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Curium(III) complexation with pyoverdins secreted by a groundwater strain of Pseudomonas fluorescens
Authors:Henry Moll  Anna Johnsson  Mathias Schäfer  Karsten Pedersen  Herbert Budzikiewicz  Gert Bernhard
Affiliation:1. Institute of Radiochemistry, Forschungszentrum Dresden-Rossendorf, P.O. Box 510119, Dresden, 01314, Germany
2. Department of Cell and Molecular Biology, Microbiology, G?teborg University, P.O. Box 462, G?teborg, 405 30, Sweden
3. Institut für Organische Chemie, Universit?t zu K?ln, Greinstra?e 4, Koln, 50939, Germany
Abstract:Pyoverdins, bacterial siderophores produced by ubiquitous fluorescent Pseudomonas species, have great potential to bind and thus transport actinides in the environment. Therefore, the influence of pyoverdins secreted by microbes on the migration processes of actinides must be taken into account in strategies for the risk assessment of potential nuclear waste disposal sites. The unknown interaction between curium(III) and the pyoverdins released by Pseudomonas fluorescens (CCUG 32456) isolated from the granitic rock aquifers at the Äspö Hard Rock Laboratory (Äspö HRL), Sweden, is the subject of this paper. The interaction between soluble species of curium(III) and pyoverdins was studied at trace curium(III) concentrations (3 × 10?7 M) using time-resolved laser-induced fluorescence spectroscopy (TRLFS). Three Cm3+P. fluorescens (CCUG 32456) pyoverdin species, MpHqLr, could be identified from the fluorescence emission spectra, CmH2L+, CmHL, and CmL?, having peak maxima at 601, 607, and 611 nm, respectively. The large formation constants, log β121 = 32.50 ± 0.06, log β111 = 27.40 ± 0.11, and log β101 = 19.30 ± 0.17, compared to those of other chelating agents illustrate the unique complexation properties of pyoverdin-type siderophores. An indirect excitation mechanism for the curium(III) fluorescence was observed in the presence of the pyoverdin molecules.
Keywords:Curium  Pyoverdin  Fluorescence spectroscopy  TRLFS  Complexation
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