Cited by 568Iron Metabolism and DisordersInorganic and Organometallic ChemistryBacterial Genetics and Biotechnology

The DOI matches its Crossref record; 72 of the 74 references it cites were found in a registry or an index.

Chemical aspects of siderophore mediated iron transport

Boukhalfa, Hakim, Crumbliss, Alvin L.·2002·Biometals

DOI 10.1023/a:1020218608266

Open this paper in CoChat — free account

Abstract

In this mini-review we describe selected aspects of the coordination chemistry relevant to siderophore mediated iron transport and bioavailability. Specific emphasis is placed on a discussion of in vitro kinetic and thermodynamic data that are relevant to elucidating possible in vivo mechanisms for environmental iron acquisition by microbial cells.

Integrity signals

Registry

Crossref · 10.1023/a:1020218608266

Cites

72 of 72 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Critical Stability Constants
Martell, A. E., & Smith, R. M. (1982) · Springer eBooks · doi:10.1007/978-1-4615-6761-5 · Cited by 6,025
Siderophore-Mediated Iron Transport: Crystal Structure of FhuA with Bound Lipopolysaccharide
Ferguson, A. D., Hofmann, E., Coulton, J. W., Diederichs, K., & Welte, W. (1998) · Science · doi:10.1126/science.282.5397.2215 · Cited by 787
Crystal structure of the outer membrane active transporter FepA from Escherichia coli.
Buchanan (1999) · Nature Structural Biology · doi:10.1038/4931 · Cited by 591
Transmembrane Signaling across the Ligand-Gated FhuA Receptor
Locher, K. P., Rees, B., Koebnik, R., Mitschler, A., Moulinier, L., Rosenbusch, J. P., & Moras, D. (1998) · Cell · doi:10.1016/s0092-8674(00)81700-6 · Cited by 540
CRC handbook of microbial iron chelates
Winkelmann, G. (2017) · Medical Entomology and Zoology · Cited by 432
Complexation of iron by siderophores a review of their solution and structural chemistry and biological function
Raymond, K. N., Müller, G., & Matzanke, B. F. (1984) · Topics in Current Chemistry · doi:10.1007/3-540-13099-3_2 · Cited by 357 · cited 2×
“4, 1 μM total Fe3+ and 10 μM total ligand) gives a better evaluation of the differences in ligand affinity for iron (Raymond et al. 1984).”
Influential
Solution equilibria of enterobactin and metal-enterobactin complexes
Loomis, L. D., & Raymond, K. N. (1991) · Inorganic Chemistry · doi:10.1021/ic00005a008 · Cited by 321
Coordination chemistry and microbial iron transport
Raymond, K. N., & Carrano, C. J. (1979) · Accounts of Chemical Research · doi:10.1021/ar50137a004 · Cited by 298
Bacterial iron transport: mechanisms, genetics, and regulation.
Braun, V., Hantke, K., & Köster, W. L. (1998) · PubMed · Cited by 297
Coordination Chemistry of Microbial Iron Transport
Raymond, K. N., Allred, B. E., & Sia, A. K. (2015) · Accounts of Chemical Research · doi:10.1021/acs.accounts.5b00301 · Cited by 297

Flagged first, then by citations

Show all 74 references

2 of the 74 references couldn’t be matched to a known paper.

Research works printed but not linked: 3

Albrecht-Gary A-M, Crumbliss AL. 1999 Siderophore mediated microbial iron bioavailability: A paradigm for specific metal ion transport. In: Scientific Bridges for 2000 and Beyond. Paris: Académie des Sciences, Editions TEC & DOC; pp. 73-89.
Dhungana S, Crumbliss AL. 2001 Microbial iron transport via a siderophore shuttle: A membrane ion transport paradigm. ChemTracts-Inorg Chem 14, 258-265.
Novicova NM, Novikov VT. 1981 Kinetics of complex formation by iron(III) with thyrone and 2,7-dichlorochromotropic acid. Russ J Inorg Chem 26, 759-760.

