scholarly journals Tactic Response ofShewanella oneidensisMR-1 toward Insoluble Electron Acceptors

mBio ◽  
2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Joseph Oram ◽  
Lars J. C. Jeuken

ABSTRACTExoelectrogenic bacteria are defined by their ability to respire on extracellular and insoluble electron acceptors and have applications in bioremediation and microbial electrochemical systems (MESs), while playing important roles in biogeochemical cycling.Shewanella oneidensisMR-1, which has become a model organism for the study of extracellular respiration, is known to display taxis toward insoluble electron acceptors, including electrodes. Multiple mechanisms have been proposed for MR-1’s tactic behavior, and, here, we report on the role of electrochemical potential by video microscopy cell tracking experiments in three-electrode electrochemical cells. MR-1 trajectories were determined using a particle tracking algorithm and validated with Shannon’s entropy method. Tactic response by MR-1 in the electrochemical cell was observed to depend on the applied potential, as indicated by the average velocity and density of motile (>4 µm/s) MR-1 close to the electrode (<50 µm). Tactic behavior was observed at oxidative potentials, with a strong switch between the potentials −0.15 to −0.25 V versus the standard hydrogen electrode (SHE), which coincides with the reduction potential of flavins. The average velocity and density of motile MR-1 close to the electrode increased when riboflavin was added (2 µM), but were completely absent in a ΔmtrC/ΔomcAmutant of MR-1. Besides flavin’s function as an electron mediator to support anaerobic respiration on insoluble electron acceptors, we propose that riboflavin is excreted by MR-1 to sense redox gradients in its environment, aiding taxis toward insoluble electron acceptors, including electrodes in MESs.IMPORTANCEPrevious hypotheses of tactic behavior of exoelectrogenic bacteria are based on techniques that do not accurately control the electrochemical potential, such as chemical-in-plug assays or microscopy tracking experiments in two-electrode cells. Here, we have revisited previous experiments and, for the first time, performed microscopy cell-tracking experiments in three-electrode electrochemical cells, with defined electrode potentials. Based on these experiments, taxis toward electrodes is observed to switch at about −0.2 V versus standard hydrogen electrode (SHE), coinciding with the reduction potential of flavins.

1983 ◽  
Vol 38 (9-10) ◽  
pp. 701-707 ◽  
Author(s):  
Peter Nielsen ◽  
Adelbert Bacher ◽  
Diana Darling ◽  
Mark Cushman

7α,7α,7α,8α,8α,8α-Hexafluororiboflavin (4) has been prepared and its oxidation-reduction potential determined polarographically to be + 0.02 V with respect to the standard hydrogen electrode. Compound 4 does not by itself promote the growth of Lactobacillus casei. However, in the presence of low riboflavin (1) concentrations, the hexafluoro analog 4 has some growth enhancing activity. The FMN analog 7α,7α,7α,8α,8α,8α-hexafluororiboflavin 5′-phosphate (10) was also synthesized and found to bind tightly to apoflavodoxin from Megasphaera elsdenii. The dissociation constant (3.2 × 10-9m) is about one order of magnitude larger than that of FMN (1.1 × 10-10м). However, apoflavodoxin reconstituted with hexafluororiboflavin 5′-phosphate (10) has no coenzyme activity. Hexafluoro-FMN (10) was also unable to act as a coenzyme for luciferase from Photobacterium fisheri. Hexafluororiboflavin 4 did not inhibit the light riboflavin synthase from Bacillus subtilis to a significant extent {Ki> 10-4 м).


1989 ◽  
Vol 264 (1) ◽  
pp. 265-273 ◽  
Author(s):  
F A Armstrong ◽  
S J George ◽  
R Cammack ◽  
E C Hatchikian ◽  
A J Thomson

Desulfovibrio africanus ferredoxin III is a monomeric protein (Mr 6585) containing seven cysteine residues and 7-8 iron atoms and 6-8 atoms of acid-labile sulphur. It is shown that reversible unmediated electrochemistry of the two iron-sulphur clusters can be obtained by using a pyrolytic-graphite-‘edge’ carbon electrode in the presence of an appropriate aminoglycoside, neomycin or tobramycin, as promoter. Cyclic voltammetry reveals two well-defined reversible waves with E0′ = -140 +/- 10 mV and -410 +/- 5 mV (standard hydrogen electrode) at 2 degrees C. Bulk reduction confirms that each of these corresponds to a one-electron process. Low-temperature e.p.r. and magnetic-c.d. spectroscopy identify the higher-potential redox couple with a cluster of core [3Fe-4S]1+.0 and the lower with a [4Fe-4S]2+.1+ centre. The low-temperature magnetic-c.d. spectra and magnetization properties of the three-iron cluster show that it is essentially identical with that in Desulfovibrio gigas ferredoxin II. We assign cysteine-11, -17 and -51 as ligands of the [3Fe-4S] core and cysteine-21, -41, -44 and -47 to the [4Fe-4S] centre.


2004 ◽  
Vol 70 (9) ◽  
pp. 5415-5425 ◽  
Author(s):  
Charles R. Myers ◽  
Judith M. Myers

ABSTRACT The mechanisms underlying the use of insoluble electron acceptors by metal-reducing bacteria, such as Shewanella oneidensis MR-1, are currently under intensive study. Current models for shuttling electrons across the outer membrane (OM) of MR-1 include roles for OM cytochromes and the possible excretion of a redox shuttle. While MR-1 is able to release a substance that restores the ability of a menaquinone (MK)-negative mutant, CMA-1, to reduce the humic acid analog anthraquinone-2,6-disulfonate (AQDS), cross-feeding experiments conducted here showed that the substance released by MR-1 restores the growth of CMA-1 on several soluble electron acceptors. Various strains derived from MR-1 also release this substance; these include mutants lacking the OM cytochromes OmcA and OmcB and the OM protein MtrB. Even though strains lacking OmcB and MtrB cannot reduce Fe(III) or AQDS, they still release a substance that restores the ability of CMA-1 to use MK-dependent electron acceptors, including AQDS and Fe(III). Quinone analysis showed that this released substance restores MK synthesis in CMA-1. This ability to restore MK synthesis in CMA-1 explains the cross-feeding results and challenges the previous hypothesis that this substance represents a redox shuttle that facilitates metal respiration.


2012 ◽  
Vol 34 (1) ◽  
pp. 21-26 ◽  
Author(s):  
Toru Matsui ◽  
Yasutaka Kitagawa ◽  
Mitsutaka Okumura ◽  
Yasuteru Shigeta ◽  
Shigeyoshi Sakaki

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