Literature DB >> 8323941

Anion transport through the phosphate-specific OprP-channel of the Pseudomonas aeruginosa outer membrane: effects of phosphate, di- and tribasic anions and of negatively-charged lipids.

R Benz1, C Egli, R E Hancock.   

Abstract

The mechanism of anion transport through the phosphate-starvation inducible OprP-channel of Pseudomonas aeruginosa outer membrane was studied in planar lipid bilayer membranes. The single-channel conductance of OprP was 160 pS in 100 mM chloride solution. Addition of other anions, in particular of phosphate, di and tribasic anions lead to a strong decrease of the chloride conductance. The decrease was used to calculate the stability constants for the binding of these ions to the binding site of the channel on the basis of a one-site two-barrier model. The stability constant of the binding of phosphate to the site was 11,000 M-1 at neutral pH. Surprisingly, di- and tribasic anions, such as sulfate and citrate had a much lower affinity to the binding site inside the channel. Although the single-channel conductance was dependent on the external pH, the stability constants for phosphate binding decrease only slightly for increasing the pH. The use of negatively-charged lipids instead of neutral ones in the planar lipid bilayers had no influence on the single-channel conductance of the OprP-channel, suggesting that the channel is shielded from the influence of surrounding molecules. Its permeability properties are probably not influenced by negatively-charged lipopolysaccharide molecules.

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Year:  1993        PMID: 8323941     DOI: 10.1016/0005-2736(93)90205-e

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  7 in total

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

Authors:  Niraj Modi; Sonalli Ganguly; Iván Bárcena-Uribarri; Roland Benz; Bert van den Berg; Ulrich Kleinekathöfer
Journal:  Biophys J       Date:  2015-10-06       Impact factor: 4.033

2.  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

3.  Protein AQ_1862 from the hyperthermophilic bacterium Aquifex aeolicus is a porin and contains two conductance pathways of different selectivity.

Authors:  Ulrike Wedemeyer; Guohong Peng; Hartmut Michel; Klaus Hartung
Journal:  Biophys J       Date:  2007-06-22       Impact factor: 4.033

Review 4.  Modeling and simulation of ion channels.

Authors:  Christopher Maffeo; Swati Bhattacharya; Jejoong Yoo; David Wells; Aleksei Aksimentiev
Journal:  Chem Rev       Date:  2012-10-04       Impact factor: 60.622

5.  Simulations of anion transport through OprP reveal the molecular basis for high affinity and selectivity for phosphate.

Authors:  Prapasiri Pongprayoon; Oliver Beckstein; Chze Ling Wee; Mark S P Sansom
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-04       Impact factor: 11.205

6.  Characterization of a Novel Porin-Like Protein, ExtI, from Geobacter sulfurreducens and Its Implication in the Reduction of Selenite and Tellurite.

Authors:  Mst Ishrat Jahan; Ryuta Tobe; Hisaaki Mihara
Journal:  Int J Mol Sci       Date:  2018-03-11       Impact factor: 5.923

7.  Properties and Phylogeny of 76 Families of Bacterial and Eukaryotic Organellar Outer Membrane Pore-Forming Proteins.

Authors:  Bhaskara L Reddy; Milton H Saier
Journal:  PLoS One       Date:  2016-04-11       Impact factor: 3.240

  7 in total

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