Sorted by citations

Items 101–200 of 568

Iron acquisition in maize (Zea mays L.) using Pseudomonas siderophore
Sah, S., Singh, N., & Singh, R. (2017) · 3 Biotech · doi:10.1007/s13205-017-0772-z · Cited by 84
Genome Insights of the Plant-Growth Promoting Bacterium Cronobacter muytjensii JZ38 With Volatile-Mediated Antagonistic Activity Against Phytophthora infestans
Eida, A. A., Bougouffa, S., L’Haridon, F., Alam, I. S., Weisskopf, L., Bajić, V. B., Saad, M. M., & Hirt, H. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00369 · Cited by 83
Metallomics: lessons for metalliferous soil remediation
Haferburg, G., & Kothe, E. (2010) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-010-2695-z · Cited by 83
Iron metabolism in aerobes: Managing ferric iron hydrolysis and ferrous iron autoxidation
Kosman, D. J. (2012) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2012.06.030 · Cited by 82
Possible mechanisms for the equilibrium of ACC and role of ACC deaminase-producing bacteria
Moon, Y. S., & Ali, S. (2022) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-022-11772-x · Cited by 80
Marine Biogeochemistry of Iron
Ussher, S. J., Achterberg, E. P., & Worsfold, P. J. (2004) · Environmental Chemistry · doi:10.1071/en04053 · Cited by 80
Physiological and Proteomic Analysis of Escherichia coli Iron-Limited Chemostat Growth
Folsom, J. P., Parker, A. E., & Carlson, R. P. (2014) · Journal of Bacteriology · doi:10.1128/jb.01606-14 · Cited by 80
Marine amphiphilic siderophores: Marinobactin structure, uptake, and microbial partitioning
Martinez, J. S., & Butler, A. (2007) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2007.07.007 · Cited by 79
The redox hypothesis in siderophore-mediated iron uptake
Harrington, J. M., & Crumbliss, A. L. (2009) · BioMetals · doi:10.1007/s10534-009-9233-4 · Cited by 77
Self-citation
Quantum chemical study of the Fe(III)-desferrioxamine B siderophore complex—Electronic structure, vibrational frequencies, and equilibrium Fe-isotope fractionation
Domagal-Goldman, S. D., Paul, K. W., Sparks, D. L., & Kubicki, J. D. (2008) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2008.09.031 · Cited by 77
Cellular organization of siderophore biosynthesis in Pseudomonas aeruginosa: Evidence for siderosomes
Gasser, V., Guillon, L., Cunrath, O., & Schalk, I. J. (2015) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2015.01.017 · Cited by 77
Bypasses in intracellular glucose metabolism in iron‐limited Pseudomonas putida
Sasnow, S. S., Wei, H., & Aristilde, L. (2015) · MicrobiologyOpen · doi:10.1002/mbo3.287 · Cited by 77
Binding Properties of Pyochelin and Structurally Related Molecules to FptA of Pseudomonas aeruginosa
Mislin, G. L. A., Hoegy, F., Cobessi, D., Poole, K., Rognan, D., & Schalk, I. J. (2006) · Journal of Molecular Biology · doi:10.1016/j.jmb.2006.01.080 · Cited by 75
Bacterial Siderophores Promote Dissolution of UO2 under Reducing Conditions
Frazier, S. W., Kretzschmar, R., & Kraemer, S. M. (2005) · Environmental Science & Technology · doi:10.1021/es050270n · Cited by 75
Phytotoxin production in Aspergillus terreus is regulated by independent environmental signals
Gressler, M., Meyer, F., Heine, D., Hortschansky, P., Hertweck, C., & Brock, M. (2015) · eLife · doi:10.7554/elife.07861 · Cited by 73
A Comparative Study of Iron Uptake Rates and Mechanisms amongst Marine and Fresh Water Cyanobacteria: Prevalence of Reductive Iron Uptake
Lis, H., Kranzler, C. F., Keren, N., & Shaked, Y. (2015) · Life · doi:10.3390/life5010841 · Cited by 72
Siderophore‐promoted dissolution of smectite by fluorescent P seudomonas
Ferret, C., Sterckeman, T., Cornu, J., Gangloff, S. C., Schalk, I. J., & Geoffroy, V. A. (2014) · Environmental Microbiology Reports · doi:10.1111/1758-2229.12146 · Cited by 71
Ortho-Substituted Catechol Derivatives: The Effect of Intramolecular Hydrogen-Bonding Pathways on Chloride Anion Recognition
Winstanley, K. J., & Smith, D. K. (2007) · The Journal of Organic Chemistry · doi:10.1021/jo0623989 · Cited by 70
