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

Cupriavidus necator H16 is known to be a rich source of linear lipopeptide siderophores when grown under iron-depleted conditions; prior literature termed these compounds cupriachelins. These small molecules bear β-hydroxyaspartate moieties that contribute to a photoreduction of iron when bound as ferric cupriachelin. Here, we present structural assignment of cupriachelins from C. necator B-4383 grown under iron limitation. The characterization of B-4383 cupriachelins is based on MS/MS fragmentation analysis, which was confirmed by 1D- and 2D-NMR for the most abundant analog (1). The cupriachelin congeners distinguish these two strains with differences in the preferred lipid tail; however, our rigorous metabolomic investigation also revealed minor analogs with changes in the peptide core, hinting at a potential mechanism by which these siderophores may reduce biologically unavailable ferric iron (4–6). Antifungal screening of the C. necator B-4383 supernatant extract and the isolated cupriachelin analog (1) revealed inhibitory activity against Cryptococcus neoformans, with IC50 values of 16.6 and 3.2 μg/mL, respectively. This antifungal activity could be explained by the critical role of the iron acquisition pathway in the growth and pathogenesis of the C. neoformans fungal pathogen.

[1]  Paul D. Boudreau,et al.  A Universal Language for Finding Mass Spectrometry Data Patterns , 2022, bioRxiv.

[2]  G. Agrawal,et al.  Antifungal Activity of Siderophore Isolated From Escherichia coli Against Aspergillus nidulans via Iron-Mediated Oxidative Stress , 2021, Frontiers in Microbiology.

[3]  Alessandro Venditti,et al.  What is and what should never be: artifacts, improbable phytochemicals, contaminants and natural products , 2020, Natural product research.

[4]  Hong Mei Liu,et al.  Siderophore Production by Rhizosphere biological control bacteria Brevibacillus brevis GZDF3 of Pinellia ternata and its antifungal effects on Candida albicans. , 2020, Journal of microbiology and biotechnology.

[5]  B. Wang,et al.  Siderophore Production by Rhizosphere Biological Control Bacteria Brevibacillus brevis GZDF3 of Pinellia ternata and Its Antifungal Effects on Candida albicans , 2020, Journal of microbiology and biotechnology.

[6]  R. Kümmerli,et al.  Bacterial siderophores in community and host interactions , 2019, Nature Reviews Microbiology.

[7]  Zachary L Reitz,et al.  Genomic analysis of siderophore β-hydroxylases reveals divergent stereocontrol and expands the condensation domain family , 2019, Proceedings of the National Academy of Sciences.

[8]  J. P. Henderson,et al.  Uropathogenic enterobacteria use the yersiniabactin metallophore system to acquire nickel , 2018, The Journal of Biological Chemistry.

[9]  A. Butler,et al.  β-Hydroxyaspartic acid in siderophores: biosynthesis and reactivity , 2018, JBIC Journal of Biological Inorganic Chemistry.

[10]  B. Haltli,et al.  Isolation of Imaqobactin, an Amphiphilic Siderophore from the Arctic Marine Bacterium Variovorax Species RKJM285. , 2018, Journal of natural products.

[11]  Kristian Fog Nielsen,et al.  Sharing and community curation of mass spectrometry data with Global Natural Products Social Molecular Networking , 2016, Nature Biotechnology.

[12]  G. Gadd,et al.  Biomineralization, Bioremediation and Biorecovery of Toxic Metals and Radionuclides , 2016 .

[13]  F. Al-Misned,et al.  Bioremediation of Nitrate- and Arsenic-Contaminated Groundwater Using Nitrate-Dependent Fe(II) Oxidizing Clostridium sp. Strain pxl2 , 2016 .

[14]  Zhi Chen,et al.  Biomineralization of Pb(II) into Pb-hydroxyapatite induced by Bacillus cereus 12-2 isolated from Lead-Zinc mine tailings. , 2016, Journal of hazardous materials.

[15]  J. P. Henderson,et al.  Microbial Copper-binding Siderophores at the Host-Pathogen Interface* , 2015, The Journal of Biological Chemistry.

[16]  P. Lens,et al.  Selenium biomineralization for biotechnological applications. , 2015, Trends in biotechnology.

