Literature DB >> 11698385

Controlled expression in Klebsiella pneumoniae and Shigella flexneri using a bacteriophage P1-derived C1-regulated promoter system.

D A Schofield1, C Westwater, J W Dolan, M G Schmidt, J S Norris.   

Abstract

The utility of promoters regulated by the bacteriophage P1 temperature-sensitive C1 repressor was examined in Shigella flexneri and Klebsiella pneumoniae. Promoters carrying C1 operator sites driving LacZ expression had induction/repression ratios of up to 240-fold in S. flexneri and up to 50-fold in K. pneumoniae. The promoters exhibited remarkably low basal expression, demonstrated modulation by temperature, and showed rapid induction. This system will provide a new opportunity for controlled gene expression in enteric gram-negative bacteria.

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Year:  2001        PMID: 11698385      PMCID: PMC95537          DOI: 10.1128/JB.183.23.6947-6950.2001

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


  27 in total

1.  ban operon of bacteriophage P1. Mutational analysis of the c1 repressor-controlled operator.

Authors:  T Heinzel; M Velleman; H Schuster
Journal:  J Mol Biol       Date:  1989-01-05       Impact factor: 5.469

2.  Three additional operators, Op21, Op68, and Op88, of bacteriophage P1. Evidence for control of the P1 dam methylase by Op68.

Authors:  M Citron; M Velleman; H Schuster
Journal:  J Biol Chem       Date:  1989-02-25       Impact factor: 5.157

3.  Multiple repressor binding sites in the genome of bacteriophage P1.

Authors:  M Velleman; B Dreiseikelmann; H Schuster
Journal:  Proc Natl Acad Sci U S A       Date:  1987-08       Impact factor: 11.205

4.  Construction of multicopy expression vectors for regulated over-production of proteins in Klebsiella pneumoniae and other enteric bacteria.

Authors:  D Kleiner; W Paul; M J Merrick
Journal:  J Gen Microbiol       Date:  1988-07

5.  Characterization of the binding sites of c1 repressor of bacteriophage P1. Evidence for multiple asymmetric sites.

Authors:  J L Eliason; N Sternberg
Journal:  J Mol Biol       Date:  1987-11-20       Impact factor: 5.469

6.  Expansion of the host range of coliphage P1 and gene transfer from enteric bacteria to other gram-negative bacteria.

Authors:  Y Murooka; T Harada
Journal:  Appl Environ Microbiol       Date:  1979-10       Impact factor: 4.792

7.  Plasmid vectors for high-efficiency expression controlled by the PL promoter of coliphage lambda.

Authors:  E Remaut; P Stanssens; W Fiers
Journal:  Gene       Date:  1981-10       Impact factor: 3.688

8.  The c1 repressor inactivator protein coi of bacteriophage P1. Cloning and expression of coi and its interference with c1 repressor function.

Authors:  T Heinzel; M Velleman; H Schuster
Journal:  J Biol Chem       Date:  1990-10-15       Impact factor: 5.157

9.  A rapid and efficient method for plasmid transformation of Klebsiella pneumoniae and Escherichia coli.

Authors:  M J Merrick; J R Gibbins; J R Postgate
Journal:  J Gen Microbiol       Date:  1987-08

10.  The ImmC region of phage P1 codes for a gene whose product promotes lytic growth.

Authors:  B R Baumstark; S R Stovall; P Bralley
Journal:  Virology       Date:  1990-11       Impact factor: 3.616

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  2 in total

1.  Use of genetically engineered phage to deliver antimicrobial agents to bacteria: an alternative therapy for treatment of bacterial infections.

Authors:  Caroline Westwater; Laura M Kasman; David A Schofield; Phillip A Werner; Joseph W Dolan; Michael G Schmidt; James S Norris
Journal:  Antimicrob Agents Chemother       Date:  2003-04       Impact factor: 5.191

2.  Development of a thermally regulated broad-spectrum promoter system for use in pathogenic gram-positive species.

Authors:  David A Schofield; Caroline Westwater; Brian D Hoel; Phillip A Werner; James S Norris; Michael G Schmidt
Journal:  Appl Environ Microbiol       Date:  2003-06       Impact factor: 4.792

  2 in total

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