Bacterial Iron Uptake Pathways: Gates for the Import of Bactericide Compounds
Schalk, I. J., & Mislin, G. L. A. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b00554 · Cited by 70
π-Plasmon absorption of carbon nanotubes for the selective and sensitive detection of Fe 3+ ions
Cheung, W. K. L., Patel, M. A., Ma, Y., Chen, Y., Xie, Q., Lockard, J. V., Gao, Y., & He, H. (2016) · Chemical Science · doi:10.1039/c6sc00006a · Cited by 69
Dissolution of hausmannite (Mn3O4) in the presence of the trihydroxamate siderophore desferrioxamine B
Peña, J., Duckworth, O. W., Bargar, J., & Sposito, G. (2007) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2007.03.043 · Cited by 68
Pseudomonas putidaResponse to Cadmium: Changes in Membrane and Cytosolic Proteomes
Manara, A., DalCorso, G., Baliardini, C., Farinati, S., Cecconi, D., & Furini, A. (2012) · Journal of Proteome Research · doi:10.1021/pr300281f · Cited by 67
Iron bioavailability in the Southern Ocean
Hassler, C. S., Schoemann, V., Boyé, M., Tagliabue, A., Rozmarynowycz, M. J., & McKay, R. M. L. (2012) · Oceanography and Marine Biology/Oceanography and marine biology - an annual review · doi:10.1201/b12157-2 · Cited by 67
The exceptionally stable cobalt(III)–desferrioxamine B complex
Duckworth, O. W., Bargar, J., Jarzęcki, A. A., Oyerinde, O. F., Spiro, T. G., & Sposito, G. (2009) · Marine Chemistry · doi:10.1016/j.marchem.2009.01.003 · Cited by 66
Binding of Iron-free Siderophore, a Common Feature of Siderophore Outer Membrane Transporters of Escherichia coli and Pseudomonas aeruginosa
Hoegy, F., Celia, H., Mislin, G. L. A., Vincent, M., Gallay, J., & Schalk, I. J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m500776200 · Cited by 66
An overview of the biological metal uptake pathways in P seudomonas aeruginosa
Schalk, I. J., & Cunrath, O. (2016) · Environmental Microbiology · doi:10.1111/1462-2920.13525 · Cited by 65
Endophytic bacteria associated with endangered plant Ferula sinkiangensis K. M. Shen in an arid land: diversity and plant growth-promoting traits
Liu, Y., Guo, J., Li, L., Asem, M. D., Zhang, Y., Mohamad, O. A. A., Salam, N., & Li, W. (2017) · Journal of Arid Land · doi:10.1007/s40333-017-0015-5 · Cited by 65
Root‐induced soil deformation influences Fe, S and P: rhizosphere chemistry investigated using synchrotron XRF and XANES
van Veelen, A., Koebernick, N., Scotson, C. S., Fletcher, D. M., Huthwelker, T., Borca, C. N., Mosselmans, J. F. W., & Roose, T. (2019) · New Phytologist · doi:10.1111/nph.16242 · Cited by 65
EPR and Mössbauer Spectroscopy of Intact Mitochondria Isolated from Yah1p-DepletedSaccharomyces cerevisiae
Miao, R., Martinho, M., Morales, J. G., Kim, H., Ellis, E. A., Lill, R., Hendrich, M. P., Münck, E., & Lindahl, P. A. (2008) · Biochemistry · doi:10.1021/bi801047q · Cited by 62
Silicon Alleviates Iron Deficiency in Barley by Enhancing Expression of Strategy II Genes and Metal Redistribution
Nikolić, D. B., Nešić, S., Bosnić, D., Kostic, L., Nikolić, M., & Samardžić, J. T. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00416 · Cited by 61
Adsorption of rare earth elements by γ-Al2O3 and Pseudomonas fluorescens cells in the presence of desferrioxamine B: implication of siderophores for the Ce anomaly
Yoshida, T., Ozaki, T., Ohnuki, T., & Francis, A. J. (2004) · Chemical Geology · doi:10.1016/j.chemgeo.2004.08.046 · Cited by 60
Tolerance of Heavy Metal Toxicity Using PGPR Strains of Pseudomonas Species
Singh, S. K., Singh, P. P., Gupta, A., Singh, A. K., & Keshri, J. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-815879-1.00012-4 · Cited by 60
Siderophore-promoted dissolution of chromium from hydroxide minerals
Duckworth, O. W., Akafia, M. M., Andrews, M. Y., & Bargar, J. (2014) · Environmental Science Processes & Impacts · doi:10.1039/c3em00717k · Cited by 59
The Potent and Novel Thiosemicarbazone Chelators Di-2-pyridylketone-4,4-dimethyl-3-thiosemicarbazone and 2-Benzoylpyridine-4,4-dimethyl-3-thiosemicarbazone Affect Crucial Thiol Systems Required for Ribonucleotide Reductase Activity
