Fabrication of polypyrrole nanowire arrays-modified electrode for point-of-use water disinfection via low-voltage electroporation.

Still ∼10% of world's population has no sustainable access to centralized water supply system, causing millions of deaths annually by waterborne diseases. Here, we develop polypyrrole nanowire arrays (PPyNWs)-modified electrodes by polymerization of pyrrole on graphite felt for point-of-use water disinfection via low-voltage electroporation. A flow-through mode is specially applied to alleviate diffusion barrier of pyrrole in the porous graphite felt for uniform PPyNWs growth. The flow-through disinfection device using the optimized PPyNWs electrode achieves above 4-log removal for model virus (MS2) and gram-positive/negative bacteria (E. faecalis and E. coli) at applied voltage of 1.0 V and fluxes below 1000 and 2500 L/m2/h. Electroporation is recognized as the dominant disinfection mechanism by using square-wave alternating voltage of ±1.0 V to eliminate the electrochemical reactions. In-situ sampling experiments reveal that anode acts as the main disinfection function due to its electric field attraction with negatively charged E. coli cells. The live/dead baclight staining experiments indicate an adsorption-desorption process of E. coli cells on anode, and the adsorption-desorption balance determines the disinfection abilities of PPyNWs anode. Under 1.0 V and 2000 L/m2/h, the disinfection device enables above 4-log E. coli removal in tap water within 7-day operation with energy consumption below 20 mJ/L, suggesting its sound application potential for point-of-use water disinfection.

[Impact Mechanisms of Carboxyl Group Modified Cathode on Acetate Production in Microbial Electrosynthesis Systems].

Microbial electrosynthesis systems (MESs) can convert carbon dioxide into added value compounds using microorganisms as catalyst, which is expected to help achieve conversion of greenhouse gases into resources. However, the synthetic efficiency of MESs is far behind the industry requirements. In this study, carbon cloth surfaces were bonded with carboxyl groups by electrochemical reduction of aryl diazonium salts and then used as a cathode in MESs reactors. The results showed that the hydrophilicity of the carbon cloth surfaces improved after the carboxyl groups were modified. However, weaker current of cyclic voltammetry was obtained in the modified cathode. Significant differences were observed between modified (CA-H, CA-M, CA-L) and non-modified cathode (CK) during the start-up period. After 48h, the hydrogen production rate of CA-H, CA-M, CA-L was 21.45, 28.60, and 22.75 times higher than CK. After 120h, the acetate accumulation concentration of CA-H, CA-M, CA-L was 2.01, 2.43, and 1.44 times higher than CK. After 324h, there was little difference in the electrochemical activity of cathodic biofilm and protein content (about 0.47 mg·cm-2) in all groups. The analysis of the community structure of cathodic biofilm showed that, in the genus level, Acetobacterium, Norank_p_Saccharibacteria, and Thioclava were the dominant species, accounting for 59.6% to 82.1%. There was little difference in the relative abundance of Acetobacterium in all groups (31.3% to 40.1%). However, the relative abundance of norank_p_Saccharibacteria in CA-H, CA-M, CA-L, and CK were 16.1%, 24.6%, 31.1%, and 37.5%, respectively. The carboxyl modified cathode had a great influence on the start-up stage of MESs, which could be a new idea for the rapid start-up of MESs.

[Sulfate Reduction and Microbial Community of Autotrophic Biocathode in Response to Externally Applied Voltage].

