Bacterial siderophores in community and host interactions

The Tragedy of the Commons: The population problem has no technical solution; it requires a fundamental extension in morality.

Hardin, G. (1968) · Science · doi:10.1126/science.162.3859.1243 · Cited by 25,167

Biofilms: an emergent form of bacterial life

Flemming, H.-C., Wingender, J., Szewzyk, U., Steinberg, P., Rice, S. A., & Kjelleberg, S. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.94 · Cited by 5,979

On aims and methods of ethology

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Embracing the unknown: disentangling the complexities of the soil microbiome

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Induced systemic resistance by beneficial microbes

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Bacterial iron homeostasis

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Arms races between and within species

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Toxicity of heavy metals to microorganisms and microbial processes in agricultural soils: a review

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Social semantics: altruism, cooperation, mutualism, strong reciprocity and group selection.

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Siderophore-Based Iron Acquisition and Pathogen Control

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Ferruginous hemeprotein HhuH facilitates the cadmium adsorption and chromium reduction in Stenotrophomonas sp. SY1

Zhou, Z., Yu, H., Liu, J., Zhu, L., Wang, G., & Shi, K. (2024) · Applied and Environmental Microbiology · doi:10.1128/aem.02097-24 · Cited by 6

Discovery of Peptidic Siderophore Degradation by Screening Natural Product Profiles in Marine-Derived Bacterial Mono- and Cocultures

Monge-Loría, M., Zhong, W., Abrahamse, N. H., Hartter, S., & Garg, N. (2025) · Biochemistry · doi:10.1021/acs.biochem.4c00706 · Cited by 6

Natural and artificial siderophores: Iron-based applications and beyond

Lin, Z.-J., Fang, C.-Y., & Wang, T. A. (2025) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2025.102601 · Cited by 6

Unfolding the collective functional potential of a synergistic multispecies community through genotypic and phenotypic analyses

Ronin, D., Hansen, M. F., Flaig, M. L., Dueholm, M. S., Daugberg, A. O. H., Nesme, J., Kot, W., & Burmølle, M. (2025) · Biofilm · doi:10.1016/j.bioflm.2025.100290 · Cited by 6

Type VII secretion system deploys an active iron uptake pathway to enhance bacterial fitness and counteract host nutritional immunity

Luo, C., Hao, X., Wang, X. Q., Liu, M., Chen, S., Wu, C., Li, C., Chen, C., Yang, M., Xu, L., et al. (2025) · mBio · doi:10.1128/mbio.02419-25 · Cited by 6

Bacillus velezensis as a model for plant-associated beneficial bacilli

Borriss, R., Gao, X., & Fan, B. (2026) · Journal of Bacteriology · doi:10.1128/jb.00519-25 · Cited by 6

Bacterial Siderophore Production in Metal-Rich Environments: Underexplored Sources of Siderophores and Insights into Bioremediation

Knapp, M., & Giddings, L. (2026) · Journal of Natural Products · doi:10.1021/acs.jnatprod.5c01586 · Cited by 6

Rhizobacteria opportunistically boost colonization and impair plant fitness by degrading plant-derived coumarins under iron deficiency

Gu, Y., Pan, P., Yu, G., & Zhou, N. (2026) · Nature Communications · doi:10.1038/s41467-026-71037-3 · Cited by 6

Metagenomic Insights into the Adaptive Responses of the Microbiome of a Spent Engine Oil-Perturbed Agricultural Soil to Iron Stress

Salam, L. B. (2022) · Geomicrobiology Journal · doi:10.1080/01490451.2022.2158253 · Cited by 6

Overcoming the nutritional immunity by engineering iron-scavenging bacteria for cancer therapy

Huang, S., Lim, S.-K., Yu, Y., Pan, Y., Lien, W., Mou, C., Hu, C. J., & Mou, Y. (2023) · eLife · doi:10.7554/elife.90798 · Cited by 7

A critical role for iron and zinc homeostatic systems in the evolutionary adaptation of Escherichia coli to metal restriction

Paterson, J. R., Wadsworth, J. M., Hu, P., & Sharples, G. J. (2023) · Microbial Genomics · doi:10.1099/mgen.0.001153 · Cited by 6

Uncovering the Fungal Diversity and Biodeterioration Phenomenon on Archaeological Carvings of the Badami Cave Temples: A Microcosm Study

