scholarly journals Concurrent Haloalkanoate Degradation and Chlorate Reduction by Pseudomonas chloritidismutans AW-1T

2017 ◽  
Vol 83 (12) ◽  
Author(s):  
Peng Peng ◽  
Ying Zheng ◽  
Jasper J. Koehorst ◽  
Peter J. Schaap ◽  
Alfons J. M. Stams ◽  
...  

ABSTRACT Haloalkanoates are environmental pollutants that can be degraded aerobically by microorganisms producing hydrolytic dehalogenases. However, there is a lack of information about the anaerobic degradation of haloalkanoates. Genome analysis of Pseudomonas chloritidismutans AW-1T, a facultative anaerobic chlorate-reducing bacterium, showed the presence of two putative haloacid dehalogenase genes, the l-DEX gene and dehI, encoding an l-2-haloacid dehalogenase (l-DEX) and a halocarboxylic acid dehydrogenase (DehI), respectively. Hence, we studied the concurrent degradation of haloalkanoates and chlorate as a yet-unexplored trait of strain AW-1T. The deduced amino acid sequences of l-DEX and DehI revealed 33 to 37% and 26 to 86% identities with biochemically/structurally characterized l-DEX and the d- and dl-2-haloacid dehalogenase enzymes, respectively. Physiological experiments confirmed that strain AW-1T can grow on chloroacetate, bromoacetate, and both l- and d-α-halogenated propionates with chlorate as an electron acceptor. Interestingly, growth and haloalkanoate degradation were generally faster with chlorate as an electron acceptor than with oxygen as an electron acceptor. In line with this, analyses of l-DEX and DehI dehalogenase activities using cell-free extract (CFE) of strain AW-1T grown on dl-2-chloropropionate under chlorate-reducing conditions showed up to 3.5-fold higher dehalogenase activity than the CFE obtained from AW-1T cells grown on dl-2-chloropropionate under aerobic conditions. Reverse transcription-quantitative PCR showed that the l-DEX gene was expressed constitutively independently of the electron donor (haloalkanoates or acetate) or acceptor (chlorate or oxygen), whereas the expression of dehI was induced by haloalkanoates. Concurrent degradation of organic and inorganic halogenated compounds by strain AW-1T represents a unique metabolic capacity in a single bacterium, providing a new piece of the puzzle of the microbial halogen cycle. IMPORTANCE Halogenated organic and inorganic compounds are important environmental pollutants that have carcinogenic and genotoxic effects on both animals and humans. Previous research studied the degradation of organic and inorganic halogenated compounds separately but not concurrently. This study shows concurrent degradation of halogenated alkanoates and chlorate as an electron donor and acceptor, respectively, coupled to growth in a single bacterium, Pseudomonas chloritidismutans AW-1T. Hence, besides biogenesis of molecular oxygen from chlorate reduction enabling a distinctive placement of strain AW-1T between aerobic and anaerobic microorganisms, we can now add another unique metabolic potential of this bacterium to the roster. The degradation of different halogenated compounds under anoxic conditions by a single bacterium is also of interest for the natural halogen cycle in different aquatic and terrestrial ecosystems where ample natural production of halogenated compounds has been documented.

Crystal compounds between potassium and well-oriented pyrolytic graphite have been prepared with a range of compositions up to saturation. Measurements have been made of changes of electrical resistance and of thermoelectric power as a function of composition in both a - and c -axis directions. Anisotropy of electrical resistance becomes smaller, and of thermoelectric power sinks to practically zero, on compound formation. Compounds between graphite and rubidium or caesium have been studied more briefly under conditions approximating to saturation. In the direction of the a -axis, the large decreases of electrical resistance observed can be interpreted on the basis that the alkali metal atoms inject electrons into the upper π -band of graphite. This is confirmed by the observed changes of thermoelectric power. Changes resemble but do not completely mirror those observed with electron acceptor compounds; the fractional transfer of electrons appears to be less complete with the electron donors. In the direction of the c -axis, intercalation of the electron donor alkali metal atoms leads to a much more striking decrease of electrical resistance than is observed with various electron acceptor groups. To supplement results previously published, brief studies are reported on crystal compounds between graphite and aluminium chloride, and graphite and iodine monochloride. Possible band models for graphite compounds with both electron donor and acceptor atoms are discussed in the light of the experimental findings.


