Literature DB >> 1406271

Polyphosphate-selective porin OprO of Pseudomonas aeruginosa: expression, purification and sequence.

R J Siehnel1, C Egli, R E Hancock.   

Abstract

The oprO gene of Pseudomonas aeruginosa codes for a polyphosphate-specific porin and terminates 458 bp upstream of the start codon for the phosphate-specific porin OprP. OprO was found to be expressed only under phosphate-starvation conditions in both wild-type and oprP::Tn501 mutant P. aeruginosa strains. However, unlike the rest of the genes of the Pho regulon, including oprP, expression of oprO required cells to be in the stationary growth phase in addition to phosphate starvation. Wild-type P. aeruginosa cells were grown in fermentor culture under these conditions and fractionated by selective solubilization in octylpolyoxyethylene detergent solution. Solubilized OprO was separated from OprP by application to a Mono Q FPLC column and elution with a salt gradient and shown to be functionally identical to cloned OprO produced in Escherichia coli. DNA sequencing of oprO showed the gene product to be highly homologous to OprP, with 76% identity and 16% conserved substitutions. Most genes of the Pho regulon possess a modified -35 region called the Pho box. Two such elements, separated by 4 bp were found in oprO. DNA sequencing also revealed a second Pho box in the oprP gene with the same spacing.

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Year:  1992        PMID: 1406271     DOI: 10.1111/j.1365-2958.1992.tb01407.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  17 in total

Review 1.  Molecular basis of bacterial outer membrane permeability revisited.

Authors:  Hiroshi Nikaido
Journal:  Microbiol Mol Biol Rev       Date:  2003-12       Impact factor: 11.056

2.  Transcriptome analysis of Pseudomonas aeruginosa after interaction with human airway epithelial cells.

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3.  Structure, Dynamics, and Substrate Specificity of the OprO Porin from Pseudomonas aeruginosa.

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Journal:  Biophys J       Date:  2015-10-06       Impact factor: 4.033

4.  Characterization of OpdH, a Pseudomonas aeruginosa porin involved in the uptake of tricarboxylates.

Authors:  Sandeep Tamber; Elke Maier; Roland Benz; Robert E W Hancock
Journal:  J Bacteriol       Date:  2006-11-17       Impact factor: 3.490

5.  Insertion mutagenesis of the Pseudomonas aeruginosa phosphate-specific porin OprP.

Authors:  A Sukhan; R E Hancock
Journal:  J Bacteriol       Date:  1995-09       Impact factor: 3.490

6.  Distribution of metabolic activity and phosphate starvation response of lux-tagged Pseudomonas fluorescens reporter bacteria in the barley rhizosphere.

Authors:  L Kragelund; C Hosbond; O Nybroe
Journal:  Appl Environ Microbiol       Date:  1997-12       Impact factor: 4.792

7.  Purification and partial characterization of the OmpA family of proteins of Pasteurella haemolytica.

Authors:  P J Mahasreshti; G L Murphy; J H Wyckoff; S Farmer; R E Hancock; A W Confer
Journal:  Infect Immun       Date:  1997-01       Impact factor: 3.441

8.  Siderophore activity of myo-inositol hexakisphosphate in Pseudomonas aeruginosa.

Authors:  A W Smith; D R Poyner; H K Hughes; P A Lambert
Journal:  J Bacteriol       Date:  1994-06       Impact factor: 3.490

9.  Pseudomonas aeruginosa fur overlaps with a gene encoding a novel outer membrane lipoprotein, OmlA.

Authors:  U A Ochsner; A I Vasil; Z Johnson; M L Vasil
Journal:  J Bacteriol       Date:  1999-02       Impact factor: 3.490

10.  The OprB porin plays a central role in carbohydrate uptake in Pseudomonas aeruginosa.

Authors:  J L Wylie; E A Worobec
Journal:  J Bacteriol       Date:  1995-06       Impact factor: 3.490

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