The removal efficiencies of environmental pollutants in a microbial electrolysis system (MES) with a biocathode are highly affected by the externally applied voltage. Although the cathode biofilm plays a key role in the pollution removal, its response to the applied voltage is still unknown. A two-chambered MES with a biocathode was constructed to study the impact of the different applied voltages (0.4, 0.5, 0.6, 0.7, and 0.8 V) on the sulfate reduction, extracellular polymer formation, and cathodic bacterial community. The results show that the current output and coulomb and COD removals of the MES are positively correlated with the applied voltage ranging from 0.4 to 0.8 V. The sulfate reduction rate first increases and then decreases with increasing voltage in the MES. The maximum sulfate reductive rate[78.9 g·(m3·d)-1] and maximum S2- production (31.9 mg·L-1±2.2 mg·L-1) were achieved at 0.7 V. The highest electron recovery efficiencies of the MES are 41.8%; hydrogen production may be a pathway leading to electron loss. The polysaccharide and protein contents of the cathode biofilm increase with increasing voltage. The cathode biomass at 0.8 V is 70% higher than that at 0.4 V. The high throughput sequencing results show that Proteobacteria and Dsulfovibrio are dominant in the cathodic microbial community at the phylum and genus levels, respectively. The relative abundance of Desulfovibrio shows little variation with the increasing voltage, indicating that Desulfovibrio is of advantage for using the cathode as electron donor for the respiratory metabolism. With the increasing voltage, the distribution of Desulfovibrio at species level indicates that the changes of Desulfovibriox magneticus RS-1 and s_unclassified_g_Desulfovibrio are contrary.

Transcriptome Comparative Analysis of Salt Stress Responsiveness in Chrysanthemum (Dendranthema grandiflorum) Roots by Illumina- and Single-Molecule Real-Time-Based RNA Sequencing.

Salt response has long been considered a polygenic-controlled character in plants. Under salt stress conditions, plants respond by activating a great amount of proteins and enzymes. To develop a better understanding of the molecular mechanism and screen salt responsive genes in chrysanthemum under salt stress, we performed the RNA sequencing (RNA-seq) on both salt-processed chrysanthemum seedling roots and the control group, and gathered six cDNA databases eventually. Moreover, to overcome the Illumina HiSeq technology's limitation on sufficient length of reads and improve the quality and accuracy of the result, we combined Illumina HiSeq with single-molecule real-time sequencing (SMRT-seq) to decode the full-length transcripts. As a result, we successfully collected 550,823 unigenes, and from which we selected 48,396 differentially expressed genes (DEGs). Many of these DEGs were associated with the signal transduction, biofilm system, antioxidant system, and osmotic regulation system, such as mitogen-activated protein kinase (MAPK), Acyl-CoA thioesterase (ACOT), superoxide (SOD), catalase (CAT), peroxisomal membrane protein (PMP), and pyrroline-5-carboxylate reductase (P5CR). The quantitative real-time polymerase chain reaction (qRT-PCR) analysis of 15 unigenes was performed to test the data validity. The results were highly consistent with the RNA-seq results. In all, these findings could facilitate further detection of the responsive molecular mechanism under salt stress. They also provided more accurate candidate genes for genetic engineering on salt-tolerant chrysanthemums.

Transcriptome analysis of chrysanthemum (Dendranthema grandiflorum) in response to low temperature stress.

BACKGROUND: Chrysanthemum is one kind of ornamental plant well-known and widely used in the world. However, its quality and production were severely affected by low temperature conditions in winter and early spring periods. Therefore, we used the RNA-Seq platform to perform a de novo transcriptome assembly to analyze chrysanthemum (Dendranthema grandiflorum) transcription response to low temperature. RESULTS: Using Illumina sequencing technology, a total of 86,444,237 high-quality clean reads and 93,837 unigenes were generated from four libraries: T01, controls; T02, 4 °C cold acclimation (CA) for 24 h; T03, - 4 °C freezing treatments for 4 h with prior CA; and T04, - 4 °C freezing treatments for 4 h without prior CA. In total, 7583 differentially expressed genes (DEGs) of 36,462 annotated unigenes were identified. We performed GO and KEGG pathway enrichment analyses, and excavated a group of important cold-responsive genes related to low temperature sensing and signal transduction, membrane lipid stability, reactive oxygen species (ROS) scavenging and osmoregulation. These genes encode many key proteins in plant biological processes, such as protein kinases, transcription factors, fatty acid desaturase, lipid-transfer proteins, antifreeze proteins, antioxidase and soluble sugars synthetases. We also verified expression levels of 10 DEGs using quantitative real-time polymerase chain reaction (qRT-PCR). In addition, we performed the determination of physiological indicators of chrysanthemum treated at low temperature, and the results were basically consistent with molecular sequencing results. CONCLUSION: In summary, our study presents a genome-wide transcript profile of Dendranthema grandiflorum var. jinba and provides insights into the molecular mechanisms of D. grandiflorum in response to low temperature. These data contributes to our deeper relevant researches on cold tolerance and further exploring new candidate genes for chilling-tolerance and freezing-tolerance chrysanthemum molecular breeding.