[17]  Christopher Lawrence,et al.  Iron acquisition and oxidative stress response in aspergillus fumigatus , 2015, BMC Systems Biology.

[18]  A. G. Bobrov,et al.  The Yersinia pestis siderophore, yersiniabactin, and the ZnuABC system both contribute to zinc acquisition and the development of lethal septicaemic plague in mice , 2014, Molecular microbiology.

[19]  I. Schalk,et al.  Siderophore-dependent iron uptake systems as gates for antibiotic Trojan horse strategies against Pseudomonas aeruginosa. , 2014, Metallomics : integrated biometal science.

[20]  J. Kronstad,et al.  Role of Ferric Reductases in Iron Acquisition and Virulence in the Fungal Pathogen Cryptococcus neoformans , 2013, Infection and Immunity.

[21]  Ashraf Ibrahim,et al.  Gold biomineralization by a metallophore from a gold-associated microbe. , 2013, Nature chemical biology.

[22]  D. Stahl,et al.  Verminephrobacter eiseniae gen. nov., sp. nov., a nephridial symbiont of the earthworm Eisenia foetida (Savigny). , 2013, International journal of systematic and evolutionary microbiology.

[23]  R. Kolter,et al.  Catecholate Siderophores Protect Bacteria from Pyochelin Toxicity , 2012, PloS one.

[24]  L. Sombers,et al.  Trace metal complexation by the triscatecholate siderophore protochelin: structure and stability , 2012, BioMetals.

[25]  M. Nett,et al.  Structure and biosynthetic assembly of cupriachelin, a photoreactive siderophore from the bioplastic producer Cupriavidus necator H16. , 2012, Journal of the American Chemical Society.

[26]  Duncan W. Wilson,et al.  Candida albicans iron acquisition within the host. , 2009, FEMS yeast research.

[27]  J. Kronstad,et al.  Role of Ferroxidases in Iron Uptake and Virulence of Cryptococcus neoformans , 2009, Eukaryotic Cell.

[28]  M. Gilmore,et al.  Microbial telesensing: probing the environment for friends, foes, and food. , 2009, Cell host & microbe.

[29]  Rosanne E. Frederick,et al.  Iron trafficking as an antimicrobial target , 2009, BioMetals.

[30]  R. Verpoorte,et al.  Solvent Derived Artifacts in Natural Products Chemistry , 2009, Natural product communications.

[31]  M. Marahiel,et al.  Siderophore-Based Iron Acquisition and Pathogen Control , 2007, Microbiology and Molecular Biology Reviews.

[32]  J. Kronstad,et al.  Iron Regulation of the Major Virulence Factors in the AIDS-Associated Pathogen Cryptococcus neoformans , 2006, PLoS biology.

[33]  H. Brückner,et al.  Marfey’s reagent for chiral amino acid analysis: A review , 2004, Amino Acids.

[34]  J. Ernst,et al.  Characterization of the Aspergillus nidulans transporters for the siderophores enterobactin and triacetylfusarinine C. , 2003, The Biochemical journal.

[35]  K. Harada,et al.  A Nonempirical Method Using LC/MS for Determination of the Absolute Configuration of Constituent Amino Acids in a Peptide: Elucidation of Limitations of Marfey's Method and of Its Separation Mechanism , 1997 .

[36]  C. Stammer,et al.  threo- and erythro- β-Hydroxy-DL-aspartic acids , 1969 .

[37]  J. Verhave,et al.  [Cryptococcal meningitis]. , 2015, Nederlands tijdschrift voor geneeskunde.

[38]  Clinical,et al.  Reference method for broth dilution antifungal susceptibility testing of filamentous fungi : Approved standard , 2008 .

[39]  Clinical,et al.  Reference method for broth dilution antifungal susceptibility testing of yeasts : Approved standard , 2008 .

[40]  C. Reid,et al.  Mechanisms of iron acquisition from siderophores by microorganisms and plants , 2004, Plant and Soil.

[41]  Peter Marfey,et al.  Determination ofD-amino acids. II. Use of a bifunctional reagent, 1,5-difluoro-2,4-dinitrobenzene , 1984 .