Agrawal, S., Khumlianlal, J., & Devi, S. I. (2023) · Life · doi:10.3390/life14010028 · Cited by 6

Genomics- and Transcriptomics-Guided Discovery of Clavatols from Arctic Fungi Penicillium sp. MYA5

Sun, Y., Hu, B., Yu, H., Zhou, J., Meng, X., Ning, Z., Ding, J., Cui, M., & Liu, X. (2024) · Marine Drugs · doi:10.3390/md22060236 · Cited by 6

Exploring microbial diversity and interactions for asbestos modifying properties

Wong, L. C., Rodenburg, U., Leite, R. R., Korthals, G. W., Pover, J., Koerten, H. K., Kuramae, E. E., & Bodelier, P. L. E. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.175577 · Cited by 6

Potential siderophore-dependent mutualism in the harmful dinoflagellate Alexandrium pacificum (Group IV) and bacterium Photobacterium sp. TY1-4 under iron-limited conditions

Jiang, Y., Shin, H. H., Park, B. S., & Li, Z. (2024) · Harmful Algae · doi:10.1016/j.hal.2024.102726 · Cited by 6

Blue mussel (Mytilus edulis L.) exposure to nylon microfibers leads to a shift in digestive gland microbiota

Stilo, G., Beltramo, C., Christoforou, E., Partipilo, T., Kormas, K. A., Spatharis, S., & Peletto, S. (2025) · Environmental Pollution · doi:10.1016/j.envpol.2025.125914 · Cited by 6

Design of Polymeric Thin Films to Direct Microbial Biofilm Growth, Virulence, and Metabolism

Franklin, T. J., Wu, Y., Lang, J., Li, S., & Yang, R. (2021) · Biomacromolecules · doi:10.1021/acs.biomac.1c00731 · Cited by 6

Toxicity of the iron siderophore mycobactin J in mouse macrophages: Evidence for a hypoxia response

McQueen, C. F., & Groves, J. T. (2021) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2021.111669 · Cited by 6

Antibiotic-active heterotrophic Firmicutes sheltered in seaweeds: can they add new dimensions to future antimicrobial agents?

Chakraborty, K., Varghese, C., Asharaf, S., & Chakraborty, R. D. (2022) · Archives of Microbiology · doi:10.1007/s00203-022-02784-2 · Cited by 6

High Affinity Iron Acquisition Systems Facilitate but Are Not Essential for Colonization of Chickens by Salmonella Enteritidis

Wellawa, D. H., Lam, P.-K. S., White, A. P., Gomis, S. M., Allan, B. J., & Köster, W. L. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.824052 · Cited by 6

Comparative metabolomic profiling of Cupriavidus necator B-4383 revealed production of cupriachelin siderophores, one with activity against Cryptococcus neoformans

Ahmed, M. M. A., Tripathi, S. K., & Boudreau, P. D. (2023) · Frontiers in Chemistry · doi:10.3389/fchem.2023.1256962 · Cited by 6

To cheat or not to cheat: cheatable and non-cheatable virulence factors in Pseudomonas aeruginosa

Guadarrama-Orozco, K. D., Pérez-González, C., Kota, K., Cocotl‐Yañez, M., Jiménez-Cortés, J. G., Díaz-Guerrero, M. Á., Hernández‐Garnica, M., Munson, J., Cadet, F., López-Jácome, L. E., et al. (2023) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiad128 · Cited by 6

Bacillus mexicanus sp. nov., a biological control bacterium isolated from the common bean (Phaseolus vulgaris L.) crop in Sinaloa, Mexico

Santos‐Villalobos, S. D. L., Pablos, C. M. F., Ruíz, V. V., & Parra-Cota, F. I. (2023) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijsem.0.006110 · Cited by 6

The Temperature-Dependent Expression of the High-Pathogenicity Island Encoding Piscibactin in Vibrionaceae Results From the Combined Effect of the AraC-Like Transcriptional Activator PbtA and Regulatory Factors From the Recipient Genome

Lages, M. A., Lemos, M. L., & Balado, M. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.748147 · Cited by 6

Microbial Inoculants in the Climate Change Scenario: An Overview

Singh, S., Pranaw, K., Prasanna, R., Kumar, P., & Poria, V. (2023) · Springer eBooks · doi:10.1007/978-981-99-2973-3_1 · Cited by 6

A Glance on the Role of Bacterial Siderophore from the Perspectives of Medical and Biotechnological Approaches

