Chemical aspects of siderophore mediated iron transport

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×

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

Two transcription factors are necessary for iron homeostasis in a salt-dwelling archaeon

Schmid, A., Pan, M., Sharma, K., & Baliga, N. S. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq1211 · Cited by 37

Impact of a Transposon Insertion in phzF2 on the Specialized Metabolite Production and Interkingdom Interactions of Pseudomonas aeruginosa

Phelan, V. V., Moree, W. J., Aguilar, J., Cornett, D. S., Koumoutsi, A., Noble, S. M., Pogliano, K., Guerrero, C. A., & Dorrestein, P. C. (2014) · Journal of Bacteriology · doi:10.1128/jb.01258-13 · Cited by 37

Iron sequestration in brown-rot fungi by oxalate and the production of reactive oxygen species (ROS)

Zhu, Y. C., Zhuang, L., Goodell, B. S., Cao, J., & Mahaney, J. E. (2016) · International Biodeterioration & Biodegradation · doi:10.1016/j.ibiod.2016.01.023 · Cited by 37

Photodissolution of lepidocrocite (γ-FeOOH) in the presence of desferrioxamine B and aerobactin

Borer, P., Kraemer, S. M., Sulzberger, B., Hug, S. J., & Kretzschmar, R. (2009) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2009.05.049 · Cited by 36

Bioprospecting of endophytic bacteria from the Indian Himalayas and their role in plant growth promotion of maize (Zea mays L.)

Rana, K. L., Kour, D., Kaur, T., Rubee, D., Ashok, Y., & Nath, Y. A. (2021) · Journal of Applied Biology & Biotechnology · doi:10.7324/jabb.2021.9306 · Cited by 36

Significance of Soil Siderophore-Producing Bacteria in Evaluation and Elevation of Crop Yield

Zhang, S., Deng, Z., Borham, A., Ma, Y., Wang, Y., Hu, J., Wang, J., & Bohu, T. (2023) · Horticulturae · doi:10.3390/horticulturae9030370 · Cited by 36

Siderophore-promoted dissolution of cobalt from hydroxide minerals

Bi, Y., Hesterberg, D. L., & Duckworth, O. W. (2010) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2010.02.028 · Cited by 37

Directing the Biosynthesis of Putrebactin or Desferrioxamine B in Shewanella putrefaciens through the Upstream Inhibition of Ornithine Decarboxylase

Soe, C. Z., Pakchung, A. A. H., & Codd, R. (2012) · Chemistry & Biodiversity · doi:10.1002/cbdv.201200014 · Cited by 36

Role of Siderophores in Crop Improvement

Desai, A. J., & Archana, G. (2011) · Springer eBooks · doi:10.1007/978-3-642-21061-7_6 · Cited by 36

War-Fe-re: iron at the core of fungal virulence and host immunity

Nevitt, T. (2011) · BioMetals · doi:10.1007/s10534-011-9431-8 · Cited by 35

Siderophore-Producing Spinacia Oleracea Bacterial Endophytes Enhance Nutrient Status and Vegetative Growth Under Iron-Deficit Conditions

Misra, S., Semwal, P., Pandey, D. D., Mishra, S. K., & Chauhan, P. S. (2023) · Journal of Plant Growth Regulation · doi:10.1007/s00344-023-11185-8 · Cited by 35

Metallophore mapping in complex matrices by metal isotope coded profiling of organic ligands

Deicke, M., Mohr, J. F., Bellenger, J., & Wichard, T. (2014) · The Analyst · doi:10.1039/c4an01461h · Cited by 35

Optimization of Culture Medium to Increase the Production of Desferrioxamine B (Desferal) in Streptomyces pilosus

Chiani, M., Akbarzadeh, A., Farhangi, A. A., Mazinani, M., Saffari, Z., Emadzadeh, K., & Mehrabi, M. R. (2010) · Pakistan Journal of Biological Sciences · doi:10.3923/pjbs.2010.546.550 · Cited by 35