Yu, Y., Rahmanto, Y. S., Hawkins, C. L., & Richardson, D. R. (2011) · Molecular Pharmacology · doi:10.1124/mol.111.071324 · Cited by 59
Syntheses of Siderophore–Drug Conjugates Using a Convergent Thiol–Maleimide System
Juárez-Hernández, R. E., Miller, P. A., & Miller, M. J. (2012) · ACS Medicinal Chemistry Letters · doi:10.1021/ml300150y · Cited by 58
Influence of light and temperature on the marine iron cycle: From theoretical to global modeling
Tagliabue, A., Bopp, L., Aumont, O., & Arrigo, K. R. (2009) · Global Biogeochemical Cycles · doi:10.1029/2008gb003214 · Cited by 58
Direct Evidence of Iron Uptake by the Gram-Positive Siderophore-Shuttle Mechanism without Iron Reduction
Fukushima, T., Allred, B. E., & Raymond, K. N. (2014) · ACS Chemical Biology · doi:10.1021/cb500319n · Cited by 57
Siderophore-mediated iron transport in Bacillus subtilis and Corynebacterium glutamicum
Dertz, E. A., Stintzi, A., & Raymond, K. N. (2006) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-006-0151-4 · Cited by 57
Legume Biofortification and the Role of Plant Growth-Promoting Bacteria in a Sustainable Agricultural Era
Roriz, M., Carvalho, S. M. P., Castro, P. M. L., & Vasconcelos, M. W. (2020) · Agronomy · doi:10.3390/agronomy10030435 · Cited by 56
Crystal structure of ferric-yersiniabactin, a virulence factor of Yersinia pestis
Miller, M. C., Parkin, S., Fetherston, J. D., Perry, R. D., & DeMoll, E. (2006) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2006.04.007 · Cited by 56
An Insight into Plant Growth-Promoting Rhizobacteria-Mediated Mitigation of Stresses in Plant
Borah, P., Gogoi, N., Asad, S. A., Rabha, A. J., & Farooq, M. (2022) · Journal of Plant Growth Regulation · doi:10.1007/s00344-022-10787-y · Cited by 55
Towards accounting for dissolved iron speciation in global ocean models
Tagliabue, A., & Völker, C. (2011) · Biogeosciences · doi:10.5194/bg-8-3025-2011 · Cited by 55
Multiple siderophores: bug or feature?
McRose, D. L., Seyedsayamdost, M. R., & Morel, F. M. M. (2018) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-018-1617-x · Cited by 54
Bisucaberin – A dihydroxamate siderophore isolated from Vibrio salmonicida, an important pathogen of farmed Atlantic salmon (Salmo salar)
Winkelmann, G., Schmid, D. G., NICHOLSON, G. J., Jung, G., & Colquhoun, D. J. (2002) · BioMetals · doi:10.1023/a:1015206419613 · Cited by 54
Complexation of oxoanions and cationic metals by the biscatecholate siderophore azotochelin
Bellenger, J., Arnaud‐Neu, F., Asfari, Z., Myneni, S. C. B., Stiefel, E. I., & Kraepiel, A. M. L. (2006) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-006-0194-6 · Cited by 54
BIOFORTIFICATION OF IRON IN CHICKPEA BY PLANT GROWTH PROMOTING RHIZOBACTERIA
Khalid, S., Asghar, H. N., Akhtar, M. J., Aslam, A., & Zahir, Z. A. (2015) · Pakistan Journal of Botany · Cited by 53
Iron
Marchetti, A., & Maldonado, M. T. (2016) · Springer eBooks · doi:10.1007/978-3-319-24945-2_11 · Cited by 53
Pyridine-2,6-bis(thiocarboxylic acid) Produced by Pseudomonas stutzeri KC Reduces Chromium(VI) and Precipitates Mercury, Cadmium, Lead and Arsenic
Zawadzka, A. M., Crawford, R. L., & Paszczynski, A. J. (2006) · BioMetals · doi:10.1007/s10534-006-9022-2 · Cited by 53
The Schizosaccharomyces pombe Corepressor Tup11 Interacts with the Iron-responsive Transcription Factor Fep1
Znaidi, S., Pelletier, B., Mukai, Y., & Labbé, S. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m312787200 · Cited by 52
Pathway to industrial application of heterotrophic organisms in critical metals recycling from e-waste
Golzar-Ahmadi, M., Bahaloo-Horeh, N., Pourhossein, F., Norouzi, F., Schönberger, N., Hintersatz, C., Chakankar, M., Holuszko, M., & Kaksonen, A. H. (2024) · Biotechnology Advances · doi:10.1016/j.biotechadv.2024.108438 · Cited by 51
FbpA — A bacterial transferrin with more to offer
