Literature DB >> 22393938

Exploiting bacterial iron acquisition: siderophore conjugates.

Cheng Ji1, Raúl E Juárez-Hernández, Marvin J Miller.   

Abstract

Siderophores are chelators synthesized by bacteria and fungi to sequester iron, which is essential for virulence and pathogenicity. Since the process involves active transport, which is highly regulated, remarkably efficient and often microbially selective, it has been exploited as a Trojan Horse method for development of microbe-selective antibiotics. Siderophores also have significant potential for the development of imaging contrast agents and diagnostics for pathogen-selective detection. These promising results demonstrate the versatility of natural and synthetic microbial iron chelators and their potential therapeutic applications.

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Year:  2012        PMID: 22393938      PMCID: PMC6901097          DOI: 10.4155/fmc.11.191

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  54 in total

1.  Design and synthesis of a siderophore conjugate as a potent PSMA inhibitor and potential diagnostic agent for prostate cancer.

Authors:  Pingyu Ding; Paul Helquist; Marvin J Miller
Journal:  Bioorg Med Chem       Date:  2007-11-17       Impact factor: 3.641

Review 2.  Microcins, gene-encoded antibacterial peptides from enterobacteria.

Authors:  Sophie Duquesne; Delphine Destoumieux-Garzón; Jean Peduzzi; Sylvie Rebuffat
Journal:  Nat Prod Rep       Date:  2007-04-18       Impact factor: 13.423

Review 3.  Siderophore-based iron acquisition and pathogen control.

Authors:  Marcus Miethke; Mohamed A Marahiel
Journal:  Microbiol Mol Biol Rev       Date:  2007-09       Impact factor: 11.056

4.  Total synthesis of desferrisalmycin B.

Authors:  Li Dong; John M Roosenberg; Marvin J Miller
Journal:  J Am Chem Soc       Date:  2002-12-18       Impact factor: 15.419

5.  Semisynthetic beta-lactam antibiotics. III. Effect on antibacterial activity and comt-susceptibility of chlorine-introduction into the catechol nucleus of 6-[(R)-2-[3-(3,4-dihydroxybenzoyl)-3-(3-hydroxypropyl)-1-ureido]-2- phenylacetamido]penicillanic acid.

Authors:  N Ohi; B Aoki; T Kuroki; M Matsumoto; K Kojima; T Nehashi
Journal:  J Antibiot (Tokyo)       Date:  1987-01       Impact factor: 2.649

6.  Multivalent carbocyanine molecular probes: synthesis and applications.

Authors:  Yunpeng Ye; Sharon Bloch; Jeffery Kao; Samuel Achilefu
Journal:  Bioconjug Chem       Date:  2005 Jan-Feb       Impact factor: 4.774

7.  Synthesis and biological activity of tris- and tetrakiscatecholate siderophores based on poly-aza alkanoic acids or alkylbenzoic acids and their conjugates with beta-lactam antibiotics.

Authors:  Lothar Heinisch; Steffen Wittmann; Thomas Stoiber; Ina Scherlitz-Hofmann; Dorothe Ankel-Fuchs; Ute Möllmann
Journal:  Arzneimittelforschung       Date:  2003

8.  Selective capture and identification of pathogenic bacteria using an immobilized siderophore.

Authors:  Derek D Doorneweerd; Walter A Henne; Ronald G Reifenberger; Philip S Low
Journal:  Langmuir       Date:  2010-10-05       Impact factor: 3.882

Review 9.  Microbial iron acquisition: marine and terrestrial siderophores.

Authors:  Moriah Sandy; Alison Butler
Journal:  Chem Rev       Date:  2009-10       Impact factor: 60.622

10.  Effects of siderophores on the growth of Pseudomonas aeruginosa in human serum and transferrin.

Authors:  R Ankenbauer; S Sriyosachati; C D Cox
Journal:  Infect Immun       Date:  1985-07       Impact factor: 3.441

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  42 in total

1.  Siderophore-fluoroquinolone conjugates containing potential reduction-triggered linkers for drug release: synthesis and antibacterial activity.

Authors:  Cheng Ji; Marvin J Miller
Journal:  Biometals       Date:  2015-02-08       Impact factor: 2.949

2.  Iminoguanidines as Allosteric Inhibitors of the Iron-Regulated Heme Oxygenase (HemO) of Pseudomonas aeruginosa.

Authors:  Geoffrey A Heinzl; Weiliang Huang; Wenbo Yu; Bennett J Giardina; Yue Zhou; Alexander D MacKerell; Angela Wilks; Fengtian Xue
Journal:  J Med Chem       Date:  2016-07-11       Impact factor: 7.446

Review 3.  Recent trends in the structural revision of natural products.

Authors:  Bhuwan Khatri Chhetri; Serge Lavoie; Anne Marie Sweeney-Jones; Julia Kubanek
Journal:  Nat Prod Rep       Date:  2018-06-20       Impact factor: 13.423

4.  Promysalin Elicits Species-Selective Inhibition of Pseudomonas aeruginosa by Targeting Succinate Dehydrogenase.

Authors:  Colleen E Keohane; Andrew D Steele; Christian Fetzer; Jittasak Khowsathit; Daria Van Tyne; Lucile Moynié; Michael S Gilmore; John Karanicolas; Stephan A Sieber; William M Wuest
Journal:  J Am Chem Soc       Date:  2018-01-24       Impact factor: 15.419

5.  Determination of the Molecular Structures of Ferric Enterobactin and Ferric Enantioenterobactin Using Racemic Crystallography.

Authors:  Timothy C Johnstone; Elizabeth M Nolan
Journal:  J Am Chem Soc       Date:  2017-10-17       Impact factor: 15.419

Review 6.  Targeting iron assimilation to develop new antibacterials.

Authors:  Timothy L Foley; Anton Simeonov
Journal:  Expert Opin Drug Discov       Date:  2012-07-19       Impact factor: 6.098

7.  Siderophore-based immunization strategy to inhibit growth of enteric pathogens.

Authors:  Martina Sassone-Corsi; Phoom Chairatana; Tengfei Zheng; Araceli Perez-Lopez; Robert A Edwards; Michael D George; Elizabeth M Nolan; Manuela Raffatellu
Journal:  Proc Natl Acad Sci U S A       Date:  2016-11-07       Impact factor: 11.205

Review 8.  Beyond iron: non-classical biological functions of bacterial siderophores.

Authors:  Timothy C Johnstone; Elizabeth M Nolan
Journal:  Dalton Trans       Date:  2015-04-14       Impact factor: 4.390

9.  Biscatecholate-monohydroxamate mixed ligand siderophore-carbacephalosporin conjugates are selective sideromycin antibiotics that target Acinetobacter baumannii.

Authors:  Timothy A Wencewicz; Marvin J Miller
Journal:  J Med Chem       Date:  2013-05-08       Impact factor: 7.446

10.  Trihydroxamate siderophore-fluoroquinolone conjugates are selective sideromycin antibiotics that target Staphylococcus aureus.

Authors:  Timothy A Wencewicz; Timothy E Long; Ute Möllmann; Marvin J Miller
Journal:  Bioconjug Chem       Date:  2013-02-14       Impact factor: 4.774

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