Literature DB >> 11123683

Emerging strategies in microbial haem capture.

C A Genco1, D W Dixon.   

Abstract

Gram-negative pathogenic bacteria have evolved novel strategies to obtain iron from host haem-sequestering proteins. These include the production of specific outer membrane receptors that bind directly to host haem-sequestering proteins, secreted haem-binding proteins (haemophores) that bind haem/haemoglobin/haemopexin and deliver the complex to a bacterial cell surface receptor and bacterial proteases that degrade haem-sequestering proteins. Once removed from haem-sequestering proteins, haem may be transported via the bacterial outer membrane receptor into the cell. Recent studies have begun to define the steps by which haem is removed from bacterial haem proteins and transported into the cell. This review describes recent work on the discovery and characterization of these systems. Reference is also made to the transport of haem in serum (via haemoglobin, haemoglobin/haptoglobin, haemopexin, albumin and lipoproteins) and to mechanisms of iron removal from the haem itself (probably via a haem oxygenase pathway in which the protoporphyrin ring is degraded). Haem protein-receptor interactions are discussed in terms of the criteria that govern protein-protein interactions in general, and connections between haem transport and the emerging field of metal transport via metallochaperones are outlined.

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Year:  2001        PMID: 11123683     DOI: 10.1046/j.1365-2958.2001.02231.x

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


  81 in total

1.  The surface-associated and secreted MopE protein of Methylococcus capsulatus (Bath) responds to changes in the concentration of copper in the growth medium.

Authors:  Odd A Karlsen; Frode S Berven; Graham P Stafford; Øivind Larsen; J Colin Murrell; Harald B Jensen; Anne Fjellbirkeland
Journal:  Appl Environ Microbiol       Date:  2003-04       Impact factor: 4.792

2.  HmuP is a coactivator of Irr-dependent expression of heme utilization genes in Bradyrhizobium japonicum.

Authors:  Rosalba Escamilla-Hernandez; Mark R O'Brian
Journal:  J Bacteriol       Date:  2012-04-13       Impact factor: 3.490

3.  Unique host iron utilization mechanisms of Helicobacter pylori revealed with iron-deficient chemically defined media.

Authors:  Olga Senkovich; Shantelle Ceaser; David J McGee; Traci L Testerman
Journal:  Infect Immun       Date:  2010-02-22       Impact factor: 3.441

4.  Shigella dysenteriae ShuS promotes utilization of heme as an iron source and protects against heme toxicity.

Authors:  Elizabeth E Wyckoff; Gregory F Lopreato; Kimberly A Tipton; Shelley M Payne
Journal:  J Bacteriol       Date:  2005-08       Impact factor: 3.490

5.  LuxS involvement in the regulation of genes coding for hemin and iron acquisition systems in Porphyromonas gingivalis.

Authors:  Chloe E James; Yoshiaki Hasegawa; Yoonsuk Park; Vincent Yeung; Gena D Tribble; Masae Kuboniwa; Donald R Demuth; Richard J Lamont
Journal:  Infect Immun       Date:  2006-07       Impact factor: 3.441

6.  Structural characterization of the hemophore HasAp from Pseudomonas aeruginosa: NMR spectroscopy reveals protein-protein interactions between Holo-HasAp and hemoglobin.

Authors:  Aileen Y Alontaga; Juan Carlos Rodriguez; Ernst Schönbrunn; Andreas Becker; Todd Funke; Erik T Yukl; Takahiro Hayashi; Jordan Stobaugh; Pierre Moënne-Loccoz; Mario Rivera
Journal:  Biochemistry       Date:  2009-01-13       Impact factor: 3.162

7.  Heme-responsive transcriptional activation of Bordetella bhu genes.

Authors:  Carin K Vanderpool; Sandra K Armstrong
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

8.  The Ton system, an ABC transporter, and a universally conserved GTPase are involved in iron utilization by Brucella melitensis 16M.

Authors:  Isabelle Danese; Valerie Haine; Rose-May Delrue; Anne Tibor; Pascal Lestrate; Olivier Stevaux; Pascal Mertens; Jean-Yves Paquet; Jacques Godfroid; Xavier De Bolle; Jean-Jacques Letesson
Journal:  Infect Immun       Date:  2004-10       Impact factor: 3.441

9.  A new way to degrade heme: the Mycobacterium tuberculosis enzyme MhuD catalyzes heme degradation without generating CO.

Authors:  Shusuke Nambu; Toshitaka Matsui; Celia W Goulding; Satoshi Takahashi; Masao Ikeda-Saito
Journal:  J Biol Chem       Date:  2013-02-18       Impact factor: 5.157

10.  Function, regulation, and transcriptional organization of the hemin utilization locus of Bartonella quintana.

Authors:  Nermi L Parrow; Jasmin Abbott; Amanda R Lockwood; James M Battisti; Michael F Minnick
Journal:  Infect Immun       Date:  2008-11-03       Impact factor: 3.441

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