Siburt, C. J. P., Mietzner, T. A., & Crumbliss, A. L. (2011) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2011.09.001 · Cited by 51
Self-citation
Synthesis, delivery and regulation of eukaryotic heme and Fe–S cluster cofactors
Barupala, D., Dzul, S. P., Riggs-Gelasco, P. J., & Stemmler, T. L. (2016) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2016.01.010 · Cited by 51
A Key Role for the Periplasmic PfeE Esterase in Iron Acquisition via the Siderophore Enterobactin in Pseudomonas aeruginosa
Perraud, Q., Moynié, L., Gasser, V., Munier, M., Godet, J., Hoegy, F., Mély, Y., Mislin, G. L. A., Naismith, J. H., & Schalk, I. J. (2018) · ACS Chemical Biology · doi:10.1021/acschembio.8b00543 · Cited by 51
Iron Chelation Properties of an Extracellular Siderophore Exochelin MN
Dhungana, S., Miller, M. J., Dong, L., Ratledge, C., & Crumbliss, A. L. (2003) · Journal of the American Chemical Society · doi:10.1021/ja029578u · Cited by 50
Self-citation
Synchrotron-based X-ray fluorescence microscopy enables multiscale spatial visualization of ions involved in fungal lignocellulose deconstruction
Kirker, G. T., Zelinka, S., Gleber, S.-C., Vine, D. J., Finney, L. A., Chen, S., Hong, Y. P., Uyarte, O., Vogt, S., Jellison, J., et al. (2017) · Scientific Reports · doi:10.1038/srep41798 · Cited by 50
Function of Siderophores in the Plant Rhizosphere
Pinton, R., Varanini, Z., & Nannipieri, P. (2007) · CRC Press eBooks · doi:10.1201/9781420005585-12 · Cited by 50
Nocardimicins A, B, C, D, E, and F, Siderophores with Muscarinic M3 Receptor Inhibiting Activity from Nocardia sp. TP-A0674
Ikeda, Y., Nonaka, H., FURUMAI, T., Onaka, H., & Igarashi, Y. (2005) · Journal of Natural Products · doi:10.1021/np050091j · Cited by 49
Dissolved iron(II) ligands in river and estuarine water
Hopwood, M. J., Statham, P. J., Skrabal, S. A., & Willey, J. D. (2014) · Marine Chemistry · doi:10.1016/j.marchem.2014.11.004 · Cited by 49
A Novel Iron-Chelating Derivative of the Neuroprotective Peptide NAPVSIPQ Shows Superior Antioxidant and Antineurodegenerative Capabilities
Blat, D., Weiner, L. M., Youdim, M. B. H., & Fridkin, M. (2007) · Journal of Medicinal Chemistry · doi:10.1021/jm070800l · Cited by 49
Fe(III) Oxide Reduction by a Gram-positive Thermophile: Physiological Mechanisms for Dissimilatory Reduction of Poorly Crystalline Fe(III) Oxide by a Thermophilic Gram-positive BacteriumCarboxydothermus ferrireducens
Gavrilov, S. N., Lloyd, J. R., Kostrikina, N. A., & Slobodkin, A. I. (2012) · Geomicrobiology Journal · doi:10.1080/01490451.2011.635755 · Cited by 49
Iron acquisition and regulation systems in Streptococcus species
Ge, R., & Sun, X. (2014) · Metallomics · doi:10.1039/c4mt00011k · Cited by 48
Iron(III) Coordination Properties of a Pyoverdin Siderophore Produced by Pseudomonas putida ATCC 33015
Boukhalfa, H., Reilly, S. D., Michalczyk, R., Iyer, S., & Neu, M. P. (2006) · Inorganic Chemistry · doi:10.1021/ic060196p · Cited by 48
Self-citation
Bacterial Iron Transport: Coordination Properties of Azotobactin, the Highly Fluorescent Siderophore ofAzotobacter vinelandii
Palanché, T., Blanc, S. P.-L., Hennard, C., Abdallah, M. A., & Albrecht‐Gary, A. (2003) · Inorganic Chemistry · doi:10.1021/ic034862n · Cited by 48
Iron Availability and Homeostasis in Plants: A Review of Responses, Adaptive Mechanisms, and Signaling
Kermeur, N., Pédrot, M., & Cabello‐Hurtado, F. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3044-0_3 · Cited by 47
Biofilm-forming microorganisms in the rhizosphere to improve plant growth: Coping with abiotic stress and environmental pollution
Brokate, O., Papenbrock, J., & Turcios, A. E. (2024) · Applied Soil Ecology · doi:10.1016/j.apsoil.2024.105591 · Cited by 47
A zonal picture of the water column distribution of dissolved iron(II) during the U.S. GEOTRACES North Atlantic transect cruise (GEOTRACES GA03)
Sedwick, P. N., Sohst, B. M., Ussher, S. J., & Bowie, A. R. (2014) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2014.11.004 · Cited by 47
