scholarly journals Single‐cell determination of iron content in magnetotactic bacteria: implications for the iron biogeochemical cycle

2019 ◽  
Vol 22 (3) ◽  
pp. 823-831 ◽  
Author(s):  
Matthieu Amor ◽  
Mickaël Tharaud ◽  
Alexandre Gélabert ◽  
Arash Komeili
Leukemia ◽  
2005 ◽  
Vol 19 (9) ◽  
pp. 1543-1549 ◽  
Author(s):  
M R Ricciardi ◽  
T McQueen ◽  
D Chism ◽  
M Milella ◽  
E Estey ◽  
...  

2005 ◽  
Vol 99 (4) ◽  
pp. 929-939 ◽  
Author(s):  
Leonid L. Moroz ◽  
Robin L. Dahlgren ◽  
Dmitry Boudko ◽  
Jonathan V. Sweedler ◽  
Peter Lovell

2019 ◽  
Author(s):  
Matthieu Amor ◽  
Mickaël Tharaud ◽  
Alexandre Gélabert ◽  
Arash Komeili

Magnetotactic bacteria (MTB) are ubiquitous aquatic microorganisms that biomineralize dissolved iron from the environment into intracellular nanoparticles of magnetite [Fe(II)Fe(III)2O4] or greigite [Fe(II)Fe(III)2S4] in a genetically controlled manner. After cell death, these magnetite and greigite crystals are trapped into sediments which effectively removes iron from the soluble pool. MTB may significantly impact the iron biogeochemical cycle, especially in the ocean where dissolved iron limits nitrogen fixation and primary productivity. Although MTB are ubiquitous in the environment, their impact on the biogeochemical cycling of metallic elements is still poorly constrained. A thorough assessment of the mass of iron incorporated by MTB has been hampered by a lack of methodology to accurately measure the amount of, and variability in, their intracellular iron content. Here, we quantify the mass of iron contained in single MTB cells of the model organism, Magnetospirillum magneticum sp. AMB-1, using a time-resolved mass spectrometry methodology. Bacterial iron content depends on the external iron concentration, and reaches a maximum value of 10-6 ng of iron per cell when bacteria are cultivated with initial iron concentrations of 100 μM or higher. From our experimental results, we calculated the flux of dissolved iron incorporation into natural MTB populations and conclude that MTB may mineralize a significant fraction of environmental dissolved iron into crystals.


2020 ◽  
Vol 26 (4) ◽  
pp. 207-215 ◽  
Author(s):  
Diwakar Turaga ◽  
Oriane B. Matthys ◽  
Tracy A. Hookway ◽  
David A. Joy ◽  
Meredith Calvert ◽  
...  

1961 ◽  
Vol 38 (4) ◽  
pp. 545-562 ◽  
Author(s):  
L. Kecskés ◽  
F. Mutschler ◽  
I. Glós ◽  
E. Thán ◽  
I. Farkas ◽  
...  

ABSTRACT 1. An indirect paperchromatographic method is described for separating urinary oestrogens; this consists of the following steps: acidic hydrolysis, extraction with ether, dissociation of phenol-fractions with partition between the solvents. Previous purification of phenol fraction with the aid of paperchromatography. The elution of oestrogen containing fractions is followed by acetylation. Oestrogen acetate is isolated by re-chromatography. The chromatogram was developed after hydrolysis of the oestrogens 'in situ' on the paper. The quantity of oestrogens was determined indirectly, by means of an iron-reaction, after the elution of the iron content of the oestrogen spot, which was developed by the Jellinek-reaction. 2. The method described above is satisfactory for determining urinary oestrogen, 17β-oestradiol and oestriol, but could include 16-epioestriol and other oestrogenic metabolites. 3. The sensitivity of the method is 1.3–1.6 μg/24 hours. 4. The quantitative and qualitative determination of urinary oestrogens with the above mentioned method was performed in 50 pregnant and 9 non pregnant women, and also in 2 patients with granulosa cell tumour.


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