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Microbiology 143 (1997), 3625-3631; DOI  10.1099/00221287-143-11-3625
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Iron uptake in Ustilago maydis: studies with fluorescent ferrichrome analogues

Orly Ardon1, Haim Weizman3, Jacqueline Libman3,§, Abraham Shanzer3, Yona Chen2 and Yitzhak Hadar2,4

1Department of Plant Pathology and Microbiology and The Otto Warburg Center for Agricultural Biotechnology, The Hebrew University of Jerusalem, Faculty of Agricultural, Food and Environmental Quality Sciences, Rehovot 76100, Israel
2Department of Soil and Water Sciences, The Hebrew University of Jerusalem, Faculty of Agricultural, Food and Environmental Quality Sciences, Rehovot 76100, Israel
3Department of Organic Chemistry, The Weizmann Institute of Science, Rehovot 76100, Israel

4 Author for correspondence: Yitzhak Hadar. Tel: +972 8 9481315. Fax: +972 8 9468785. e-mail: HADAR@AGRI.HUJI.AC.IL

ABSTRACT

Iron uptake by the phytopathogenic fungus Ustilago maydis was studied using synthetic biomimetic ferrichrome analogues and their fluorescently labelled derivatives as structural and dynamic probes, respectively. The use of structurally distinct analogues enabled determination of the structural requirements for recognition by the fungal iron-uptake system. The application of fluorescently labelled derivatives which convert from a non-fluorescent to a fluorescent state upon iron (III) release enabled monitoring of iron uptake in real time both fluorimetrically and microscopically. Different rates of 55Fe uptake were found for two structurally distinct synthetic analogues, B9 and B5, which differ in their amino acid building blocks. B9 mediated uptake of 55Fe at a higher rate than B5. The behaviour of the fluorescent derivatives B9-Ant (anthracene-labelled B9) and B5-Ant (anthracene-labelled B5) paralleled that of their non-labelled precursors. Exposure of fungal cells to B9-Ant led to a higher increase of fluorescence in the medium than exposure to B5-Ant, indicating a more effective iron uptake from B9-Ant. By using fluorescence microscopy it was possible to trace the label of B9-Ant. Fluorescence was localized in regularly shaped vesicles in the treated cells. The rate of fluorescence appearance within the cells lagged behind the rate of iron uptake, suggesting use of the siderophores for iron storage.


Keywords: fungal iron uptake, ferrichrome, fluorescent biomimetic siderophores, fluorescence microscopy

§ Present address: Dr Jacqueline Libman passed away on 30 March 1997, while this article was being prepared. This article is dedicated to her memory.




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