2009
DOI: 10.1111/j.1365-2672.2009.04345.x
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Development of a biological test to evaluate the bioavailability of iron in culture media

Abstract: Aims:  To develop an easy‐to‐use and pathogen‐free protocol giving reliable information on the bioavailability of iron in a medium. Methods and Results:  In aerobic conditions, iron bioavailability is very low, and most of its forms cannot be assimilated by micro‐organisms. Media with similar iron contents can differ considerably in iron bioavailability, something that is not easily achieved using conventional physicochemical methods. The assay developed in the present work is based on a pyoverdin siderophore … Show more

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Cited by 8 publications
(3 citation statements)
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“…Iron is essential for microorganisms due to its intervention in the synthesis of many essential components of the cell (Leclère et al, 2009). The availability of iron in the environment to living microbes is very low due to its poor solubility at neutral pH 7 (Andrews et al, 2003).…”
Section: P Phytofirmans Strain Psjn a Plant Growth Promoting Rhizobmentioning
confidence: 99%
“…Iron is essential for microorganisms due to its intervention in the synthesis of many essential components of the cell (Leclère et al, 2009). The availability of iron in the environment to living microbes is very low due to its poor solubility at neutral pH 7 (Andrews et al, 2003).…”
Section: P Phytofirmans Strain Psjn a Plant Growth Promoting Rhizobmentioning
confidence: 99%
“…Siderophores have great therapeutic (e.g., drug delivery), as well as analytical prospects [ 18 ]. However, during the last few years, only a few pyoverdine-based biosensors have been studied and developed, most of which are molecule-based [ 19 , 20 , 21 ], while only one is a whole-cell bioassay [ 22 ]. Furthermore, all of these biosensors were intended for the determination of ferric ion in medical or pharmaceutical applications.…”
Section: Introductionmentioning
confidence: 99%
“…The column eluates were monitored using a UV detector at 210 nm and gluconic acid was detected and quanti ed by comparing the retention time and peak areas obtained for pure gluconic acid standard (10 mM) subjected to similar analytical conditions. Total siderophores were quantitated using Chromo-azurol S solution assay of P4 culture supernatants and expressed as EDTA equivalents (Leclère et al 2009). Siderophore pyochelin was detected and quanti ed by HPLC using an isocratic gradient comprising of 70 % Solvent A (H 2 O, 0.1 % tri uoroacetic acid) and 30 % Solvent B (95 % acetonitrile, 0.1 % tri uoroacetic acid) and a ow rate of 1 ml/min at 254 nm (Youard et al 2007).…”
Section: Metabolite Analysismentioning
confidence: 99%