Simultaneous biosynthesis of putrebactin, avaroferrin and bisucaberin by Shewanella putrefaciens and characterisation of complexes with iron(III), molybdenum(VI) or chromium(V)

Soe, C. Z., Telfer, T. J., Levina, A., Lay, P. A., & Codd, R. (2015) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2015.12.008 · Cited by 35

Cultivation dependent formation of siderophores by Gordonia rubripertincta CWB2

Schwabe, R., Senges, C. H. R., Bandow, J. E., Heine, T., Lehmann, H., Wiche, O., Schlömann, M., Levicán, G. J., & Tischler, D. (2020) · Microbiological Research · doi:10.1016/j.micres.2020.126481 · Cited by 35

Combined Effects of Fe(III)-Bearing Nontronite and Organic Ligands on Biogenic U(IV) Oxidation

Xia, Q., Jin, Q., Chen, Y., Zhang, L., Li, X., He, S., Guo, D., Liu, J., & Dong, H. (2022) · Environmental Science & Technology · doi:10.1021/acs.est.1c04946 · Cited by 35

Purification and characterization of rhodobactin: a mixed ligand siderophore from Rhodococcus rhodochrous strain OFS

Dhungana, S., Michalczyk, R., Boukhalfa, H., Lack, J. G., Koppisch, A. T., Fairlee, J. M., Johnson, M. T., Ruggiero, C. E., John, S. G., Cox, M. M., et al. (2007) · BioMetals · doi:10.1007/s10534-006-9079-y · Cited by 35

The effect of desferrioxamine B, enterobactin, oxalic acid, and Na-alginate on the dissolution of uranyl-treatedgoethite at pH 6 and 25 °C

Wolff-Boenisch, D., & Traina, S. J. (2007) · Chemical Geology · doi:10.1016/j.chemgeo.2007.06.013 · Cited by 35

Tren-Based Analogues of Bacillibactin: Structure and Stability1

Dertz, E. A., Xu, J., & Raymond, K. N. (2006) · Inorganic Chemistry · doi:10.1021/ic060321x · Cited by 35

Sensitive detection of pyoverdine with an electrochemical sensor based on electrochemically generated graphene functionalized with gold nanoparticles

Gandouzi, I., Tertiş, M., Cernat, A., Bakhrouf, A., Coroş, M., Pruneanu, S. M., & Cristea, C. (2017) · Bioelectrochemistry · doi:10.1016/j.bioelechem.2017.11.014 · Cited by 35

Synthesis, Structure, and Molecular Dynamics of Gallium Complexes of Schizokinen and the Amphiphilic Siderophore Acinetoferrin

Fadeev, E. A., Luo, M., & Groves, J. T. (2004) · Journal of the American Chemical Society · doi:10.1021/ja048145j · Cited by 35

Isolation of cadmium-resistance and siderophore-producing endophytic bacteria and their potential use for soil cadmium remediation

Li, Y., Wei, S., Chen, X., Dong, Y., Zeng, M., Yan, C., Hou, L., & Jiao, R. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e17661 · Cited by 34

Microbially Enhanced Phytoextraction of Heavy-Metal Fly-Ash Amended Soil

Tiwari, S., Singh, S. N., & Garg, S. K. (2013) · Communications in Soil Science and Plant Analysis · doi:10.1080/00103624.2013.832287 · Cited by 34

Unsaturated Macrocyclic Dihydroxamic Acid Siderophores Produced byShewanella putrefaciensUsing Precursor-Directed Biosynthesis

Soe, C. Z., & Codd, R. (2014) · ACS Chemical Biology · doi:10.1021/cb400901j · Cited by 34

7-Hydroxytropolone produced and utilized as an iron-scavenger by Pseudomonas donghuensis

Jiang, Z., Chen, M., Yu, X., & Xie, Z. (2016) · BioMetals · doi:10.1007/s10534-016-9954-0 · Cited by 34