AlMatar, M., Albarri, O., Makky, E. A., Var, İ., & Köksal, F. (2020) · Current Drug Targets · doi:10.2174/1389450121666200621193018 · Cited by 10

Automated genome mining predicts structural diversity and taxonomic distribution of peptide metallophores across bacteriaPreprint

Reitz, Z. L., Pourmohsenin, B., Susman, M., Thomsen, E., Roth, D., Butler, A., Ziemert, N., & Medema, M. H. (2025) · eLife · doi:10.7554/elife.109154 · Cited by 6

ADAPTATION OF MICROORGANISMS TO HEAVY METALS

Mukhamatdyarov, S. R., Kuzina, E. V., Iskuzhina, M., & Korshunova, T. Y. (2023) · Izvestia Ufimskogo Nauchnogo Tsentra RAN · doi:10.31040/2222-8349-2023-0-4-31-43 · Cited by 5

Ion Mobility-Coupled Mass Spectrometry for Metallophore Detection

Bell, B. A., Anderson, J. M., Rajski, S. R., & Bugni, T. S. (2025) · Journal of Natural Products · doi:10.1021/acs.jnatprod.4c00911 · Cited by 5

Deciphering the Mechanism of Action of a Short, Synthetic Designer AMP Against Gram‐Negative Bacteria

Shadangi, S., Singh, A. P., & Rana, S. (2025) · Biopolymers · doi:10.1002/bip.70019 · Cited by 5

Biological control and mechanism characterization of endophytic Bacillus velezensis SJ22 against bulb rot of Fritillaria taipaiensis P. Y. Li

Wang, S., Chen, K., Wei, M., Zhou, L., Guo, J., Zhang, J., Cui, L., & Qiang, Y. (2025) · Biological Control · doi:10.1016/j.biocontrol.2025.105792 · Cited by 5

Integration of multi-modal measurements identifies critical mechanisms of tuberculosis drug action

Johnson, W. C., Alivisatos, A. P., Smith, T. C., Van, N., Soni, V., Wallach, J. B., Clark, N. A., Fitzgerald, T. A., Whiteley, J. J., Tan, S., et al. (2025) · Cell Systems · doi:10.1016/j.cels.2025.101348 · Cited by 5

Soil-dwelling Bacillus velezensis SS-38.4 efficiently colonizes sugar beet phyllosphere and controls phytopathogenic Pseudomonas syringae

Rosić, I., Nikolić, I., Šokić, M., Đorđević, S., Berić, T., Stanković, S., & Medić, O. (2025) · Phytopathology Research · doi:10.1186/s42483-025-00346-0 · Cited by 5

Multi-omics and molecular engineering insights into Pseudomonas spp.-mediated biocontrol of root-knot nematodes: An updated perspective

Shahid, M., & Shafi, Z. (2025) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2025.102972 · Cited by 5

Comparative Binding Studies of the Chelators Methylolanthanin and Rhodopetrobactin B to Lanthanides and Ferric Iron

Gutenthaler, S. M., Mertens, M., Phi, M. T., Weis, P., Drobot, B., Köhrer, A., Steudtner, R., Kärst, U., Martinez-Gomez, N. C., & Daumann, L. J. (2025) · ChemBioChem · doi:10.1002/cbic.202500312 · Cited by 6

Antagonistic Iron Competition Induced by Iron Chelators Heightens Cuproptosis in Both Tumors and Intratumoral Bacteria

Xie, Y., Wang, J., Han, Y., Zhu, G., Li, C., Sun, Q.-Q., & Li, C. (2025) · Advanced Materials · doi:10.1002/adma.202515904 · Cited by 5

Pseudopaline-mediated zinc uptake by Pseudomonas aeruginosa drives clinically relevant phenotypes and infection outcomes

Bosc, L., Sécher, T., Ball, G., Pennec, D. L., Tribout, M., Ba, M., Bai, Y., Ouerdane, L., Arnoux, P., Denis, Y., et al. (2026) · Infection and Immunity · doi:10.1128/iai.00453-25 · Cited by 5

Designing Tailored Bioinoculants for Sustainable Agrobiology in Multi-stressed Environments

Pajuelo, E., Carrasco, J. A., Flores-Duarte, N. J., Rodríguez-Llorente, I. D., Mesa‐Marín, J., Mateos‐Naranjo, E., Redondo‐Gómez, S., & Navarro‐Torre, S. (2023) · Microorganisms for sustainability · doi:10.1007/978-981-19-9570-5_16 · Cited by 5

