The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.
Synthesis, nature and utility of universal iron chelator – Siderophore: A review
Open accessAbstract
Siderophores, the secondary metabolite of various microorganisms are ferric ion specific chelators secreted under iron stressed condition. These non-ribosomal peptides have been classified as catecholate, hydroxamate, carboxylate and mixed types. Recent studies focus on discovery of possible mammalian siderophores. The biosynthesis pathway including non-ribosomal dependent as well as non-ribosomal independent pathways are of great interest now a days. Many significant roles of siderophores such as virulence in pathogens, oxidative stress tolerance, classification of organisms etc. are being discovered. Studies on siderophore utilization in bioremediation and other heavy metal chelation have increased in past decade. The iron chelation ability of siderophores is being recently studied with regards to malignant cancerous cells. Not only this, it has been found that they possess antimicrobial properties which can be utilized against number of microbes. This review covers all recent aspects of siderophore and its applications.
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Enterobactin: an archetype for microbial iron transport.
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Chemical aspects of siderophore mediated iron transport
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Distinct Roles for Intra- and Extracellular Siderophores during Aspergillus fumigatus Infection
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How pathogenic bacteria evade mammalian sabotage in the battle for iron
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Microbial siderophore-mediated transport.
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“It consists of N5acyl-N5-Hydroxyornithine or N6-acyl-N6-Hydroxylysine (Winkelmann, 2002).”
InfluentialHapX-Mediated Adaption to Iron Starvation Is Crucial for Virulence of Aspergillus fumigatus
Schrettl, M., Beckmann, N., Varga, J., Heinekamp, T., Jacobsen, I. D., Jöchl, C., Moussa, T. A., Wang, S., Gsaller, F., Blatzer, M., et al. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001124 · Cited by 284
Interplay between Siderophores and Colibactin Genotoxin Biosynthetic Pathways in Escherichia coli
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Cited by
Tyśkiewicz, R., Nowak, A., Ozimek, E., & Jaroszuk-Ściseł, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042329 · Cited by 632
Bioremediation of environmental wastes: the role of microorganisms
Ayilara, M. S., & Babalola, O. O. (2023) · Frontiers in Agronomy · doi:10.3389/fagro.2023.1183691 · Cited by 437
Pratush, A., Kumar, A., & Hu, Z. (2018) · International Microbiology · doi:10.1007/s10123-018-0012-3 · Cited by 399
Virulence Factors in Hypervirulent Klebsiella pneumoniae
Zhu, J., Wang, T., Chen, L., & Du, H. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.642484 · Cited by 320
Cefiderocol: A Novel Agent for the Management of Multidrug-Resistant Gram-Negative Organisms
Wu, J. Y., Srinivas, P., & Pogue, J. M. (2020) · Infectious Diseases and Therapy · doi:10.1007/s40121-020-00286-6 · Cited by 195
Metadata
- Authors
- Khan, A., Singh, P., & Srivastava, A.
- Venue
- Microbiological Research
- Publisher
- Elsevier BV
- Published
- 2018-07
- Volume
- 212-213
- Pages
- 103-111
- ISSN
- 0944-5013 (ISSN-L)
- OpenAlex
- W2765117954
- Cited by
- 413
- References
- 11
- FWCI
- 11.12
- Type
- journal article
- Language
- en
- Open access
- bronze
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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