Collision‐induced dissociation of three groups of hydroxamate siderophores: ferrioxamines, ferrichromes and coprogens/fusigens

Mawji, E., Gledhill, M., Worsfold, P. J., & Achterberg, E. P. (2008) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.3604 · Cited by 34

Fe-Cycle Bacteria from Industrial Clays Mined in Georgia, USA

Shelobolina, E. S., Pickering, S. M., & Lovley, D. R. (2005) · Clays and Clay Minerals · doi:10.1346/ccmn.2005.0530604 · Cited by 34

Iron Chelation Equilibria, Redox, and Siderophore Activity of a Saccharide Platform Ferrichrome Analogue

Dhungana, S., Harrington, J. M., Gebhardt, P., Möllmann, U., & Crumbliss, A. L. (2007) · Inorganic Chemistry · doi:10.1021/ic070158l · Cited by 34

Making Soil More Accessible to Plants: The Case of Plant Growth Promoting Rhizobacteria

Turan, M., Kıtır, N., Alkaya, Ü., Günes, A., Tüfenkçi, Ş., Yıldırım, E., & Nıkerel, E. (2016) · InTech eBooks · doi:10.5772/64826 · Cited by 33

Iron-Dependent Remodeling of Fungal Metabolic Pathways Associated with Ferrichrome Biosynthesis

Mercier, A., & Labbé, S. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.00659-10 · Cited by 33

Desferrioxamine and desferrioxamine-caffeine as carriers of aluminum and gallium to microbes via the Trojan Horse Effect

Alvarado-Huayhuaz, J. A., Vitorino, H. A., Campos, O. S., Serrano, S. H. P., Kaneko, T. M., & Espósito, B. P. (2017) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2017.01.006 · Cited by 33

Adsorption of Enterobactin to Metal Oxides and the Role of Siderophores in Bacterial Adhesion to Metals

Upritchard, H. G., Yang, J., Bremer, P. J., Lamont, I. L., & McQuillan, A. J. (2011) · Langmuir · doi:10.1021/la202352j · Cited by 33

Harnessing Transition Metal Scaffolds for Targeted Antibacterial Therapy

Weng, C., Tan, Y. L. K., Koh, W. G., & Ang, W. H. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202310040 · Cited by 32

Iron acquisition strategies in pathogenic fungi

Takemura, K., Kolasinski, V., Poeta, M. D., de Sa, N. F. V., Garg, A., Ojima, I., Poeta, M. D., & de Sá, N. P. (2025) · mBio · doi:10.1128/mbio.01211-25 · Cited by 32

Fe(III) Coordination Properties of a New Saccharide-Based Exocyclic Trihydroxamate Analogue of Ferrichrome

Dhungana, S., Heggemann, S., Gebhardt, P., Möllmann, U., & Crumbliss, A. L. (2002) · Inorganic Chemistry · doi:10.1021/ic025647u · Cited by 32

Siderophores and the formation of cerium anomalies in anoxic environments

Kraemer, D., & Bau, M. (2022) · Geochemical Perspectives Letters · doi:10.7185/geochemlet.2227 · Cited by 31

Sulfate as a Synergistic Anion Facilitating Iron Binding by the Bacterial Transferrin FbpA: The Origins and Effects of Anion Promiscuity

Heymann, J. J., Weaver, K. D., Mietzner, T. A., & Crumbliss, A. L. (2007) · Journal of the American Chemical Society · doi:10.1021/ja0709268 · Cited by 31

Microbial Assisted Foliar Feeding of Micronutrients Enhance Growth, Yield and Biofortification of Wheat

Yaseen, M. (2018) · International Journal of Agriculture and Biology · doi:10.17957/ijab/15.0498 · Cited by 31

Synthesis and Iron Sequestration Equilibria of Novel Exocyclic 3-Hydroxy-2-pyridinone Donor Group Siderophore Mimics