Plant–microbe interactions in plants and stress tolerance
Etesami, H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818204-8.00018-7 · Cited by 47
Enterococcus faecalis Antagonizes Pseudomonas aeruginosa Growth in Mixed-Species Interactions
Tan, C. A. Z., Lam, L. N., Biuković, G., Soh, E. Y., Toh, X. W., Lemos, J. A. C., & Kline, K. A. (2022) · Journal of Bacteriology · doi:10.1128/jb.00615-21 · Cited by 47
Direct Protocol for Ambient Mass Spectrometry Imaging on Agar Culture
Angolini, C. F. F., Vendramini, P. H., Araújo, F. D. D. S., Araújo, W. L., Augusti, R., Eberlin, M. N., & Oliveira, L. G. D. (2015) · Analytical Chemistry · doi:10.1021/acs.analchem.5b01538 · Cited by 47
Hierarchical routing in carbon metabolism favors iron-scavenging strategy in iron-deficient soil Pseudomonas species
Mendonca, C. M., Yoshitake, S., Wei, H., Werner, A., Sasnow, S. S., Thannhauser, T. W., & Aristilde, L. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2016380117 · Cited by 46
Management of Plant Diseases by PGPR-Mediated Induced Resistance with Special Reference to Tea and Rice Crops
Suryadi, Y., Susilowati, D. N., & Fauziah, F. (2019) · Microorganisms for sustainability · doi:10.1007/978-981-13-6986-5_4 · Cited by 46
Plant Growth-Promoting Rhizobacteria (PGPRs): Functions and Benefits
Singh, D., Ghosh, P., Kumar, J., & Kumar, A. (2019) · Springer eBooks · doi:10.1007/978-981-13-8383-0_7 · Cited by 46
Towards accounting for dissolved iron speciation in global ocean modelsPreprint
Tagliabue, A., & Völker, C. (2011) · doi:10.5194/bgd-8-2775-2011 · Cited by 46
Alleviation of Salinity Induced Oxidative Stress in Chenopodium quinoa by Fe Biofortification and Biochar—Endophyte Interaction
Naveed, M., Ramzan, N., Mustafa, A., Samad, A., Niamat, B., Yaseen, M., Ahmad, Z., Hasanuzzaman, M., Sun, N., Shi, W., et al. (2020) · Agronomy · doi:10.3390/agronomy10020168 · Cited by 45
Purification and Structural Characterization of Siderophore (Corynebactin) from Corynebacterium diphtheriae
Zajdowicz, S. L. W., Haller, J. C., Krafft, A. E., Hunsucker, S. W., Mant, C. T., Duncan, M. W., Hodges, R. S., Jones, D. N. M., & Holmes, R. K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034591 · Cited by 45
Function of Siderophores in the Plant Rhizosphere
Crowley, D. E., & Kraemer, S. M. (2007) · Books in soils, plants, and the environment · doi:10.1201/9781420005585.ch7 · Cited by 45
Complexation modulated redox behavior of transition metal systems (review)
Rizvi, M. A. (2015) · Russian Journal of General Chemistry · doi:10.1134/s1070363215040337 · Cited by 44
Reoxidation of Biogenic Reduced Uranium: A Challenge Toward Bioremediation
Singh, G., Şengör, S. S., Bhalla, A., Kumar, S., De, J., Stewart, B. D., Spycher, N. F., Ginn, T. M., Peyton, B., & Sani, R. K. (2013) · Critical Reviews in Environmental Science and Technology · doi:10.1080/10643389.2012.728522 · Cited by 44
The origin, composition, and reactivity of dissolved iron(III) complexes in coastal organic- and iron-rich sediments
Beckler, J., Jones, M. E., & Taillefert, M. (2015) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2014.12.017 · Cited by 42
Ternary Complex Formation Facilitates a Redox Mechanism for Iron Release from a Siderophore
Mies, K. A., Wirgau, J. I., & Crumbliss, A. L. (2006) · BioMetals · doi:10.1007/s10534-005-4342-1 · Cited by 42
Self-citation
Microbial ligand coordination: Consideration of biological significance
Springer, S. D., & Butler, A. (2015) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2015.03.013 · Cited by 40
Bacterial resistance to lead: Chemical basis and environmental relevance
Nong, Q., Yuan, K., Li, Z., Chen, P., Huang, Y., Hu, L., Jiang, J., Luan, T., & Chen, B. (2019) · Journal of Environmental Sciences · doi:10.1016/j.jes.2019.04.022 · Cited by 40
Desferrioxamine-B adsorption to and iron dissolution from palygorskite and sepiolite
Shirvani, M., & Nourbakhsh, F. (2010) · Applied Clay Science · doi:10.1016/j.clay.2010.01.012 · Cited by 40