Phenotypic and Genomic Characterization of Pseudomonas wuhanensis sp. nov., a Novel Species with Promising Features as a Potential Plant Growth-Promoting and Biocontrol Agent

Hou, J., Liao, K., Zhang, Y., Li, J., & Wei, H. (2024) · Microorganisms · doi:10.3390/microorganisms12050944 · Cited by 5

Plant growth-promoting potential of bacterial isolates from the rhizosphere of Deschampsia antarctica

Maslovska, O., Komplikevych, S., Danylo, I., Parnikoza, I., & Hnatush, S. О. (2024) · Ukrainian Antarctic Journal · doi:10.33275/1727-7485.1.2024.728 · Cited by 5

Synthesis of hydroxy-thiazoline substituted pyridine derivatives via [3 + 2] annulation of 1,4-dithiane-2,5-diol with cyanopyridine

Zhang, M., Chen, Y., Yan, X., Zhang, Y., & Ma, X. (2024) · Organic & Biomolecular Chemistry · doi:10.1039/d4ob01388c · Cited by 5

Proteomic analysis of natural photoheterotrophic mixed consortium for biohydrogen production under nongrowing conditions

Hernández-Guisao, R. E., González-García, R. A., McCubbin, T., Guerra-Blanco, P., Salgado, E., Aranda, J., Velasco, A., & Garcia-Peña, E. I. (2024) · Bioresource Technology · doi:10.1016/j.biortech.2024.132023 · Cited by 5

Microbial Iron Utilization Pathways in Constructed Wetlands: Analysis of Substrates Affecting Iron Transformation, Absorption, and Utilization

Zhao, X., Shi, Y., Yang, L., & Ho, S. (2025) · ACS ES&T Engineering · doi:10.1021/acsestengg.4c00448 · Cited by 5

Environmental transition navigates phenotype switching, affecting the virulence and multidrug-resistant profile of pathogenic Morganella morganii

Kumar, V., Das, B. K., Roy, S., Dhar, S., Bisai, K., Adhikari, A., Majumder, A., & Jana, A. K. (2025) · Microbial Pathogenesis · doi:10.1016/j.micpath.2025.107430 · Cited by 5

Decoding Lusichelins A–E: An In-Depth Look at the Metallophores of Lusitaniella coriacea LEGE 07167–Structure, Production, and Functionality

Sousa, M. L., Ferreira, L., Ferreira, D. I. R., Forero, A. M., Castelo‐Branco, R., Szemerédi, N., Spengler, G., Rodrı́guez, J., Jiménez, C., Leão, P. N., et al. (2025) · Journal of Natural Products · doi:10.1021/acs.jnatprod.5c00204 · Cited by 5

Iron and the Intestinal Microbiome

Li, H. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-92033-2_22 · Cited by 6

Bacterial Siderophores: Structure, Functions, and Role in the Pathogenesis of Infections

Kuznetsova, D. A., Александровна, Р. В., & On, P. (2022) · Problems of Particularly Dangerous Infections · doi:10.21055/0370-1069-2022-3-14-22 · Cited by 5

Proteins in Synthetic Biology with Agricultural and Environmental Applications

Mann, M. M., Vigil, T. N., Felton, S. M., Fahy, W. E., Kinkeade, M. A., Kartseva, V., Rowson, M.-J. C., Frost, A. J., & Berger, B. W. (2022) · SynBio · doi:10.3390/synbio1010006 · Cited by 5

The regulatory role of Fur-encoding SCLAV_3199 in iron homeostasis in Streptomyces clavuligerus

Abanoz-Seçgin, B., Otur, Ç., Okay, S., & Kurt‐Kızıldoğan, A. (2023) · Gene · doi:10.1016/j.gene.2023.147594 · Cited by 5

Thermostable homologues of the periplasmic siderophore-binding protein CeuE from Geobacillus stearothermophilus and Parageobacillus thermoglucosidasius

Blagova, E. V., Miller, A. H., Bennett, M., Booth, R. L., Dodson, E. J., Duhme‐Klair, A., & Wilson, K. S. (2023) · Acta Crystallographica Section D Structural Biology · doi:10.1107/s2059798323004473 · Cited by 5