Effect of Sevoflurane Anesthesia on Brain Is Mediated by lncRNA HOTAIR.

Postoperative cognitive dysfunction in elderly patients has been related to neurodegenerative disorders and mortality. Sevoflurane anesthesia has been implicated in both postoperative cognitive dysfunction and neurotoxicity. Given the advantages of using inhaled anesthetics like sevoflurane, it is important to understand how their usage results in neurotoxicity and subsequently devise ways to circumvent or attenuate the anesthetic-mediated induction in neurotoxicity. Long noncoding RNAs (LncRNAs) are a group of > 200 bp long RNAs and show specific spatiotemporal expression profiles. Several recent reports suggest that lncRNAs are involved in responses of the central nervous system (CNS) following acute injuries. However, their role in sevoflurane anesthesia-mediated cognitive dysfunction has not been studied. RNA immunoprecipitation (RIP) combined with qRT-PCR detection of six different lncRNAs showed that the HOTAIR lncRNAs were significantly more bound to both Sin3A and coREST, both corepressors of the RE-1 silencing transcription factor, within rat hippocampus following sevoflurane anesthesia compared with sham. Sevoflurane inhalation resulted in significant inhibition of brain-derived neurotrophic factor (BDNF) and cognitive impairment. Treatment with a combination of siRNAs targeting HOTAIR rescued BDNF expression and improved cognitive responses. Taken together, our results suggest that sevoflurane-mediated brain function impairment is at least in part mediated by the HOTAIR lncRNA.

Overexpression of a chrysanthemum transcription factor gene DgNAC1 improves the salinity tolerance in chrysanthemum.

KEY MESSAGE: DgNAC1, a transcription factor of chrysanthemum, was functionally verified to confer salt stress responses by regulating stress-responsive genes. NAC transcription factors play effective roles in resistance to different abiotic stresses, and overexpressions of NAC TFs in Arabidopsis have been proved to be conducive in improving salinity tolerance. However, functions of NAC genes in chrysanthemum continue to be poorly understood. Here, we performed physiology and molecular experiments to evaluate roles of DgNAC1 in chrysanthemum salt stress responses. In this study, DgNAC1-overexpressed chrysanthemum was obviously more resistant to salt over the WT (wild type). Specifically, the transgenic chrysanthemum showed a higher survival rate and lower EC (electrolyte conductivity) than WT under salt stress. The transgenic chrysanthemum also showed fewer accumulations of MDA (malondialdehyde) and reactive oxygen species (H2O2 and O2-), greater activities of SOD (superoxide dismutase), POD (peroxidase) and CAT (catalase), as well as more proline content than WT under salt stress. Furthermore, stress-responsive genes in transgenic chrysanthemum were greater up-regulated than in WT under salinity stress. Thus, all results revealed that DgNAC1 worked as a positive regulator in responses to salt stress and it may be an essential gene for molecular breeding of salt-tolerant plants.

Whole-transcriptome sequence analysis of differentially expressed genes in Phormium tenax under drought stress.