Radionuclide Geomicrobiology of the Deep Biosphere
Anderson, C. R., Johnsson, A., Moll, H., & Pedersen, K. (2011) · Geomicrobiology Journal · doi:10.1080/01490451.2010.507644 · Cited by 40
Siderophore mediated attenuation of cadmium toxicity by paddy field cyanobacterium Anabaena oryzae
Singh, A., Kaushik, M. S., Srivastava, M., Tiwari, D. N., & Mishra, A. K. (2016) · Algal Research · doi:10.1016/j.algal.2016.02.030 · Cited by 40
Microbial siderophores as molecular shuttles for metal cations: sources, sinks and application perspectives
Karuppiah, V., Murugan, S., Sivasakthivelan, P., & Thangavel, K. (2023) · Archives of Microbiology · doi:10.1007/s00203-023-03644-3 · Cited by 39
Integrating microbial siderophores into concepts of plant iron nutrition
Gu, S., Wang, N., Zheng, Y., Wang, T., Shen, Q., Zhang, F. S., Kümmerli, R., Wei, Z., & Zuo, Y. (2025) · Nature Plants · doi:10.1038/s41477-025-02171-x · Cited by 39
Structure–function relationships in the bifunctional ferrisiderophore FpvA receptor from Pseudomonas aeruginosa
Schalk, I. J., Lamont, I. L., & Cobessi, D. (2009) · BioMetals · doi:10.1007/s10534-008-9203-2 · Cited by 39
The Importance of Microbial Inoculants in a Climate-Changing Agriculture in Eastern Mediterranean Region
Kavadia, A., Omirou, M., Fasoula, D. A., & Ioannides, I. M. (2020) · Atmosphere · doi:10.3390/atmos11101136 · Cited by 39
Low Concentrations of Surfactants Enhance Siderophore-Promoted Dissolution of Goethite
Carrasco, N., Kretzschmar, R., Pesch, M.-L., & Kraemer, S. M. (2007) · Environmental Science & Technology · doi:10.1021/es062897r · Cited by 39
Structures of Streptococcus pneumoniae PiaA and Its Complex with Ferrichrome Reveal Insights into the Substrate Binding and Release of High Affinity Iron Transporters
Wang, C., Li, Q., Jiang, Y., Zhou, C., & Chen, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071451 · Cited by 39
Thermo-FTIR Spectroscopic Study of the Siderophore Ferrioxamine B: Spectral Analysis and Stereochemical Implications of Iron Chelation, pH, and Temperature
Siebner, H., Yariv, S., Lapides, Y., Hadar, Y., & Chen, Y. (2005) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf048359k · Cited by 39
Plant growth–promoting bacteria and their role in environmental management
Singh, D. K., Singh, S. K., Singh, V. K., Gupta, A., Aamir, M., & Kumar, A. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-818095-2.00008-4 · Cited by 38
Iron biofortification in cereal crops: Recent progress and prospects
Zulfiqar, U., Ayub, A., Hussain, S., Ahmad, M., Rehman, A., Ishfaq, M., Ali, M. F., Shabaan, M., & Yong, J. W. H. (2024) · Food and Energy Security · doi:10.1002/fes3.547 · Cited by 38
Soil solid-phase organic matter-mediated microbial reduction of iron minerals increases with land use change sequence from fallow to paddy fields
Tan, W., Yuan, Y., Zhao, X., Dang, Q., Yuan, Y., Li, R., Cui, D., & Xi, B. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.04.288 · Cited by 38
Evidence for regulation of Fe(II) oxidation by organic complexing ligands in the Eastern Subarctic Pacific
Roy, E. G., & Wells, M. L. (2011) · Marine Chemistry · doi:10.1016/j.marchem.2011.08.006 · Cited by 38
Tetroazolemycins A and B, Two New Oxazole-Thiazole Siderophores from Deep-Sea Streptomyces olivaceus FXJ8.012
Liu, N., Shang, F., Xi, L., & Huang, Y. (2013) · Marine Drugs · doi:10.3390/md11051524 · Cited by 38
Membrane Dynamics of the Amphiphilic Siderophore, Acinetoferrin
Luo, M., Fadeev, E. A., & Groves, J. T. (2005) · Journal of the American Chemical Society · doi:10.1021/ja044230f · Cited by 38
Regulatory and pathogenic mechanisms in response to iron deficiency and excess in fungi
Pijuan, J., Moreno, D. F., Yahya, G., Moisa, M., Ul Haq, I., Krukiewicz, K., Mosbah, R., Metwally, K., & Cavalu, S. (2023) · Microbial Biotechnology · doi:10.1111/1751-7915.14346 · Cited by 37
The lime–silicate question
Bothe, H. (2015) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2015.07.004 · Cited by 37

