Research Support, Non-U.S. Gov'ts
- Dimethyl sulfoxide reduction by a hyperhermophilic archaeon Thermococcus onnurineus NA1 via a cysteine-cystine redox shuttle
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Ae Ran Choi , Min-Sik Kim , Sung Gyun Kang , Hyun Sook Lee
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J. Microbiol. 2016;54(1):31-38. Published online January 5, 2016
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DOI: https://doi.org/10.1007/s12275-016-5574-1
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Abstract
- A variety of microbes grow by respiration with dimethyl sulfoxide
(DMSO) as an electron acceptor, and several distinct
DMSO respiratory systems, consisting of electron carriers
and a terminal DMSO reductase, have been characterized.
The heterotrophic growth of a hyperthermophilic archaeon
Thermococcus onnurineus NA1 was enhanced by the addition
of DMSO, but the archaeon was not capable of reducing
DMSO to DMS directly using a DMSO reductase. Instead, the
archaeon reduced DMSO via a cysteine-cystine redox shuttle
through a mechanism whereby cystine is microbially reduced
to cysteine, which is then reoxidized by DMSO reduction.
A thioredoxin reductase-protein disulfide oxidoreductase
redox couple was identified to have intracellular cystine-reducing
activity, permitting recycle of cysteine. This study presents
the first example of DMSO reduction via an electron
shuttle. Several Thermococcales species also exhibited enhanced
growth coupled with DMSO reduction, probably by
disposing of excess reducing power rather than conserving
energy.
- Thionine Increases Electricity Generation from Microbial Fuel Cell Using Saccharomyces cerevisiae and Exoelectrogenic Mixed Culture
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Mostafa Rahimnejad , Ghasem Darzi Najafpour , Ali Asghar Ghoreyshi , Farid Talebnia , Giuliano C. Premier , Gholamreza Bakeri , Jung Rae Kim , Sang-Eun Oh
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J. Microbiol. 2012;50(4):575-580. Published online August 25, 2012
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DOI: https://doi.org/10.1007/s12275-012-2135-0
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90
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Abstract
- Microbial fuel cells (MFCs) have been shown to be capable of clean energy production through the oxidation of biodegradable organic waste using various bacterial species as biocatalysts. In this study we found Saccharomyces cerevisiae, previously known electrochemcially inactive or less active species, can be acclimated with an electron mediator thionine for electrogenic biofilm formation in MFC, and electricity production is improved with facilitation of electron transfer. Power generation of MFC was also significantly increased by thionine with both aerated and non-aerated cathode. With electrochemically active biofilm enriched with swine wastewater, MFC power increased more significantly by addition of thionine. The optimum mediator concentration was 500 mM of thionine with S. cerevisae in MFC with the maximum voltage and current generation in the microbial fuel cell were 420 mV and 700 mA/m2, respectively. Cyclic voltametry shows that thionine improves oxidizing and reducing capability in both pure culture and acclimated biofilm as compared to non-mediated cell. The results obtained indicated that thionine has great potential to enhance power generation from unmediated yeast or electrochemically active biofilm in MFC.
- Effect of Natural Mediators on the Stability of Trametes trogii Laccase during the Decolourization of Textile Wastewaters
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Rim Khlifi-Slama , Tahar Mechichi , Sami Sayadi , Abdelhafidh Dhouib
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J. Microbiol. 2012;50(2):226-234. Published online April 27, 2012
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DOI: https://doi.org/10.1007/s12275-012-1421-1
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Abstract
- The purpose of the present study was to determine the
effect of natural mediators on the stability of the Trametes
trogii crude laccase in the process of decolourization of
textile effluents. Acetosyringone allowed the highest wastewaters
decolourization rate of 25%. At higher concentrations
of acetosyringone, the relative activity of laccase decreased
approximately by between 38% and 88% after 5 days of
incubation. T. trogii laccase was strongly inactivated at 3
mM syringaldehyde, after 3 days of incubation. However,
laccase activity is more stable in the presence of the vanillin
and m-coumarate. The T. trogii growth on solid effluentbased-
medium was examined and evaluated by measuring
the colony diameter in cm. T. trogii was completely inhibited
on 100:0 and 80:20 effluent:water solid medium, however,
colony diameter reached 5 cm on 60:40 effluent:water solid
medium after 13–14 days incubation. When the textile effluent
was pre-treated with laccase and laccase-acetosyringone
system, the colony diameter of 2 cm of T. trogii on 80:20
effluent:water solid medium was reached after 14 and 10
days of incubation respectively.