Phormium tenax is a kind of drought resistant garden plant with its rich and colorful leaves. To clarify the molecular mechanism of drought resistance in Phormium tenax, transcriptome was sequenced by the Illumina sequencing technology under normal and drought stress, respectively. A large number of contigs, transcripts and unigenes were obtained. Among them, only 30,814 unigenes were annotated by comparing with the protein databases. A total of 4,380 genes were differentially expressed, 2,698 of which were finally annotated under drought stress. Differentially expression analysis was also performed upon drought treatment. In KEGG pathway, the mechanism of drought resistance in Phormium tenax was explained from three aspects of metabolism and signaling of hormones, osmotic adjustment and reactive oxygen species metabolism. These results are helpful to understand the drought tolerance mechanism of Phormium tenax and will provide a precious genetic resource for drought-resistant vegetation breeding and research.

A modified oxic-settling-anaerobic activated sludge process using gravity thickening for excess sludge reduction.

Oxic-settling-anaerobic process (OSA) was known as a cost-effective way to reduce the excess sludge production with simple upgrade of conventional activated sludge process (CAS). A low oxidation-reduction potential (ORP) level was the key factor to sludge decay and lysis in the sludge holding tank of the OSA process. However, the ORP control with nitrogen purge or chemical dosing in the OSA process would induce extra expense and complicate the operation. Hence, in this study, a sludge holding tank using gravity thickening was applied to OSA process to reduce the excess sludge production without any ORP control. Results showed that the modified OSA process not only reduced the excess sludge production effectively but also improved the sludge settleability without affected the treatment capacity. The reduction of the excess sludge production in the modified OSA process resulted from interactions among lots of factors. The key element of the process was the gravity thickening sludge holding tank.

[Influence of substrate COD on methane production in single-chambered microbial electrolysis cell].

The chemical oxygen demand (COD) of substrate can affect the microbial activity of both anode and cathode biofilm in the single-chamber methanogenic microbial electrolysis cell (MEC). In order to investigate the effect of COD on the performance of MEC, a single chamber MEC was constructed with biocathode. With the change of initial concentration of COD (700, 1 000 and 1 350 mg x L(-1)), the methane production rate, COD removal and energy efficiency in the MEC were examined under different applied voltages. The results showed that the methane production rate and COD removal increased with the increasing COD. With the applied voltage changing from 0.3 to 0.7 V, the methane production rate increased at the COD of 700 mg x L(-1), while it increased at first and then decreased at the COD of 1000 mg x L(-1) and 1350 mg x L(-1). A similar trend was observed for the COD removal. The cathode potential reached the minimum (- 0.694 ± 0.001) V as the applied voltage was 0.5 V, which therefore facilitated the growth of methanogenic bacteria and improved the methane production rate and energy efficiency of the MEC. The maximum energy income was 0.44 kJ ± 0.09 kJ (1450 kJ x m(-3)) in the MEC, which was obtained at the initial COD of 1000 mg x L(-1) and the applied voltage of 0.5 V. Methanogenic MECs could be used for the treatment of wastewaters containing low organic concentrations to achieve positive energy production, which might provide a new method to recover energy from low-strength domestic wastewater.

[Characterization of biocatalysed sulfate reduction in a cathode of microbial electrolysis system].

In order to improve H2 utilization efficiency and to reduce energy consumption during the hydrogenotrophic sulfate reduction process, a two-chambered microbial electrolysis system (MES) with a biocathode was constructed. The performance of MES in terms of sulfate removal and the electron utilization was studied. With an applied voltage of 0.8 V, biocathode removed about 109.8 mg x L(-1) of SO4(2-) from the wastewater within 36 h of operation, and average reductive rate reached 73.2 mg x (L x d)(-1). The highest current density obtained from the MES was 50-60 A x m(-3). The total coulomb efficiency achieved in a cycle was (43.3 +/- 10.7)%, and around 90% of the effective electrons were used by the cathode bacteria for SO4(2-) reduction. During the operation of MES, the major products of SO4(2-) bio-reduction are sulfide and hydrogen sulfide. With an applied voltage of 0.4 V, both the SO4(2-) removal rate and electron output decreased compared with that of 0.8 V; however, the electric charge efficiency obtained by the MES increased and reached 70% when 0.4 V was applied. Meanwhile, ignorable H2 gas was detected at the end of the cycle, indicating bacteria might directly use cathode as the electron donor thus enhanced energy efficiency. The bacteria could use cathode of the MES as electron donor to reduce SO4(2-) effectively, which may provide a new method to lower energy consumption of the hydrogenotrophic sulfate reduction process, making advanced treatment for sulfate containing wastewater more affordable for practical applications.

