Literature DB >> 11967085

Quantification of known components of the Escherichia coli TonB energy transduction system: TonB, ExbB, ExbD and FepA.

Penelope I Higgs1, Ray A Larsen, Kathleen Postle.   

Abstract

The TonB-dependent energy transduction system couples cytoplasmic membrane proton motive force to active transport of iron-siderophore complexes across the outer membrane in Gram-negative bacteria. In Escherichia coli, the primary players known in this process to date are: FepA, the TonB-gated transporter for the siderophore enterochelin; TonB, the energy-transducing protein; and two cytoplasmic membrane proteins with less defined roles, ExbB and ExbD. In this study, we report the per cell numbers of TonB, ExbB, ExbD and FepA for cells grown under iron-replete and iron-limited conditions. Under iron-replete conditions, TonB and FepA were present at 335 +/- 78 and 504 +/- 165 copies per cell respectively. ExbB and ExbD, despite being encoded from the same operon, were not equimolar, being present at 2463 +/- 522 and 741 +/- 105 copies respectively. The ratio of these proteins was calculated at one TonB:two ExbD:seven ExbB under all four growth conditions tested. In contrast, the TonB:FepA ratio varied with iron status and according to the method used for iron limitation. Differences in the method of iron limitation also resulted in significant differences in cell size, skewing the per cell copy numbers for all proteins.

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Year:  2002        PMID: 11967085     DOI: 10.1046/j.1365-2958.2002.02880.x

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


  60 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.  Performance of standard phenotypic assays for TonB activity, as evaluated by varying the level of functional, wild-type TonB.

Authors:  Ray A Larsen; Gregory J Chen; Kathleen Postle
Journal:  J Bacteriol       Date:  2003-08       Impact factor: 3.490

3.  FepA with globular domain deletions lacks activity.

Authors:  Hema L Vakharia; Kathleen Postle
Journal:  J Bacteriol       Date:  2002-10       Impact factor: 3.490

4.  Point mutations in transmembrane helices 2 and 3 of ExbB and TolQ affect their activities in Escherichia coli K-12.

Authors:  Volkmar Braun; Christina Herrmann
Journal:  J Bacteriol       Date:  2004-07       Impact factor: 3.490

5.  Identification of functionally important TonB-ExbD periplasmic domain interactions in vivo.

Authors:  Anne A Ollis; Kathleen Postle
Journal:  J Bacteriol       Date:  2012-04-06       Impact factor: 3.490

6.  The ExbD periplasmic domain contains distinct functional regions for two stages in TonB energization.

Authors:  Anne A Ollis; Aruna Kumar; Kathleen Postle
Journal:  J Bacteriol       Date:  2012-04-06       Impact factor: 3.490

7.  The same periplasmic ExbD residues mediate in vivo interactions between ExbD homodimers and ExbD-TonB heterodimers.

Authors:  Anne A Ollis; Kathleen Postle
Journal:  J Bacteriol       Date:  2011-10-07       Impact factor: 3.490

8.  Direct measurements of the outer membrane stage of ferric enterobactin transport: postuptake binding.

Authors:  Salete M Newton; Vy Trinh; Hualiang Pi; Phillip E Klebba
Journal:  J Biol Chem       Date:  2010-03-24       Impact factor: 5.157

9.  Cooperative uptake of microcin E492 by receptors FepA, Fiu, and Cir and inhibition by the siderophore enterochelin and its dimeric and trimeric hydrolysis products.

Authors:  Erwin Strahsburger; Marcelo Baeza; Octavio Monasterio; Rosalba Lagos
Journal:  Antimicrob Agents Chemother       Date:  2005-07       Impact factor: 5.191

10.  Stereospecificity of the siderophore pyochelin outer membrane transporters in fluorescent pseudomonads.

Authors:  Françoise Hoegy; Xiaoyun Lee; Sabrina Noel; Didier Rognan; Gaëtan L A Mislin; Cornelia Reimmann; Isabelle J Schalk
Journal:  J Biol Chem       Date:  2009-03-17       Impact factor: 5.157

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