Iron metabolism in pathogenic bacteria.
By C. Ratledge, L. Dover. Annual Review of Microbiology, 2000
1,543 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology, Molecular Medicine
View Paper: https://www.semanticscholar.org/paper/08aa87427c9ae4a2ba113835430f6ad682c29336
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Genetics
- Andy Gardner
- Stuart A. West
- A. Griffin
- S. Gottesman
- Steve Diggle
- Freddy E. Escorcia
- Angus Buckling
- Mohamed A. Marahiel
In Molecular Biology
- S. Gottesman
- Freddy E. Escorcia
- Mohamed A. Marahiel
- Eric P. Skaar
- É. Massé
- Shintaro Sato
- Stuart A. West
- C. Walsh
In Molecular Medicine
Citations in the corpus
- Dangerous liaisons: The symbiosis of entomopathogenic nematodes and bacteria (2006, background): “TbpA interacts with a surface-exposed iron-binding lipoprotein, TbpB required for iron utilization (Ratledge and Dover, 2000).”
- Lipocalin 2 mediates an innate immune response to bacterial infection by sequestrating iron (2004, background): “During infection, bacteria acquire much of their iron from the host by synthesizing siderophores that scavenge iron and transport it into the pathoge”
- Signals, Regulatory Networks, and Materials That Build and Break Bacterial Biofilms (2009, background): “This effect is dependent on the ferric uptake repressor Fur, a global repressor of gene transcription in iron-rich environments found in P. aeruginosa and other members of the Proteobacteria (262, 330).”
- The Battle for Iron between Bacterial Pathogens and Their Vertebrate Hosts (2010, background): “tribute to the virulence of both animal and plant pathogens [7].”
- Siderophore-Based Iron Acquisition and Pathogen Control (2007, background): “tuberculosis and Mycobacterium leprae, however, apparently use the same genes to synthesize mycobactin derivatives called carboxymycobactins, which possess a shorter carboxyalkyl chain that renders them more hydrophilic with respect to their function as extracellular siderophores (268).”
- Coupled degradation of a small regulatory RNA and its mRNA targets in Escherichia coli. (2003, background): “Accessible iron is very scarce in many environments, particularly for bacteria in mammalian hosts (Ratledge and Dover 2000).”
- Social evolution theory for microorganisms (2006, background): “For example, there is facultative variation in response to environmental conditions, such as in the amount of siderophore productio”
- Review: microbial mechanisms of accessing insoluble Fe(III) as an energy source (2003, background): “They are water-soluble, low molecular weight (500–1000 Da), Fe(III)-specific ligands which are induced at low iron concentrations (Guerinot 1994; Ratledge & Dover 2000 ).”
- Genetics and Assembly Line Enzymology of Siderophore Biosynthesis in Bacteria (2002, background): “plex by the outer membrane protein receptors (10, 12, 26, 90).”
- Structure and function of the spleen (2005, background): “Several pathogens compete for iron in serum and tissue by secreting SIDEROPHORES , which are molecules with a high affinity for iron, and these molecules are transported back into bacteria by specific receptor”
- The Social Lives of Microbes (2007, background): “Siderophores are iron-scavenging molecules produced by many species of bacteria (Ratledge & Dover 2000, West & Buckling 2003).”
- The neutrophil lipocalin NGAL is a bacteriostatic agent that interferes with siderophore-mediated iron acquisition. (2002, background): “…and shape of the anomalous peak bacterial siderophores bind iron orders of magnitude more tightly than lactoferrin or transferrin, directly out-suggested that the chromophore contained a single heavy atom. competing these mammalian proteins for iron during infection (Ratledge and Dover, 2000).”