Cloning and characterization of a novel vacuolar Na+/H+ antiporter gene (Dgnhx1) from chrysanthemum.

Plant vacuolar Na(+)/H(+) antiporter genes play significant roles in salt tolerance. However, the roles of the chrysanthemum vacuolar Na(+)/H(+) antiporter genes in salt stress response remain obscure. In this study, we isolated and characterized a novel vacuolar Na(+)/H(+) antiporter gene DgNHX1 from chrysanthemum. The DgNHX1 sequence contained 1920 bp with a complete open reading frame of 1533 bp encoding a putative protein of 510 amino acids with a predicted protein molecular weight of 56.3 kDa. DgNHX1 was predicted containing nine transmembrane domains. Its expression in the chrysanthemum was up-regulated by salt stress, but not by abscisic acid (ABA). To assess roles of DgNHX1 in plant salt stress responses, we performed gain-of-function experiment. The DgNHX1-overexpression tobacco plants showed significant salt tolerance than the wild type (WT). The transgenic lines exhibited more accumulation of Na(+) and K(+) under salt stress. These findings suggest that DgNHX1 plays a positive regulatory role in salt stress response.

A new oxic-settling-anaerobic (NOSA(®)) activated sludge process for minimizing excess sludge in secondary biological treatment plants: a pilot-scale evaluation of the absorption-biodegradation process.

This study compared the sludge reduction performance of a new oxic-settling-anaerobic (NOSA) process with that of a conventional adsorption-biodegradation process. A 50 m(3)/d pilot trial system with two different process configurations was operated for 6 months. The NOSA process functioned effectively in removing both chemical oxygen demand and nitrogen with the efficiencies of 86 and 92.5%, respectively, which reduced approximately 40% of the excess sludge. In this research, 0.77 kg volatile suspended solids/d sludge vanished in the anaerobic tank, which accounted for 58.9% of the total sludge loss in the NOSA process. Economic calculation suggests that the new process can dramatically upgrade the sludge reduction in wastewater treatment plants without a digestion device, and the investment for fundamental upgrading can be recovered in 5-6 years by cutting the costs of excess sludge dewatering and disposal treatment.

Overexpression of a novel chrysanthemum Cys2/His2-type zinc finger protein gene DgZFP3 confers drought tolerance in tobacco.

A drought stress-responsive Cys2/His2-type zinc finger protein gene DgZFP3 was previously isolated (Liu et al., Afr J Biotechnol 11:7781-7788, 2012b) from chrysanthemum. To assess roles of DgZFP3 in plant drought stress responses, we performed gain-of-function experiment. The DgZFP3-overexpression tobacco plants showed significant drought tolerance over the wild type (WT). The transgenic lines exhibited less accumulation of H2O2 under drought stress, more accumulation of proline and greater activities of peroxidase (POD) and superoxide dismutase than the WT under both control conditions and drought stress. In addition, there was greater up-regulation of the ROS-related enzyme genes (NtSOD and NtPOD) and stress-related genes (NtLEA5 and NtDREB) in transgenic lines under normal or drought conditons. Thus DgZFP3 probably plays a positive regulatory role in drought stress response and has the potential to be utilized in transgenic breeding to improve drought stress tolerance in plants.

Effects of aqueous extracts of Paeonia decomposita seeds on germination and some metabolic activities associated with growth of wheat seedlings.

Paeonia decomposita is a perennial deciduous shrub with great ornamental and medicinal values. Unfortunately, the distribution region, population size and individual numbers of P. decomposita rapidly decrease in the wild. It is a particularly rare, highly endangered, protective plant endemic to Southwest China. To understand the causes of seed dormancy of P. decomposita, the effects of aqueous extracts of the seed coat, endosperm of P. decomposita on germination, seedling growth and amylases activities of wheat seeds were examined in this paper. The results showed that the seed, especially the endosperm tissue of P. decomposita contained substances that strongly suppressed seed germination. The crude extract of endosperm of P. decomposita, which significantly reduced the activities of α and ß-amylase, showed a more significant inhibition than that of seed coat at the same dose. It was concluded that the presence of inhibitory substances in seed, especially in endosperm tissue, seem to be responsible for P. decomposita seed dormancy.

The evolution and utility of ribosomal ITS sequences in Bambusinae and related species: divergence, pseudogenes, and implications for phylogeny.

Ribosomal internal transcribed spacer (ITS) sequences are commonly used for phylogenetic reconstruction because they are highly reiterated as components of rDNA repeats, and hence are often subject to rapid homogenization through concerted evolution. Concerted evolution leads to intragenomic uniformity of repeats even between loci on nonhomologous chromosomes. However, a number of studies have shown that the ITS polymorphism within individuals is quite common. The molecular systematics of Bambusinae and related species were recently assessed by different teams using independently generated ITS sequences, and the results disagreed in some remarkable features. Here we compared the ITS sequences of the members of Bambusa s. l., the genera Dendrocalamus, Dinochloa, Gigantochloa, Guadua, Melocalamus, Monocladus, Oxytenanthera, Thyrsostachys, Pleioblastus, Pseudosasa and Schizostachyum.We have reanalysed the ITS sequences used by different research teams to reveal the underlying patterns of their different results. After excluding the sequences suspected to represent paralogous loci, a phylogenetic analysis of the subtribe Bambusinae species were performed using maximum parsimony and maximum-likelihood methods. The implications of the findings are discussed. The risk of incorporating ITS paralogues in plant evolutionary studies that can distort the phylogenetic signal should caution molecular systematists.

[Characterization of cross-linked quaternary chitosan salt and its adsorption of perchlorate from water].

Cross-linked quaternary chitosan salt was prepared and used to adsorb perchlorate from water. Parameters of cross-linking agent, temperature and pH were investigated to optimize the reaction conditions. The adsorption and regeneration ability of the adsorbent were also conducted. Quaternary chitosan salt could be fixed by cross-linking with glutaraldehyde using ethanol as dispersant. The optimal glutaraldehyde dosage and temperature were 6.82% and 45 degrees C, respectively. The cross-linked reaction was independent of pH with the range from 3 to 12. Quaternary chitosan salt was cross-linked mainly through the reaction between the methyl groups of ammonium on quaternary chitosan salt and the -C=O groups on glutaraldehyde. The optimal pH(zpc) of the adsorbent was about 10.6. The adsorbent showed high efficiency for perchlorate removal, and the adsorption capacity varied from 12.321 mg/g to 117.819 mg/g with the ClO4(-) concentration range from 5 mg/L to 200 mg/L. The spent adsorbents could be effectively regenerated by NaCl brine with the concentration more than 0.3%. The results suggest that the cross-linked chitosan quaternary ammonium salt would be a promising method for perchlorate removal from water.

Overexpression of a novel chrysanthemum NAC transcription factor gene enhances salt tolerance in tobacco.

The plant-specific NAC (for NAM, ATAF1, 2 and CUC2) transcription factors (TFs) have been implicated in different cellular processes involved in stress responses such as cold, high salinity or drought as well as abscisic acid (ABA) signalling. However, the roles of the chrysanthemum NAC TF genes in plant stress responses are still unclear. A full-length cDNA designated DgNAC1, containing a highly conserved N-terminal DNA-binding NAC domain, has been isolated from chrysanthemum by RACE (rapid amplification of cDNA ends). It encodes a protein of 284 amino acids residues (=~32.9 kDa) and theoretical pI of 7.13. The transcript of DgNAC1 was enriched in roots and flowers than in stems and leaves of the adult chrysanthemum plants. The gene expression was strongly induced by ABA, NaCl, drought and cold treatment in the seedlings. Subcellular localization revealed that DgNAC1:GFP fusion protein was preferentially distributed to nucleus. To assess whether DgNAC1 is a practically useful target gene for improving the stress tolerance of chrysanthemum, we ectopically over-expressed the full-length DgNAC1 cDNA in tobacco and found that the 35S:DgNAC1 transgenic tobacco exhibited a markedly increased tolerance to salt. Despite this increased salt stress tolerance, the transgenic tobacco showed no detectable phenotype defects under normal growth conditions. These results proposed that DgNAC1 is appropriate for application in genetic engineering strategies aimed at improving salt stress tolerance in chrysanthemum.

[Electricity generation and quinoline degradation of pure strains and mixed strains in the microbial fuel cell].

Microbial flora composition of microbial fuel cells (MFC) is important to the electricity generation. Four bacterium strains Q1, b, c and d which represent all different morphology of culturable bacterium were isolated from a MFC using 200 mg x L(-1) quinoline as the fuel and operating for at least 210 days. Strains Q1, c and d were Pseudomonas sp. based on 16S rDNA sequence analysis, while strain b was Burkholderia sp. Double-chamber MFCs using 200 mg x L(-1) quinoline and 300 mg x L(-1) glucose as the fuel and potassium ferricyanide as the electron acceptor were constructed. Results showed that strain b, c and d were non-electrogenesis. The electrical charges of MFC inoculated electrogenesis strain Q1 with non-electrogenesis strain b, c and d respectively were 3.00, 3.57 and 5.13C, and the columbic efficiency were 3.85%, 4.59% and 6.58%, which were all lower than that inoculated with pure Q1, because of the interspecific competition of electrogenesis and non-electrogenesis bacteria. Combinations of Q1 with the other three strains respectively resulted in 100% of quinoline degradation rates within 24h, which is better than pure cultures, that is, mixed microbial populations perform better in MFC when complex organics are used as the fuel. GC/MS analyses showed that only 2(1H)-quinolinone and phenol existed in the effluent of the MFC, which was inoculated with only Q1 or mixed bacteria.

[Power generation from glucose and nitrobenzene degradation using the microbial fuel cell].

By constructing a dual-chamber microbial fuel cell (MFC), experiments were carried out using an initial glucose concentration of 1 000 mg/L with different nitrobenzene (NB) concentrations (0, 50, 150 and 250 mg/L) as the MFC's fuel. Results showed that with an external resistance of 1 000 omega, the initial glucose concentration of 1 000 mg/L and the initial NB concentrations of 0, 50, 150, 250 mg/L, the operation periods were 55.7, 51.6, 45.9 and 32.2 h, respectively, the maximum voltage outputs were 670, 597, 507, and 489 mV, the maximum volumetric power densities were 28.57, 20.42, 9.29, and 8.47 W/m3, and the electric charges were 65.10, 43.50, 35.48, and 30.32 C. The MFC could use the NB and glucose mixtures as fuel and generated stable electricity outputs. The degradation rates of NB in the MFC in all cases reached up to 100% and COD removals in the MFC were 87% - 98%. However, the electricity generation was negligible when using 250 mg/L NB as the sole fuel. Denaturing gradient gel electrophoresis (DGGE) profiles demonstrated that the presence of NB resulted in changes of the dominant bacterial species on the electrodes.