Harrington, J. M., Chittamuru, S., Dhungana, S., Jacobs, H. K., Gopalan, A. S., & Crumbliss, A. L. (2010) · Inorganic Chemistry · doi:10.1021/ic902595c · Cited by 30

Isolation, screening, characterization, and optimization of bacteria isolated from calcareous soils for siderophore production

Kalyan, V. S. R. K., Meena, S., Karthikeyan, S., & Jawahar, D. (2022) · Archives of Microbiology · doi:10.1007/s00203-022-03322-w · Cited by 30

High cellular organization of pyoverdine biosynthesis in Pseudomonas aeruginosa : clustering of PvdA at the old cell pole

Guillon, L., Mecherki, M. E., Altenburger, S., Graumann, P. L., & Schalk, I. J. (2012) · Environmental Microbiology · doi:10.1111/j.1462-2920.2012.02741.x · Cited by 30

The determination of ferric iron in plants by HPLC using the microbial iron chelator desferrioxamine E

Fernández, V., & Winkelmann, G. (2005) · BioMetals · doi:10.1007/s10534-004-5773-9 · Cited by 30

Investigation of ascorbate-mediated iron release from ferric phytosiderophores in the presence of nicotianamine

Weber, G., von Wirén, N., & Hayen, H. (2008) · BioMetals · doi:10.1007/s10534-008-9137-8 · Cited by 30

Iron Coordination Properties of Gramibactin as Model for the New Class of Diazeniumdiolate Based Siderophores

Gama, S., Hermenau, R., Frontauria, M., Milea, D., Sammartano, S., Hertweck, C., & Plass, W. (2020) · Chemistry - A European Journal · doi:10.1002/chem.202003842 · Cited by 29

Uptake Mechanisms and Regulatory Responses to MECAM- and DOTAM-Based Artificial Siderophores and Their Antibiotic Conjugates in Pseudomonas aeruginosa

Fritsch, S., Gasser, V., Peukert, C., Pinkert, L., Kühn, L., Perraud, Q., Normant, V., Brönstrup, M., & Schalk, I. J. (2022) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.2c00049 · Cited by 29

Iron biofortification in wheat: Past, present, and future

Tanin, M. J., Saini, D. K., Kumar, P., Gudi, S., Sharma, H., Kaur, J. P., Abassy, O., Bromand, F., & Sharma, A. (2024) · Current Plant Biology · doi:10.1016/j.cpb.2024.100328 · Cited by 29

Ti(IV) and the Siderophore Desferrioxamine B: A Tight Complex Has Biological and Environmental Implications

Jones, K., Batchler, K. L., Zalouk, C., & Valentine, A. M. (2017) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.6b02399 · Cited by 29

Development of 1,3a,6a-triazapentalene-labeled enterobactin as a fluorescence quenching sensor of iron ion

Hayashi, T., Osawa, A., Watanabe, T., Murata, Y., Nakayama, A., & Namba, K. (2017) · Tetrahedron Letters · doi:10.1016/j.tetlet.2017.04.011 · Cited by 29

Iron supply to tobacco plants through foliar application of iron citrate and ferric dimerum acid

Fernández, V., Winkelmann, G., & Ebert, G. (2004) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2004.00405.x · Cited by 29

Kinetics and mechanism of iron release from the bacterial ferric binding protein nFbp: exogenous anion influence and comparison with mammalian transferrin

Boukhalfa, H., Anderson, D. S., Mietzner, T. A., & Crumbliss, A. L. (2003) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-003-0487-y · Cited by 29

Drawing with Iron on a Gel Containing a Supramolecular Siderophore

Xiao, S., Paukstelis, P. J., Ash, R. D., Zavalij, P. Y., & Davis, J. T. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201910872 · Cited by 28

DFT-based analysis of siderophore-metal ion interaction for efficient heavy metal remediation

Xu, Y., Li, N., Yan, X., & Zou, H.-X. (2023) · Environmental Science and Pollution Research · doi:10.1007/s11356-023-28854-6 · Cited by 28