1998 ◽  
Vol 64 (1) ◽  
pp. 352-355 ◽  
Author(s):  
M. Mackiewicz ◽  
J. Wiegel

ABSTRACT Desulfitobacterium dehalogenans grew with formate as the electron donor and 3-chloro-4-hydroxyphenylacetate (3-Cl-4-OHPA) as the electron acceptor, yielding Y X/formate,Y X/2e− , andY X/ATP ranging from 3.2 to 11.3 g of biomass (dry weight)/mol, thus indicating that energy was conserved through reductive dechlorination. Pyruvate was utilized as the electron donor and acceptor, yielding stoichiometric amounts of acetate and lactate, respectively, and a Y X/reduced acceptor of 13.0 g of biomass (dry weight)/mol. The supplementation of pyruvate-containing medium with additional electron acceptors, such as 3-Cl-4-OHPA, nitrate, fumarate, or sulfite, caused pyruvate to be replaced as the electron acceptor and nearly doubled theY X/ATP (Y X/acetate formed). A comparison of the yields for 3-Cl-4-OHPA with those for other traditional electron acceptors indicates that the dehalogenation reaction led to the formation of similar amounts of energy equivalents. The various electron acceptors were used concomitantly with 3-Cl-4-OHPA in nonacclimated cultures, but the utilization rates and amounts utilized differed.


2014 ◽  
Vol 64 (Pt_11) ◽  
pp. 3786-3791 ◽  
Author(s):  
Shungui Zhou ◽  
Guiqin Yang ◽  
Qin Lu ◽  
Min Wu

A novel Fe(III)-reducing bacterium, designated GSS01T, was isolated from a forest soil sample using a liquid medium containing acetate and ferrihydrite as electron donor and electron acceptor, respectively. Cells of strain GSS01T were strictly anaerobic, Gram-stain-negative, motile, non-spore-forming and slightly curved rod-shaped. Growth occurred at 16–40 °C and optimally at 30 °C. The DNA G+C content was 60.9 mol%. The major respiratory quinone was MK-8. The major fatty acids were C16 : 0, C18 : 0 and C16 : 1ω7c/C16 : 1ω6c. Strain GSS01T was able to grow with ferrihydrite, Fe(III) citrate, Mn(IV), sulfur, nitrate or anthraquinone-2,6-disulfonate, but not with fumarate, as sole electron acceptor when acetate was the sole electron donor. The isolate was able to utilize acetate, ethanol, glucose, lactate, butyrate, pyruvate, benzoate, benzaldehyde, m-cresol and phenol but not toluene, p-cresol, propionate, malate or succinate as sole electron donor when ferrihydrite was the sole electron acceptor. Phylogenetic analyses based on 16S rRNA gene sequences revealed that strain GSS01T was most closely related to Geobacter sulfurreducens PCAT (98.3 % sequence similarity) and exhibited low similarities (94.9–91.8 %) to the type strains of other species of the genus Geobacter . The DNA–DNA relatedness between strain GSS01T and G. sulfurreducens PCAT was 41.4±1.1 %. On the basis of phylogenetic analysis, phenotypic characterization and physiological tests, strain GSS01T is believed to represent a novel species of the genus Geobacter , and the name Geobacter soli sp. nov. is proposed. The type strain is GSS01T ( = KCTC 4545T = MCCC 1K00269T).


2018 ◽  
Vol 84 (20) ◽  
Author(s):  
Jo Philips ◽  
Niels Van den Driessche ◽  
Kim De Paepe ◽  
Antonin Prévoteau ◽  
Jeffrey A. Gralnick ◽  
...  

ABSTRACTThe involvement ofShewanellaspp. in biocorrosion is often attributed to their Fe(III)-reducing properties, but they could also affect corrosion by using metallic iron as an electron donor. Previously, we isolatedShewanellastrain 4t3-1-2LB from an acetogenic community enriched with Fe(0) as the sole electron donor. Here, we investigated its use of Fe(0) as an electron donor with fumarate as an electron acceptor and explored its corrosion-enhancing mechanism. Without Fe(0), strain 4t3-1-2LB fermented fumarate to succinate and CO2, as was shown by the reaction stoichiometry and pH. With Fe(0), strain 4t3-1-2LB completely reduced fumarate to succinate and increased the Fe(0) corrosion rate (7.0 ± 0.6)-fold in comparison to that of abiotic controls (based on the succinate-versus-abiotic hydrogen formation rate). Fumarate reduction by strain 4t3-1-2LB was, at least in part, supported by chemical hydrogen formation on Fe(0). Filter-sterilized spent medium increased the hydrogen generation rate only 1.5-fold, and thus extracellular hydrogenase enzymes appear to be insufficient to explain the enhanced corrosion rate. Electrochemical measurements suggested that strain 4t3-1-2LB did not excrete dissolved redox mediators. Exchanging the medium and scanning electron microscopy (SEM) imaging indicated that cells were attached to Fe(0). It is possible that strain 4t3-1-2LB used a direct mechanism to withdraw electrons from Fe(0) or favored chemical hydrogen formation on Fe(0) through maintaining low hydrogen concentrations. In coculture with anAcetobacteriumstrain, strain 4t3-1-2LB did not enhance acetogenesis from Fe(0). This work describes a strong corrosion enhancement by aShewanellastrain through its use of Fe(0) as an electron donor and provides insights into its corrosion-enhancing mechanism.IMPORTANCEShewanellaspp. are frequently found on corroded metal structures. Their role in microbial influenced corrosion has been attributed mainly to their Fe(III)-reducing properties and, therefore, has been studied with the addition of an electron donor (lactate).Shewanellaspp., however, can also use solid electron donors, such as cathodes and potentially Fe(0). In this work, we show that the electron acceptor fumarate supported the use of Fe(0) as the electron donor byShewanellastrain 4t3-1-2LB, which caused a (7.0 ± 0.6)-fold increase of the corrosion rate. The corrosion-enhancing mechanism likely involved cell surface-associated components in direct contact with the Fe(0) surface or maintenance of low hydrogen levels by attached cells, thereby favoring chemical hydrogen formation by Fe(0). This work sheds new light on the role ofShewanellaspp. in biocorrosion, while the insights into the corrosion-enhancing mechanism contribute to the understanding of extracellular electron uptake processes.


2020 ◽  
Vol 87 (2) ◽  
Author(s):  
Shuangyuan Liu ◽  
Jingcheng Dai ◽  
Hehong Wei ◽  
Shuyang Li ◽  
Pei Wang ◽  
...  

ABSTRACT Under anoxic conditions, many bacteria, including Shewanella loihica strain PV-4, could use nitrate as an electron acceptor for dissimilatory nitrate reduction to ammonium (DNRA) and/or denitrification. Previous and current studies have shown that DNRA is favored under higher ambient carbon-to-nitrogen (C/N) ratios, whereas denitrification is upregulated under lower C/N ratios, which is consistent with our bioenergetics calculations. Interestingly, computational analyses indicate that the common cyclic AMP receptor protein (designated CRP1) and its paralogue CRP2 might both be involved in the regulation of two competing dissimilatory nitrate reduction pathways, DNRA and denitrification, in S. loihica PV-4 and several other denitrifying Shewanella species. To explore the regulatory mechanism underlying the dissimilatory nitrate reduction (DNR) pathways, nitrate reduction of a series of in-frame deletion mutants was analyzed under different C/N ratios. Deletion of crp1 could accelerate the reduction of nitrite to NO under both low and high C/N ratios. CRP1 is not required for denitrification and actually suppresses production of NO and N2O gases. Deletion of either of the NO-forming nitrite reductase genes nirK or crp2 blocked production of NO gas. Furthermore, real-time PCR and electrophoretic mobility shift assays (EMSAs) demonstrated that the transcription levels of DNRA-relevant genes such as nap-β (napDABGH), nrfA, and cymA were upregulated by CRP1, while nirK transcription was dependent on CRP2. There are tradeoffs between the different physiological roles of nitrate/lactate, as nitrogen nutrient/carbon source and electron acceptor/donor and CRPs may leverage dissimilatory nitrate reduction pathways for maximizing energy yield and bacterial survival under ambient environmental conditions. IMPORTANCE Some microbes utilize different dissimilatory nitrate reduction (DNR) pathways, including DNR to ammonia (DNRA) and denitrification pathways, for anaerobic respiration in response to ambient carbon/nitrogen ratio changes. Large-scale industrial nitrogen fixation and fertilizer application raise the concern of emission of N2O, a stable gas with potent global warming potential, as consequence of microbial respiration, thereby aggravating global warming and climate change. However, little is known about the molecular mechanism underlying the choice of two competing DNR pathways. We demonstrate that the global regulator CRP1, which is widely encoded in bacteria, is required for DNRA in S. loihica PV-4 strain, while the CRP2 paralogue is required for transcription of the nitrite reductase gene nirK for denitrification. Sufficient carbon source lead to the predominance of DNRA, while carbon source/electron donor deficiency may result in an incomplete denitrification process, raising the concern of high levels of N2O emission from nitrate-rich and carbon source-poor waters and soils.