Authors: Boukhalfa, H., & Crumbliss, A. L.
Affiliations: Duke University (US)
Corresponding author: Crumbliss, Alvin L.
ORCID: Boukhalfa, Hakim
Crumbliss, Alvin L.
Venue: Biometals
Publisher: Springer Science and Business Media LLC
Published: 2002-12
Volume: 15
Issue: 4
Pages: 325-339
ISSN: 0966-0844 (ISSN-L)
1572-8773
DOI: 10.1023/a:1020218608266
OpenAlex: W1657518708
Cited by: 547
References: 74
Citations by year: 2026: 7 · 2025: 14 · 2024: 21 · 2023: 27 · 2022: 22 · 2021: 24 · 2020: 32 · 2019: 27 · 2018: 25 · 2017: 34 · 2016: 26 · 2015: 28 · 2014: 32 · 2013: 18 · 2012: 27
FWCI: 2.35
Type: journal article
Language: en
Open access: closed
Licence: www.springernature.com/gp/researchers/text-and-data-mining (tdm)
www.springernature.com/gp/researchers/text-and-data-mining (vor)
Locations: BioMetals (publishedVersion)
PubMed (publishedVersion)
Funders: National Science Foundation
Topics: Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
Physical Sciences › Chemistry › Inorganic Chemistry › Inorganic and Organometallic Chemistry
Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
Keywords: siderophores, iron transport, iron acquisition, coordination chemistry, bioavailability, thermodynamics, kinetics, metal complexes
MeSH terms: Animals, Deferoxamine, Ferric Compounds, Humans, Hydrogen-Ion Concentration, Iron, Kinetics, Ligands, Oxidation-Reduction, Peptides, Cyclic, Solubility, Siderophores

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Chemical aspects of siderophore mediated iron transport

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks