Abstract
A synthetic siderophore, O-Trensox (L), has been designed and synthesized to improve iron nutrition of plants. The affinity for iron of this ligand [pFe(III) = 29.5 and pFe(II) = 17.9] is very high compared with EDTA. In spite of its high and specific affinity for iron, O-Trensox was found to be able to prevent, and to reverse, iron chlorosis in several plant species grown in axenic conditions. It also allows the iron nutrition and growth of Acer pseudoplatanus L. cell suspensions. The rate of iron metabolization was monitored by 59Fe radioiron. Ferritins, the iron storage proteins, are shown to be the first iron-labelled proteins during iron metabolization and to be able to further dispatch the metal. Using Fe(III)-Trensox, the rate of iron incorporation into ferritin was found to be higher than when using Fe-EDTA, but slower than with Fe-citrate, the natural iron carrier in xylem. During a plant cell culture, the extracellular concentrations of iron complex and free ligand were measured; changes in their relative amounts showed that the iron complex is dissociated extracellularly and that only iron is internalized. This suggests a high affinity for iron of a putative carrier on the plasmalemma. In contrast with Fe-citrate and Fe-EDTA complexes, Fe(III)-Trensox is not photoreducible. Its ability to induce radical damage as a Fenton reagent was tested using supercoiled DNA as target molecule. Unlike Fe-citrate and Fe-EDTA, Fe(II)-Trensox and Fe(III)-Trensox were proven to be harmless even during ascorbate-driven reduction, while Fe-EDTA and Fe-citrate generate heavy damage to DNA.
Full text
PDF






Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Allnutt F. C., Bonner W. D. Evaluation of Reductive Release as a Mechanism for Iron Uptake from Ferrioxamine B by Chlorella vulgaris. Plant Physiol. 1987 Nov;85(3):751–756. doi: 10.1104/pp.85.3.751. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Balla G., Vercellotti G. M., Eaton J. W., Jacob H. S. Iron loading of endothelial cells augments oxidant damage. J Lab Clin Med. 1990 Oct;116(4):546–554. [PubMed] [Google Scholar]
- Bar-Ness E., Hadar Y., Chen Y., Römheld V., Marschner H. Short-term effects of rhizosphere microorganisms on fe uptake from microbial siderophores by maize and oat. Plant Physiol. 1992 Sep;100(1):451–456. doi: 10.1104/pp.100.1.451. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bar-Ness E., Hadar Y., Chen Y., Shanzer A., Libman J. Iron uptake by plants from microbial siderophores : a study with 7-nitrobenz-2 oxa-1,3-diazole-desferrioxamine as fluorescent ferrioxamine B analog. Plant Physiol. 1992 Aug;99(4):1329–1335. doi: 10.1104/pp.99.4.1329. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brown J. C., Foy C. D., Bennett J. H., Christiansen M. N. Two light sources differentially affected ferric iron reduction and growth of cotton. Plant Physiol. 1979 Apr;63(4):692–695. doi: 10.1104/pp.63.4.692. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chaney R. L., Brown J. C., Tiffin L. O. Obligatory reduction of ferric chelates in iron uptake by soybeans. Plant Physiol. 1972 Aug;50(2):208–213. doi: 10.1104/pp.50.2.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jurkevitch E., Hadar Y., Chen Y., Chino M., Mori S. Indirect utilization of the phytosiderophore mugineic acid as an iron source to rhizosphere fluorescent Pseudomonas. Biometals. 1993 Summer;6(2):119–123. doi: 10.1007/BF00140113. [DOI] [PubMed] [Google Scholar]
- Laulhere J. P., Briat J. F. Iron release and uptake by plant ferritin: effects of pH, reduction and chelation. Biochem J. 1993 Mar 15;290(Pt 3):693–699. doi: 10.1042/bj2900693. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lescure A. M., Massenet O., Briat J. F. Purification and characterization of an iron-induced ferritin from soybean (Glycine max) cell suspensions. Biochem J. 1990 Nov 15;272(1):147–150. doi: 10.1042/bj2720147. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Neema C., Laulhere J. P., Expert D. Iron Deficiency Induced by Chrysobactin in Saintpaulia Leaves Inoculated with Erwinia chrysanthemi. Plant Physiol. 1993 Jul;102(3):967–973. doi: 10.1104/pp.102.3.967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tiffin L. O. Iron translocation I. Plant culture, exudate sampling, iron-citrate analysis. Plant Physiol. 1966 Mar;41(3):510–514. doi: 10.1104/pp.41.3.510. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Toyokuni S., Sagripanti J. L. Iron-mediated DNA damage: sensitive detection of DNA strand breakage catalyzed by iron. J Inorg Biochem. 1992 Aug 15;47(3-4):241–248. doi: 10.1016/0162-0134(92)84069-y. [DOI] [PubMed] [Google Scholar]