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Energy-coupled transport and signal transduction through the gram-negative outer membrane via TonB-ExbB-ExbD-dependent receptor proteins.
Braun, V.
Afiliação
  • Braun V; Mikrobiologie II, Universität Tübingen, Germany.
FEMS Microbiol Rev ; 16(4): 295-307, 1995 Jul.
Article em En | MEDLINE | ID: mdl-7654405
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.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Membrana Celular / Receptores de Superfície Celular / Proteínas de Escherichia coli / Metabolismo Energético / Bactérias Gram-Negativas Idioma: En Revista: FEMS Microbiol Rev Assunto da revista: MICROBIOLOGIA Ano de publicação: 1995 Tipo de documento: Article País de afiliação: Alemanha
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Membrana Celular / Receptores de Superfície Celular / Proteínas de Escherichia coli / Metabolismo Energético / Bactérias Gram-Negativas Idioma: En Revista: FEMS Microbiol Rev Assunto da revista: MICROBIOLOGIA Ano de publicação: 1995 Tipo de documento: Article País de afiliação: Alemanha