Literature DB >> 19189184

Unconventional integration of the bla gene from plasmid pIT2 during ISlacZ/hah transposon mutagenesis in Pseudomonas aeruginosa PAO1.

Congran Li1, Chung-Dar Lu.   

Abstract

The ISlacZ/hah transposon carried by pIT2 and derived originally from Tn5 has been a popular system in the generation of random insertion mutants of Pseudomonas aeruginosa. Using this system in the current study, two transconjugants were identified as conferring high levels of carbenicillin resistance. Analyses by gene complementation tests and site-specific gene knockout experiments support the conclusion that carbenicillin resistance in these two mutants is not due to the insertion of ISlacZ/hah transposon into the affected genes. Instead, the production of a TEM beta-lactamase was detected, and integration of the bla gene from pIT2 to the chromosome of the recipient strain was confirmed by polymerase chain reaction. This surprising event was reproducible, with an estimated frequency among the transconjugants of 4% to 10%, and it may cause a potential complication in the interpretation of mutant phenotypes without notice.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19189184     DOI: 10.1007/s00284-008-9348-9

Source DB:  PubMed          Journal:  Curr Microbiol        ISSN: 0343-8651            Impact factor:   2.188


  9 in total

1.  Comprehensive transposon mutant library of Pseudomonas aeruginosa.

Authors:  Michael A Jacobs; Ashley Alwood; Iyarit Thaipisuttikul; David Spencer; Eric Haugen; Stephen Ernst; Oliver Will; Rajinder Kaul; Christopher Raymond; Ruth Levy; Liu Chun-Rong; Donald Guenthner; Donald Bovee; Maynard V Olson; Colin Manoil
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-14       Impact factor: 11.205

2.  Polyamines increase antibiotic susceptibility in Pseudomonas aeruginosa.

Authors:  Dong H Kwon; Chung-Dar Lu
Journal:  Antimicrob Agents Chemother       Date:  2006-05       Impact factor: 5.191

3.  The use of analytical isoelectric focusing for detection and identification of beta-lactamases.

Authors:  A Mathew; A M Harris; M J Marshall; G W Ross
Journal:  J Gen Microbiol       Date:  1975-05

4.  Osmotic shock: a mechanosensitive channel blocker can prevent release of cytoplasmic but not periplasmic proteins.

Authors:  Hosam E Ewis; Chung-Dar Lu
Journal:  FEMS Microbiol Lett       Date:  2005-10-13       Impact factor: 2.742

5.  Polyamine effects on antibiotic susceptibility in bacteria.

Authors:  Dong-Hyeon Kwon; Chung-Dar Lu
Journal:  Antimicrob Agents Chemother       Date:  2007-04-16       Impact factor: 5.191

6.  Cloning and characterization of the aru genes encoding enzymes of the catabolic arginine succinyltransferase pathway in Pseudomonas aeruginosa.

Authors:  Y Itoh
Journal:  J Bacteriol       Date:  1997-12       Impact factor: 3.490

7.  The genetic organization of arginine biosynthesis in Pseudomonas aeruginosa.

Authors:  D Haas; B W Holloway; A Schamböck; T Leisinger
Journal:  Mol Gen Genet       Date:  1977-07-07

8.  Escherichia-Pseudomonas shuttle vectors derived from pUC18/19.

Authors:  H P Schweizer
Journal:  Gene       Date:  1991-01-02       Impact factor: 3.688

9.  Cloning and characterization of the Pseudomonas aeruginosa lasR gene, a transcriptional activator of elastase expression.

Authors:  M J Gambello; B H Iglewski
Journal:  J Bacteriol       Date:  1991-05       Impact factor: 3.490

  9 in total
  2 in total

1.  Functional characterization of seven γ-Glutamylpolyamine synthetase genes and the bauRABCD locus for polyamine and β-Alanine utilization in Pseudomonas aeruginosa PAO1.

Authors:  Xiangyu Yao; Weiqing He; Chung-Dar Lu
Journal:  J Bacteriol       Date:  2011-05-27       Impact factor: 3.490

2.  The multifaceted proteins MvaT and MvaU, members of the H-NS family, control arginine metabolism, pyocyanin synthesis, and prophage activation in Pseudomonas aeruginosa PAO1.

Authors:  Congran Li; Hassan Wally; Shearman J Miller; Chung-Dar Lu
Journal:  J Bacteriol       Date:  2009-08-14       Impact factor: 3.490

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.