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Enlightening mineral iron sensing in Pseudomonas fluorescens by surface active maghemite nanoparticles: Involvement of the OprF porin

M. Magro, L. Fasolato, E. Bonaiuto, NA. Andreani, D. Baratella, V. Corraducci, G. Miotto, B. Cardazzo, F. Vianello,

. 2016 ; 1860 (10) : 2202-10. [pub] 20160504

Language English Country Netherlands

Document type Journal Article, Research Support, Non-U.S. Gov't

BACKGROUND: Mineral iron(III) recognition by bacteria is considered a matter of debate. The peculiar surface chemistry of novel naked magnetic nanoparticles, called SAMNs (surface active maghemite nanoparticles) characterized by solvent exposed Fe(3+) sites on their surface, was exploited for studying mineral iron sensing in Pseudomonas fluorescens. METHODS: SAMNs were applied for mimicking Fe(3+) ions in solution, acting as magnetically drivable probes to evaluate putative Fe(3+) recognition sites on the microorganism surface. Culture broths and nano-bio-conjugates were characterized by UV-Vis spectroscopy and mass spectrometry. RESULTS: The whole heritage of a membrane porin (OprF) of P. fluorescens Ps_22 cells was recognized and firmly bound by SAMNs. The binding of nanoparticles to OprF porin was correlated to a drastic inhibition of a siderophore (pyoverdine) biosynthesis and to the stimulation of the production and rate of formation of a secondary siderophore. The analysis of metabolic pathways, based on P. fluorescens Ps_22 genomic information, evidenced that this putative secondary siderophore does not belong to a selection of the most common siderophores. CONCLUSIONS: In the scenario of an adhesion mechanism, it is plausible to consider OprF as the biological component deputed to the mineral iron sensing in P. fluorescens Ps_22, as well as one key of siderophore regulation. GENERAL SIGNIFICANCE: The present work sheds light on mineral iron sensing in microorganisms. Peculiar colloidal naked iron oxide nanoparticles offer a useful approach for probing the adhesion of bacterial surface on mineral iron for the identification of the specific recognition site for this iron uptake regulation in microorganisms.

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$a Magro, Massimiliano $u Department of Comparative Biomedicine and Food Science, University of Padova, Italy; Regional Centre of Advanced Technologies and Materials, Department of Physical Chemistry, Palacky University in Olomouc, Czech Republic. Electronic address: massimiliano.magro@unipd.it.
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$a BACKGROUND: Mineral iron(III) recognition by bacteria is considered a matter of debate. The peculiar surface chemistry of novel naked magnetic nanoparticles, called SAMNs (surface active maghemite nanoparticles) characterized by solvent exposed Fe(3+) sites on their surface, was exploited for studying mineral iron sensing in Pseudomonas fluorescens. METHODS: SAMNs were applied for mimicking Fe(3+) ions in solution, acting as magnetically drivable probes to evaluate putative Fe(3+) recognition sites on the microorganism surface. Culture broths and nano-bio-conjugates were characterized by UV-Vis spectroscopy and mass spectrometry. RESULTS: The whole heritage of a membrane porin (OprF) of P. fluorescens Ps_22 cells was recognized and firmly bound by SAMNs. The binding of nanoparticles to OprF porin was correlated to a drastic inhibition of a siderophore (pyoverdine) biosynthesis and to the stimulation of the production and rate of formation of a secondary siderophore. The analysis of metabolic pathways, based on P. fluorescens Ps_22 genomic information, evidenced that this putative secondary siderophore does not belong to a selection of the most common siderophores. CONCLUSIONS: In the scenario of an adhesion mechanism, it is plausible to consider OprF as the biological component deputed to the mineral iron sensing in P. fluorescens Ps_22, as well as one key of siderophore regulation. GENERAL SIGNIFICANCE: The present work sheds light on mineral iron sensing in microorganisms. Peculiar colloidal naked iron oxide nanoparticles offer a useful approach for probing the adhesion of bacterial surface on mineral iron for the identification of the specific recognition site for this iron uptake regulation in microorganisms.
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$a Fasolato, Luca $u Department of Comparative Biomedicine and Food Science, University of Padova, Italy. Electronic address: luca.fasolato@unipd.it.
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$a Bonaiuto, Emanuela $u Department of Comparative Biomedicine and Food Science, University of Padova, Italy. Electronic address: emanuela.bonaiuto@unidp.it.
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$a Andreani, Nadia Andrea $u Department of Comparative Biomedicine and Food Science, University of Padova, Italy. Electronic address: nadiaandrea.andreani@studenti.unipd.it.
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$a Baratella, Davide $u Department of Comparative Biomedicine and Food Science, University of Padova, Italy. Electronic address: davide.baratella@studenti.unipd.it.
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$a Corraducci, Vittorino $u Department of Comparative Biomedicine and Food Science, University of Padova, Italy. Electronic address: vittorino.corraducci@unipd.it.
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$a Miotto, Giovanni $u Department of Molecular Medicine, University of Padova, Italy. Electronic address: gianni.miotto@unipd.it.
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$a Cardazzo, Barbara $u Department of Comparative Biomedicine and Food Science, University of Padova, Italy. Electronic address: barbara.cardazzo@unipd.it.
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$a Vianello, Fabio $u Department of Comparative Biomedicine and Food Science, University of Padova, Italy; Regional Centre of Advanced Technologies and Materials, Department of Physical Chemistry, Palacky University in Olomouc, Czech Republic. Electronic address: fabio.vianello@unipd.it.
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