Literature DB >> 8885395

Functional definition of regions necessary for replication and incompatibility in the Mycobacterium fortuitum plasmid pAL5000.

P Stolt1, N G Stoker.   

Abstract

Different parts of the Mycobacterium fortuitum plasmid pAL5000 necessary for plasmid replication and incompatibility were defined and studied. Two ORFs, named repA and repB, were defined which are necessary for replication. A pAL5000 derivative deleted in these genes can be made to replicate by providing the gene products in trans. A 435 bp fragment was defined which was necessary in cis for replication and which had an influence on copy number. This region (inc), which contains several repeated motifs, was also able to confer a degree of incompatibility when cloned into an otherwise unrelated mycobacterial replicon. pAL5000-derived plasmids carrying two copies of the inc region had a lower copy number and were less stable than the wild-type. These effects were only observed when the two regions were in the same orientation. Plasmids carrying only the inc region and no other parts of pAL5000 could be made to replicate if repA and repB were supplied in trans from another plasmid. Based on these findings, systems for selectively curing cells of one plasmid of a pair were designed and shown to be functional in Mycobacterium smegmatis. These have potential as a simple delivery system for achieving transposon mutagenesis or gene replacement in mycobacteria.

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Year:  1996        PMID: 8885395     DOI: 10.1099/13500872-142-10-2795

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  26 in total

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Authors:  T Parish; N G Stoker
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Authors:  J A Gavigan; J A Aínsa; E Pérez; I Otal; C Martín
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4.  Efficient transformation system for Propionibacterium freudenreichii based on a novel vector.

Authors:  J P Jore; N van Luijk ; R G Luiten; M J van der Werf ; P H Pouwels
Journal:  Appl Environ Microbiol       Date:  2001-02       Impact factor: 4.792

5.  The F1Fo-ATP synthase of Mycobacterium smegmatis is essential for growth.

Authors:  Sieu L Tran; Gregory M Cook
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6.  Determination of DNA sequences required for regulated Mycobacterium tuberculosis RecA expression in response to DNA-damaging agents suggests that two modes of regulation exist.

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Journal:  J Bacteriol       Date:  1997-06       Impact factor: 3.490

7.  Origin binding activity of the Mycobacterial plasmid pAL5000 replication protein RepB is stimulated through interactions with host factors and coupled expression of repA.

Authors:  Abhijit Basu; Mamta Chawla-Sarkar; Santanu Chakrabarti; Sujoy K Das Gupta
Journal:  J Bacteriol       Date:  2002-04       Impact factor: 3.490

8.  Characterization of the basic replicon of Rhodococcus plasmid pSOX and development of a Rhodococcus-Escherichia coli shuttle vector.

Authors:  C Denis-Larose; H Bergeron; D Labbé; C W Greer; J Hawari; M J Grossman; B M Sankey; P C Lau
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9.  Development of a new generation of vectors for gene expression, gene replacement, and protein-protein interaction studies in mycobacteria.

Authors:  Amit Parikh; Devanand Kumar; Yogesh Chawla; Krishna Kurthkoti; Shazia Khan; Umesh Varshney; Vinay K Nandicoori
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10.  Isolation and characterization of a rolling-circle-type plasmid from Rhodococcus erythropolis and application of the plasmid to multiple-recombinant-protein expression.

Authors:  Nobutaka Nakashima; Tomohiro Tamura
Journal:  Appl Environ Microbiol       Date:  2004-09       Impact factor: 4.792

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