Literature DB >> 2125501

Bacterial siderophores: structures of pyoverdins Pt, siderophores of Pseudomonas tolaasii NCPPB 2192, and pyoverdins Pf, siderophores of Pseudomonas fluorescens CCM 2798. Identification of an unusual natural amino acid.

P Demange1, A Bateman, C Mertz, A Dell, Y Piémont, M A Abdallah.   

Abstract

Pyoverdins were isolated and characterized respectively from the cultures of Pseudomonas tolaasii NCPPB 2192 (pyoverdins Pt, Pt A, and Pt B) and Pseudomonas fluorescens CCM 2798 (Pyoverdins Pf/1, Pf/2, Pf, Pf/3/1, and Pf/3/2) each grown in iron-deficient conditions. Their structures were established by using FAB-MS, NMR, and CD techniques. These siderophores are chromopeptides, and all but one (pyoverdin Pf/3/3) possess at the N-terminal end of their peptide chain the same chromophore that has been reported in pyoverdin Pa from Pseudomonas aeruginosa ATCC 15692 [Wendenbaum, S., Demange, P., Dell, A., Meyer, J. M., & Abdallah, M. A. (1983) Tetrahedron Lett. 24, 4877-4880] and pseudobactin B 10 from Pseudomonas B10 [Teintze, M., Hossain, M. B., Barnes, C. L., Leong, J., & Van der Helm, D. (1981) Biochemistry 20, 6446-6457] which is derived from 2,3-diamino-6,7-dihydroxyquinoline. In pyoverdins Pt this chromophore is bound to a linear peptide chain D-Ser-L-Lys-L-Ser-D-Ser-L-Thr-D-Ser-L-OHOrn-L-Thr-D-Ser-D-OHOrn (cyclic) which has its C-terminal end blocked by cyclic D-N delta-hydroxyornithine. In pyoverdins Pf, the peptide chain is also linear, SerCTHPMD-Gly-L-Ser-D-threo-OHAsp-L-Ala-Gly-D-Ala-Gly-L-O HOrn(cyclic), and contains an unusual natural amino acid which is the result of the condensation of 1 mol of serine and 1 mol of 2,4-diaminobutyric acid, forming a cyclic amidine. The pyoverdins Pt differ only in substituent bound to the nitrogen on C-3 of the chromophore, which is succinic acid in pyoverdin Pt A, succinamide in pyoverdin Pt, and alpha-ketoglutaric acid bound to the chromophore by its C-5 carbon atom in pyoverdin Pt B. Similarly, pyoverdin Pf/1, pyoverdin Pf/2, pyoverdin Pf (the major compound), and pyoverdin Pf/3/2 are substituted respectively by L-malic acid, succinic acid, L-malic amide, and succinamide. Pyoverdin Pf/3/3 has the same chromophore as azotobactin, the peptidic siderophore of Azotobacter vinelandii. These pyoverdins are very similar to pseudobactin B 10, the siderophore of Pseudomonas B10: they are linear peptides containing three bidentate groups strongly chelating Fe(III) and blocked at their N-terminal end by the catecholic chromophore and at their C-terminal end by cyclic N delta-hydroxyornithine. They differ therefore from other pyoverdins such as those from P. aeruginosa ATCC 15692 which contain a partly cyclic peptide [Briskot, G., Taraz, K., & Budzikiewicz, H. (1989) Liebigs Ann. Chem., 375-384].

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Year:  1990        PMID: 2125501     DOI: 10.1021/bi00502a005

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  12 in total

1.  Production and comparison of peptide siderophores from strains of distantly related pathovars of Pseudomonas syringae and Pseudomonas viridiflava LMG 2352.

Authors:  A Bultreys; I Gheysen
Journal:  Appl Environ Microbiol       Date:  2000-01       Impact factor: 4.792

2.  The periplasmic transaminase PtaA of Pseudomonas fluorescens converts the glutamic acid residue at the pyoverdine fluorophore to α-ketoglutaric acid.

Authors:  Michael T Ringel; Gerald Dräger; Thomas Brüser
Journal:  J Biol Chem       Date:  2017-09-14       Impact factor: 5.157

3.  Interaction of TonB with the outer membrane receptor FpvA of Pseudomonas aeruginosa.

Authors:  Hendrik Adams; Gabrielle Zeder-Lutz; Isabelle Schalk; Franc Pattus; Hervé Celia
Journal:  J Bacteriol       Date:  2006-08       Impact factor: 3.490

4.  Application of siderotyping for characterization of Pseudomonas tolaasii and "Pseudomonas reactans" isolates associated with brown blotch disease of cultivated mushrooms.

Authors:  P Munsch; V A Geoffroy; T Alatossava; J M Meyer
Journal:  Appl Environ Microbiol       Date:  2000-11       Impact factor: 4.792

5.  The copper chelator methanobactin from Methylosinus trichosporium OB3b binds copper(I).

Authors:  Amanda S Hakemian; Christine E Tinberg; Kalyan C Kondapalli; Joshua Telser; Brian M Hoffman; Timothy L Stemmler; Amy C Rosenzweig
Journal:  J Am Chem Soc       Date:  2005-12-14       Impact factor: 15.419

6.  Antagonistic Effect of Pseudomonas sp. CMI-1 on
Foodborne Pathogenic Listeria monocytogenes.

Authors:  Ágnes Belák; Anna Maráz
Journal:  Food Technol Biotechnol       Date:  2015-06       Impact factor: 3.918

7.  Dual pathways for copper uptake by methanotrophic bacteria.

Authors:  Ramakrishnan Balasubramanian; Grace E Kenney; Amy C Rosenzweig
Journal:  J Biol Chem       Date:  2011-09-07       Impact factor: 5.157

8.  Identification and characterization of a locus which regulates multiple functions in Pseudomonas tolaasii, the cause of brown blotch disease of Agaricus bisporus.

Authors:  S I Grewal; B Han; K Johnstone
Journal:  J Bacteriol       Date:  1995-08       Impact factor: 3.490

9.  Purification of Pyoverdines of Pseudomonas fluorescens 2-79 by Copper-Chelate Chromatography.

Authors:  R Xiao; W S Kisaalita
Journal:  Appl Environ Microbiol       Date:  1995-11       Impact factor: 4.792

10.  Characterization of a high-affinity iron transport system in Acinetobacter baumannii.

Authors:  J R Echenique; H Arienti; M E Tolmasky; R R Read; R J Staneloni; J H Crosa; L A Actis
Journal:  J Bacteriol       Date:  1992-12       Impact factor: 3.490

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