonessential Mob products. Regions encoding these products flanked oriT and in one case appeared to overlap a gene essential for plasmid replication. The implications of these findings with respect to the broad host range of R1162 are discussed.

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Year:  1986        PMID: 3525520      PMCID: PMC212946          DOI: 10.1128/jb.167.2.703-710.1986

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  35 in total

Review 1.  The conjugation system of F-like plasmids.

Authors:  N Willetts; R Skurray
Journal:  Annu Rev Genet       Date:  1980       Impact factor: 16.830

2.  Temperature-sensitive copy number mutants of CoIE1 are located in an untranslated region of the plasmid genome.

Authors:  E M Wong; M A Muesing; B Polisky
Journal:  Proc Natl Acad Sci U S A       Date:  1982-06       Impact factor: 11.205

3.  A procedure for the large-scale isolation of highly purified plasmid DNA using alkaline extraction and binding to glass powder.

Authors:  M A Marko; R Chipperfield; H C Birnboim
Journal:  Anal Biochem       Date:  1982-04       Impact factor: 3.365

4.  Overlapping genes at the DNA primase locus of the large plasmid ColI.

Authors:  G J Boulnois; B M Wilkins; E Lanka
Journal:  Nucleic Acids Res       Date:  1982-02-11       Impact factor: 16.971

5.  A new pair of M13 vectors for selecting either DNA strand of double-digest restriction fragments.

Authors:  J Messing; J Vieira
Journal:  Gene       Date:  1982-10       Impact factor: 3.688

6.  Construction of improved M13 vectors using oligodeoxynucleotide-directed mutagenesis.

Authors:  J Norrander; T Kempe; J Messing
Journal:  Gene       Date:  1983-12       Impact factor: 3.688

7.  Location of two relaxation nick sites in R6K and single sites in pSC101 and RSF1010 close to origins of vegetative replication: implication for conjugal transfer of plasmid deoxyribonucleic acid.

Authors:  A Nordheim; T Hashimoto-Gotoh; K N Timmis
Journal:  J Bacteriol       Date:  1980-12       Impact factor: 3.490

8.  Vectors bearing a hybrid trp-lac promoter useful for regulated expression of cloned genes in Escherichia coli.

Authors:  E Amann; J Brosius; M Ptashne
Journal:  Gene       Date:  1983-11       Impact factor: 3.688

9.  Properties of R1162, a broad-host-range, high-copy-number plasmid.

Authors:  R Meyer; M Hinds; M Brasch
Journal:  J Bacteriol       Date:  1982-05       Impact factor: 3.490

10.  Plasmid RP4 specifies a deoxyribonucleic acid primase involved in its conjugal transfer and maintenance.

Authors:  E Lanka; P T Barth
Journal:  J Bacteriol       Date:  1981-12       Impact factor: 3.490

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  24 in total

1.  Exploitation of plasmid pMRC01 to direct transfer of mobilizable plasmids into commercial lactococcal starter strains.

Authors:  R M Hickey; D P Twomey; R P Ross; C Hill
Journal:  Appl Environ Microbiol       Date:  2001-06       Impact factor: 4.792

2.  Isolation and screening of plasmids from the epilithon which mobilize recombinant plasmid pD10.

Authors:  K E Hill; A J Weightman; J C Fry
Journal:  Appl Environ Microbiol       Date:  1992-04       Impact factor: 4.792

3.  MobB protein stimulates nicking at the R1162 origin of transfer by increasing the proportion of complexed plasmid DNA.

Authors:  T Perwez; R Meyer
Journal:  J Bacteriol       Date:  1996-10       Impact factor: 3.490

4.  Functional organization of MobB, a small protein required for efficient conjugal transfer of plasmid R1162.

Authors:  Richard Meyer
Journal:  J Bacteriol       Date:  2011-05-27       Impact factor: 3.490

5.  Conjugal mobilization of streptococcal plasmid pMV158 between strains of Lactococcus lactis subsp. lactis.

Authors:  D van der Lelie; H A Wösten; S Bron; L Oskam; G Venema
Journal:  J Bacteriol       Date:  1990-01       Impact factor: 3.490

6.  The MobA-linked primase is the only replication protein of R1162 required for conjugal mobilization.

Authors:  D Henderson; R Meyer
Journal:  J Bacteriol       Date:  1999-05       Impact factor: 3.490

7.  Stabilization of the relaxosome and stimulation of conjugal transfer are genetically distinct functions of the R1162 protein MobB.

Authors:  T Perwez; R J Meyer
Journal:  J Bacteriol       Date:  1999-04       Impact factor: 3.490

8.  Mapping Type IV Secretion Signals on the Primase Encoded by the Broad-Host-Range Plasmid R1162 (RSF1010).

Authors:  Richard Meyer
Journal:  J Bacteriol       Date:  2015-08-03       Impact factor: 3.490

9.  Specific binding of MobA, a plasmid-encoded protein involved in the initiation and termination of conjugal DNA transfer, to single-stranded oriT DNA.

Authors:  M K Bhattacharjee; R J Meyer
Journal:  Nucleic Acids Res       Date:  1993-09-25       Impact factor: 16.971

10.  Relaxed specificity of the R1162 nickase: a model for evolution of a system for conjugative mobilization of plasmids.

Authors:  Eric C Becker; Richard J Meyer
Journal:  J Bacteriol       Date:  2003-06       Impact factor: 3.490

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