Effects of deferoxamine on intrinsic colistin resistance of Proteus mirabilis

Erinmez, M., & Zer, Y. (2023) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2023.12158 · Cited by 5

The fitness benefit of pyoverdine cross‐feeding by Pseudomonas protegens Pf‐5

Smith, P. N., & Schuster, M. (2023) · Environmental Microbiology · doi:10.1111/1462-2920.16554 · Cited by 5

Functional Genomics of a Collection of Gammaproteobacteria Isolated from Antarctica

Giovannini, M., Vieri, W., Bosi, E., Riccardi, C., Giudice, A. L., Fani, R., Fondi, M., & Perrin, E. (2024) · Marine Drugs · doi:10.3390/md22060238 · Cited by 5

Zinc oxide biotransformation by mineral-dissolving rhizobacteria stimulated plant growth, physiochemical attributes, and mineral uptake in sunflower (Helianthus annuus L.)

Mumtaz, M. Z., Maqbool, H., Li, L., Ahmad, M., Raza, M. A., Saqib, M., Alsakkaf, W. A. A., & Ali, H. M. (2025) · Industrial Crops and Products · doi:10.1016/j.indcrop.2024.120000 · Cited by 5

Hybrid Genome Assembly for Predicting Functional Potential of a Novel Streptomyces Strain as Plant Biomass Valorisation Agent

Tikariha, H., Pavagadhi, S., Sevugan, M., Hong, M. P. C., & Swarup, S. (2021) · Indian Journal of Microbiology · doi:10.1007/s12088-021-00935-5 · Cited by 5

Plant-microbe features of Dendrobium fimbriatum (Orchidaceae) fungal community

Favre-Godal, Q., Schwob, P., Lecoultre, N., Hofstetter, V., Gourguillon, L., Riffault-Valois, L., Lordel-Madeleine, S., Gindro, K., & Choisy, P. (2021) · Symbiosis · doi:10.1007/s13199-021-00786-0 · Cited by 5

Interactions among Rhizosphere Microorganisms, Mechanisms and Potential Application in Phytoremediation

Feng, Y. (2022) · SHS Web of Conferences · doi:10.1051/shsconf/202214401003 · Cited by 5

Genome Sequence of Halomonas sp. Strain MS1, a Metallophore-Producing, Algal Growth-Promoting Marine Bacterium Isolated from the Green Seaweed Ulva mutabilis (Chlorophyta)

Morales‐Reyes, C. F., Ghaderiardakani, F., & Wichard, T. (2022) · Microbiology Resource Announcements · doi:10.1128/mra.00685-22 · Cited by 5

Frozen Clay Minerals as a Potential Source of Bioavailable Iron and Magnetite

Chung, H. Y., Jung, J., Yang, K., Kim, J., & Kim, K. (2023) · Environmental Science & Technology · doi:10.1021/acs.est.3c06144 · Cited by 5

A hypothesis about the influence of oxidative stress on amino acid protein composition during evolution

González-Tortuero, E., & Rodríguez-Rojas, A. (2023) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2023.1172785 · Cited by 5

Genome insights into the Bacillus paramycoides RZ3MS14: a multitrait plant growth-promoting rhizobacterium from Amazonian rainforest able to improve the sugarcane growth

Apaza-Castillo, G. A., Hosaka, G. K., Hayashibara, C. A. D. A., Fantine, R., Dourado, M. N., Rosa, M. S., Defant, H., & Quecine, M. C. (2025) · FEMS Microbiology Letters · doi:10.1093/femsle/fnaf123 · Cited by 5

Genomic insights into the molecular mechanisms of a Pseudomonas strain significant in its survival in Kongsfjorden, an Arctic fjord

Sinha, R. K., & Krishnan, K. P. (2021) · Molecular Genetics and Genomics · doi:10.1007/s00438-021-01788-9 · Cited by 5

Degradation of mirubactin to multiple siderophores with varying Fe( iii ) chelation properties

Pu, H., Jiang, T., Peng, D., Xia, J., Gao, J., Wang, Y., Yan, X., Huang, X., Duan, Y., & Huang, Y. P. (2022) · Organic & Biomolecular Chemistry · doi:10.1039/d2ob00942k · Cited by 5

Biostimulanten: soorten en werkingsmechanismen

Long, J. R. D., Streminska, M., & van der Salm, C. (2021) · doi:10.18174/551140 · Cited by 5