1989 ◽  
Vol 42 (8) ◽  
pp. 1313 ◽  
Author(s):  
DT Hurst ◽  
UB Thakrar ◽  
CHJ Wells ◽  
J Wyer

Equilibrium constants have been measured by n.m.r , spectroscopy for the electron donor- electron acceptor interaction between a number of aromatic hydrocarbons and diazines . The values obtained have shown that the interaction is weak, and that the aromatic hydrocarbon acts as the electron donor and the diazine as the electron acceptor in the systems studied. Chemical-shift data have provided evidence for the relative positioning of the donor and acceptor components within the various complexes. The effect of temperature on the equilibrium constant for complex formation between (1H6)benzene and pyrazine has shown that the enthalpy of formation is close to zero.


2013 ◽  
Vol 79 (8) ◽  
pp. 2818-2822 ◽  
Author(s):  
Sukhwan Yoon ◽  
Robert A. Sanford ◽  
Frank E. Löffler

ABSTRACTLactate but not acetate oxidation was reported to support electron acceptor reduction byShewanellaspp. under anoxic conditions. We demonstrate that the denitrifiersShewanella loihicastrain PV-4 andShewanella denitrificansOS217 utilize acetate as an electron donor for denitrification but not for fumarate or ferric iron reduction.


2019 ◽  
Vol 10 (40) ◽  
pp. 9203-9208 ◽  
Author(s):  
Yong-Jin Pu ◽  
Yuki Koyama ◽  
Daisuke Otsuki ◽  
Minjun Kim ◽  
Hiroya Chubachi ◽  
...  

We report exceptionally long-distance coupled exciplex emissions between electron-donor and electron-acceptor molecules even with a 70 nm-thick spacer layer.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Yang Liu ◽  
Fujun Zhang ◽  
Jian Wang

Organic small material lead phthalocyanine (PbPc) nanocolumns were prepared via glancing angle deposition (GLAD) on indium tin oxide (ITO) coated glass substrates. Organic electron acceptor materials fullerene (C60) was evaporated onto the nanocolumn PbPc thin films to prepare heterojunction structure ITO/PbPc/C60/Bphen/Al organic photovoltaic cells (OPVs). It is worthwhile to mention that C60molecules firstly fill the voids between PbPc nanocolumns and then form impact C60layer. The interpenetrating electron donor/acceptor structure effectively enhances interface between electron donor and electron acceptor, which is beneficial to exciton dissociation. The short circuit current density (Jsc) of organic photovoltaic devices (OPVs) based on PbPc nanocolumn was increased from 1.19 mA/cm2to 1.74 mA/cm2, which should be attributed to the increase of interface between donor and acceptor. The effect of illumination intensity on the performance of OPVs was investigated by controlling the distance between light source and sample, and theJscof two kind of OPVs was increased along with the increase of illumination intensity.


2012 ◽  
Vol 78 (23) ◽  
pp. 8304-8310 ◽  
Author(s):  
Tian Zhang ◽  
Timothy S. Bain ◽  
Kelly P. Nevin ◽  
Melissa A. Barlett ◽  
Derek R. Lovley

ABSTRACTThe abundance ofGeobacterspecies in contaminated aquifers in which benzene is anaerobically degraded has led to the suggestion that someGeobacterspecies might be capable of anaerobic benzene degradation, but this has never been documented. A strain ofGeobacter, designated strain Ben, was isolated from sediments from the Fe(III)-reducing zone of a petroleum-contaminated aquifer in which there was significant capacity for anaerobic benzene oxidation. Strain Ben grew in a medium with benzene as the sole electron donor and Fe(III) oxide as the sole electron acceptor. Furthermore, additional evaluation ofGeobacter metallireducensdemonstrated that it could also grow in benzene-Fe(III) medium. In both strain Ben andG. metallireducensthe stoichiometry of benzene metabolism and Fe(III) reduction was consistent with the oxidation of benzene to carbon dioxide with Fe(III) serving as the sole electron acceptor. With benzene as the electron donor, and Fe(III) oxide (strain Ben) or Fe(III) citrate (G. metallireducens) as the electron acceptor, the cell yields of strain Ben andG. metallireducenswere 3.2 × 109and 8.4 × 109cells/mmol of Fe(III) reduced, respectively. Strain Ben also oxidized benzene with anthraquinone-2,6-disulfonate (AQDS) as the sole electron acceptor with cell yields of 5.9 × 109cells/mmol of AQDS reduced. Strain Ben serves as model organism for the study of anaerobic benzene metabolism in petroleum-contaminated aquifers, andG. metallireducensis the first anaerobic benzene-degrading organism that can be genetically manipulated.


Sign in / Sign up

Export Citation Format

Share Document