The highly effective cadmium-resistant mechanism of Pseudomonas aeruginosa and the function of pyoverdine induced by cadmium

Mei, S., Bian, W.-P., Yang, A., Xu, P., Qian, X., Yang, L., Shi, X., & Niu, A. (2024) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2024.133876 · Cited by 28

Rapid identification of siderophores by combined thin‐layer chromatography/matrix‐assisted laser desorption/ionization mass spectrometry

Hayen, H., & Volmer, D. A. (2005) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.1837 · Cited by 28

Plant Growth–Promoting Microbes: A Boon for Sustainable Agriculture

Lalitha, S. (2017) · Springer eBooks · doi:10.1007/978-981-10-6647-4_8 · Cited by 28

Iron Chelation Properties of an Extracellular Siderophore Exochelin MS

Dhungana, S., Ratledge, C., & Crumbliss, A. L. (2004) · Inorganic Chemistry · doi:10.1021/ic049343e · Cited by 28

Impact of Vanadium Complexes Treatment on the Oxidative Stress Factors in Wistar Rats Plasma

Francik, R., Krośniak, M., Barlik, M., Kudła, A., Gryboś, R., & Librowski, T. (2011) · Bioinorganic Chemistry and Applications · doi:10.1155/2011/206316 · Cited by 28

A comparative study of the effect of desferrioxamine B, oxalic acid, and Na-alginate on the desorption of U(VI) from goethite at pH 6 and 25°C

Wolff-Boenisch, D., & Traina, S. J. (2006) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2006.06.1565 · Cited by 28

Syntheses of mycobactin analogs as potent and selective inhibitors of Mycobacterium tuberculosis

Juárez-Hernández, R. E., Franzblau, S. G., & Miller, M. J. (2012) · Organic & Biomolecular Chemistry · doi:10.1039/c2ob26077h · Cited by 28

Iron uptake pathway of Escherichia coli as an entry route for peptide nucleic acids conjugated with a siderophore mimic

Tsylents, U., Burmistrz, M., Wojciechowska, M., Stępień, J., Maj, P., & Trylska, J. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1331021 · Cited by 27

Electrochemistry of Iron(II/III)‐N,N'‐ethylene‐bis‐(o‐hydroxyphenylglycine) Complexes in Aqueous Solution Indicates Potential for Use in Redox Flow Batteries

Schröder, P., Obendorf, D., & Bechtold, T. (2019) · ChemElectroChem · doi:10.1002/celc.201900658 · Cited by 27

Role of Microorganisms as Biofertilizers

Mushtaq, Z., Faizan, S., & Hussain, A. (2020) · Springer eBooks · doi:10.1007/978-3-030-48771-3_6 · Cited by 27

KCa(H2O)2[FeIII(CN)6]⋅H2O Nanoparticles as an Antimicrobial Agent against Staphylococcus aureus

Wang, Z., Yu, B., Alamri, H. M., Yarabarla, S., Kim, M., & Huang, S. D. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201713177 · Cited by 27

Iron(III) Coordination Chemistry of Alterobactin A: A Siderophore from the Marine Bacterium Alteromonas luteoviolacea

Holt, P. D., Reid, R. R., Lewis, B. L., Luther, G. W., & Butler, A. (2005) · Inorganic Chemistry · doi:10.1021/ic0512072 · Cited by 27

Synthesis, cytotoxic activity and DNA-interaction studies of novel anthraquinone–thiosemicarbazones with tautomerizable methylene group

Marković, V. R., Janićijević, A., Stanojković, T., Kolundžija, B., Sladić, D. M., Vujčić, M. T., Janović, B. S., Joksović, L. G., Đjurdjević, P., Todorović, N. M., et al. (2013) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2013.03.071 · Cited by 27

The E. coli Siderophores Enterobactin and Salmochelin Form Six‐Coordinate Silicon Complexes at Physiological pH

Schmiederer, T., Rausch, S., Valdebenito, M., Mantri, Y., Mösker, E., Baramov, T., Stelmaszyk, K., Schmieder, P., Butz, D., Müller, S. I., et al. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201005792 · Cited by 27

Isolation, Structure Elucidation, and Iron-Binding Properties of Lystabactins, Siderophores Isolated from a Marine Pseudoalteromonas sp.