Benefit Transfer Loops Turn Cheating into a Scaffold for Microbial DiversityPreprint

Shao, J., Li, Y., Gu, S., Zhang, X., Wang, S., Liu, X., & Li, Z. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.21.568182 · Cited by 5

Improving rice drought tolerance through host-mediated microbiome selectionPreprint

Styer, A., Pettinga, D., Caddell, D. F., & Coleman‐Derr, D. (2024) · eLife · doi:10.7554/elife.97015.1 · Cited by 5

Screening of siderophore-producing bacteria isolated from marine environments

Zeng, X. G., Li, G., Du, Y., Yu, T., Lai, Q., Wang, L., & Shao, Z. (2025) · Acta Oceanologica Sinica · doi:10.1007/s13131-025-2472-6 · Cited by 4

Comparative Genomic Analyses of the Genus Photobacterium Illuminate Biosynthetic Gene Clusters Associated with Antagonism

Lau, N., Heng, W. L., Miswan, N., Azami, N. A., & Furusawa, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23179712 · Cited by 4

Characterization and Statistical Optimization of Enterobatin Synthesized by Escherichia coli OQ866153

Khazaal, M. T., Faraag, A. H. I., Hamada, M. A., & El-Hendawy, H. H. (2024) · Biochemical Genetics · doi:10.1007/s10528-023-10626-z · Cited by 4

Ecology shapes the genomic and biosynthetic diversification of Streptomyces bacteria from insectivorous bats

Montoya-Giraldo, M., Piper, K. R., Ikhimiukor, O. O., Park, C. J., Caimi, N. A., Buecher, D. C., Valdez, E. W., Northup, D. E., & Andam, C. P. (2024) · Microbial Genomics · doi:10.1099/mgen.0.001238 · Cited by 4

Nitrogen fertilizers activate siderophore production by the common scab causative agent Streptomyces scabiei

Stulanovic, N., Kerdel, Y., Belde, L., de Rezende, L. C. D., Deflandre, B., Burguet, P., Denoel, R., Tellatin, D., Rigolet, A., Hanikenne, M., et al. (2024) · Metallomics · doi:10.1093/mtomcs/mfae048 · Cited by 4

Antibiotic concentrations induce morphological changes and increase biofilm formation in multi-antibiotic and heavy metal resistant Kluyvera cryocrescens and Serratia fonticola

Delik, E., Eroğlu, B., Karabıyık, R., & Öztürk, B. E. T. (2024) · Microbial Pathogenesis · doi:10.1016/j.micpath.2024.107112 · Cited by 4

Siderophore-based targeted antibody recruitment for promoting immune responses towards Gram-negative pathogens

Kim, S., Park, H., Kim, D. Y., Joh, H., Oh, J. Y., Kim, D. H., Kang, M. J., Choi, C. H., & Kim, H. J. (2025) · RSC Chemical Biology · doi:10.1039/d4cb00293h · Cited by 4

Strain identity effects contribute more to Pseudomonas community functioning than strain interactions

Kramer, J., Maréchal, S., Figueiredo, A. R. T., & Kümmerli, R. (2025) · The ISME Journal · doi:10.1093/ismejo/wraf025 · Cited by 6

Lysis of Escherichia coli by colicin Ib contributes to bacterial cross-feeding by releasing active β-galactosidase

Lerminiaux, N. A., Kaufman, J. M., Schnell, L. J., Workman, S. D., Suchan, D. M., Kröger, C., Ingalls, B., & Cameron, A. D. S. (2025) · The ISME Journal · doi:10.1093/ismejo/wraf032 · Cited by 4

Iron-Derepressed Robust Production of Fusarinine C Siderophore by Aureobasidium melanogenum

Kang, X., Liu, W., Wang, X., Aslam, M. A., Liu, G.-L., & Chi, Z. (2025) · ACS Synthetic Biology · doi:10.1021/acssynbio.4c00897 · Cited by 4

Exploring the potential of repurposed deferoxamine: bridging challenges and novel formulation opportunities

Mukherjee, S., Reddy, A., Dutta, N., Vaiphei, K. K., Vivek, V., Kumar, A., & Gulbake, A. (2025) · Nanomedicine · doi:10.1080/17435889.2025.2534318 · Cited by 4

Probiotic paradox: bacillibactin from Bacillus velezensis drives pathogenic Vibrio alginolyticus proliferation through siderophore piracy

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