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PMID: 7654405 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Energy-coupled transport and signal transduction through the gram-negative outer membrane via TonB-ExbB-ExbD-dependent receptor proteins.

FEMS microbiology reviews ·Vol. 16 ·No. 4 ·1995-07-00 ·Pages 295-307

Braun V

Abstract

Iron in the form of ferric siderophore complexes and vitamin B12 are transported through the outer membrane of Gram-negative bacteria by a mechanism which consumes energy. There is no known energy source in the outer membrane or in the adjacent periplasmic space so that energy is provided by the electrochemical potential across the cytoplasmic membrane. Energy flows from the cytoplasmic into the outer membrane via a complex consisting of the TonB, ExbB and ExbD proteins which are anchored in the cytoplasmic membrane. It is proposed that the TonB--ExbB--ExbD complex opens--via an energized conformation of the TonB protein--channels in the outer membrane, formed by proteins which serves as highly specific binding sites for the various ferric siderophores and vitamin B12. In addition, outer membrane receptors together with the TonB--ExbB--ExbD complex are directly involved in induction of the transcription of ferric citrate and pseudobactin transport genes of Escherichia coli and Pseudomonas putida, respectively.

MeSH Terms
Amino Acid Sequence Bacterial Proteins/metabolism Biological Transport/physiology Cell Membrane/physiology Colicins/metabolism Energy Metabolism Escherichia coli Proteins Ferric Compounds/metabolism Gram-Negative Bacteria/physiology Membrane Proteins/metabolism Molecular Sequence Data Receptors, Cell Surface/metabolism Siderophores/metabolism Signal Transduction/physiology Vitamin B 12/metabolism
Chemicals
Bacterial Proteins Colicins Escherichia coli Proteins ExbB protein, E coli Ferric Compounds Membrane Proteins Receptors, Cell Surface Siderophores tonB protein, Bacteria tonB protein, E coli exbD protein, E coli Vitamin B 12
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Braun V
Mikrobiologie II, Universität Tübingen, Germany.
Article Info
Journal
FEMS microbiology reviews
Abbr.
FEMS Microbiol Rev
ISSN
0168-6445
Published
1995-07-00
Pages
295-307
Language
English
Region
England
NLM ID
8902526
Subset
IM
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