Zane, H. K., & Butler, A. (2013) · Journal of Natural Products · doi:10.1021/np3008655 · Cited by 27

Characterization of two siderophores produced by Bacillus megaterium: A preliminary investigation into their potential as therapeutic agents

Chuljerm, H., Deeudom, M., Fucharoen, S., Mazzacuva, F., Hider, R. C., Srichairatanakool, S., & Cilibrizzi, A. (2020) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2020.129670 · Cited by 26

Siderophore production by streptomycetes—stability and alteration of ferrihydroxamates in heavy metal-contaminated soil

Schütze, E., Ahmed, E., Voit, A., Klose, M., Greyer, M., Svatoš, A., Merten, D., Roth, M., Holmström, S., & Kothe, E. (2014) · Environmental Science and Pollution Research · doi:10.1007/s11356-014-3842-3 · Cited by 26

Interactions between iron availability, aluminium toxicity and fungal siderophores

Illmer, P., & Buttinger, R. (2006) · BioMetals · doi:10.1007/s10534-005-3496-1 · Cited by 26

Oxinobactin and Sulfoxinobactin, Abiotic Siderophore Analogues to Enterobactin Involving 8-Hydroxyquinoline Subunits: Thermodynamic and Structural Studies

d′Hardemare, A. D. M., Gellon, G., Philouze, C., & Serratrice, G. (2012) · Inorganic Chemistry · doi:10.1021/ic301081a · Cited by 26

Interactions in Soil-Microbe-Plant System: Adaptation to Stressed Agriculture

Shilev, S., Azaizeh, H., Vassilev, N. B., Georgiev, D., & Babrikova, I. (2019) · Springer eBooks · doi:10.1007/978-981-13-8391-5_6 · Cited by 26

Factors affecting the metal ion–hydroxamate interactions II: effect of the length of the connecting chain on the Fe(III), Mo(VI) and V(V) complexation of some new desferrioxamine B (DFB) model dihydroxamic acids

Farkas, E., Buglyó, P., Enyedy, É. A., & Santos, M. A. (2004) · Inorganica Chimica Acta · doi:10.1016/j.ica.2004.02.007 · Cited by 26

Metal-Dependent Self-Assembly of a Microbial Surfactant

Owen, T., Pynn, R., Hammouda, B., & Butler, A. (2007) · Langmuir · doi:10.1021/la700671p · Cited by 26

Ligand-Induced U Mobilization from Chemogenic Uraninite and Biogenic Noncrystalline U(IV) under Anoxic Conditions

Chardi, K. J., Satpathy, A., Schenkeveld, W. D. C., Kumar, N., Noël, V., Kraemer, S. M., & Giammar, D. E. (2022) · Environmental Science & Technology · doi:10.1021/acs.est.1c07919 · Cited by 25

Chelating Effect of Siderophore Desferrioxamine-B on Uranyl Biomineralization Mediated by Shewanella putrefaciens

Lü, X., Zhang, Y., Cheng, W., Liu, Y., Li, Q., Li, X., Dong, F., Li, J., & Nie, X. (2024) · Environmental Science & Technology · doi:10.1021/acs.est.3c05753 · Cited by 25

Synthesis of novel Iron(III) chelators based on triaza macrocycle backbone and 1-hydroxy-2(H)-pyridin-2-one coordinating groups and their evaluation as antimicrobial agents

Workman, D. G., Hunter, M., Dover, L. G., & Tétard, D. (2016) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2016.04.018 · Cited by 25

Microbial-Assisted Phytoremediation: A Convenient Use of Plant and Microbes to Clean Up Soils

Pinto, A. P., de Varennes, A., Dias, C. B., & Lopes, M. E. (2018) · Springer eBooks · doi:10.1007/978-3-319-99651-6_2 · Cited by 25

Towards the Development of Effective Antioxidants—The Molecular Structure and Properties—Part 2

Lewandowska, H., Świsłocka, R., Priebe, W., Lewandowski, W., & Orzechowska, S. (2026) · Molecules · doi:10.3390/molecules31040720 · Cited by 24

Fungus-promoted transformation of lanthanides during the biooxidation of divalent manganese

Yu, Q., Ohnuki, T., Tanaka, K., Kozai, N., Yamasaki, S., Sakamoto, F., & Tani, Y. (2015) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2015.11.004 · Cited by 24

Mechanism of Ferripyoverdine Uptake by Pseudomonas aeruginosa Outer Membrane Transporter FpvA: No Diffusion Channel Formed at Any Time during Ferrisiderophore Uptake

Nader, M., Journet, L., Meksem, A., Guillon, L., & Schalk, I. J. (2011) · Biochemistry · doi:10.1021/bi101821n · Cited by 24

Engineering siderophore production in Pseudomonas to improve asbestos weathering

Lemare, M., Puja, H., David, S. R., Mathieu, S., Ihiawakrim, D., Geoffroy, V. A., & Rigouin, C. (2022) · Microbial Biotechnology · doi:10.1111/1751-7915.14099 · Cited by 24

Structural and Functional Aspects of Metal Binding Sites in Natural and Designed Metalloproteins

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Kim, D., Duckworth, O. W., & Strathmann, T. J. (2009) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2009.12.020 · Cited by 24

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Moon, H., Park, J., & Tae, J. (2015) · The Chemical Record · doi:10.1002/tcr.201500226 · Cited by 24

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Zhu, Y. C., Mahaney, J. E., Jellison, J., Cao, J., Gressler, J., Hoffmeister, D., & Goodell, B. S. (2016) · Journal of Industrial Microbiology & Biotechnology · doi:10.1007/s10295-016-1889-5 · Cited by 24

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Guo, M., Gao, J., Yang, M., Liu, Y., Fu, J., Ma, R., Xiong, F., Zhang, T., Liu, X., Jin, Y. T., et al. (2025) · Applied Soil Ecology · doi:10.1016/j.apsoil.2025.106327 · Cited by 23

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Chincholkar, S. B., Chaudhari, B. L., & Rane, M. (2007) · Springer eBooks · doi:10.1007/978-3-540-71160-5_12 · Cited by 23

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Nguyen, A. T., & Oglesby, A. G. (2015) · BioMetals · doi:10.1007/s10534-015-9848-6 · Cited by 23

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Li, W., Si, J., Yu, T., & Li, X. (2016) · Journal of Arid Land · doi:10.1007/s40333-016-0045-4 · Cited by 23

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Gao, J., Xing, F., Bai, Y., & Zhu, S. (2014) · Dalton Transactions · doi:10.1039/c4dt00118d · Cited by 22

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Pesch, M.-L., Hoffmann, M., Christl, I., Kraemer, S. M., & Kretzschmar, R. (2012) · Geobiology · doi:10.1111/gbi.12010 · Cited by 22

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Raj, M., Kumar, R., Lal, K., Sirisha, L., Chaudhary, R., & Patel, S. K. (2020) · International Journal of Chemical Studies · doi:10.22271/chemi.2020.v8.i5b.10284 · Cited by 21

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Raymond, K. N., & Telford, J. R. (1995) · Springer eBooks · doi:10.1007/978-94-011-0255-1_3 · Cited by 9

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Guerinot, M. L. (1994) · Annual Review of Microbiology · doi:10.1146/annurev.mi.48.100194.003523 · Cited by 664

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