Cited by 128

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Influences of dissolved oxygen concentration on biocathodic microbial communities in microbial fuel cells

Rago, Laura, Cristiani, Pierangela, Villa, Federica, Zecchin, Sarah, Colombo, Alessandra, Cavalca, Lucia, Schievano, Andrea·2017·Bioelectrochemistry

Abstract

Dissolved oxygen (DO) at cathodic interface is a critical factor influencing microbial fuel cells (MFC) performance. In this work, three MFCs were operated with cathode under different DO conditions: i) air-breathing (A-MFC); ii) water-submerged (W-MFC) and iii) assisted by photosynthetic microorganisms (P-MFC). A plateau of maximum current was reached at 1.06±0.03mA, 1.48±0.06mA and 1.66±0.04mA, increasing respectively for W-MFC, P-MFC and A-MFC. Electrochemical and microbiological tools (Illumina sequencing, confocal microscopy and biofilm cryosectioning) were used to explore anodic and cathodic biofilm in each MFC type. In all cases, biocathodes improved oxygen reduction reaction (ORR) as compared to abiotic condition and A-MFC was the best performing system. Photosynthetic cultures in the cathodic chamber supplied high DO level, up to 16mg O2 L -1 , which sustained aerobic microbial community in P-MFC biocathode. Halomonas, Pseudomonas and other microaerophilic genera reached >50% of the total OTUs. The presence of sulfur reducing bacteria (Desulfuromonas) and purple non-sulfur bacteria in A-MFC biocathode suggested that the recirculation of sulfur compounds could shuttle electrons to sustain the reduction of oxygen as final electron acceptor. The low DO concentration limited the cathode in W-MFC. A model of two different possible microbial mechanisms is proposed which can drive predominantly cathodic ORR.

Overview

Integrity signals

Registry

Crossref · 10.1016/j.bioelechem.2017.04.001

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

Flagged first, then by citations

Research works printed but not linked: 75

  1. Kumar, 2013, Recent advances and challenges in the anode architecture and their modifications for the applications of microbial fuel cells, Biosens. Bioelectron., 43, 461, 10.1016/j.bios.2012.12.048 · DOI
  2. Kodali, 2017, High performance platinum group metal-free cathode catalysts for microbial fuel cell (MFC), J. Electrochem. Soc., 164, H3041, 10.1149/2.0061703jes · DOI
  3. Huang, 2011, Electron transfer mechanisms, new applications, and performance of biocathode microbial fuel cells, Bioresour. Technol., 102, 316, 10.1016/j.biortech.2010.06.096 · DOI
  4. Santini, 2015, Three-dimensional X-ray microcomputed tomography of carbonates and biofilm on operated cathode in single chamber microbial fuel cell, Biointerphases, 10, 31009, 10.1116/1.4930239 · DOI
  5. Cristiani, 2013, Cathodic and anodic biofilms in single chamber microbial fuel cells, Bioelectrochemistry, 92, 6, 10.1016/j.bioelechem.2013.01.005 · DOI
  6. Guerrini, 2014, Performance explorations of single chamber microbial fuel cells by using various microelectrodes applied to biocathodes, Int. J. Hydrog. Energy, 39, 21837, 10.1016/j.ijhydene.2014.06.132 · DOI
  7. Cristiani, 2013, Bacterial DGGE fingerprints of biofilms on electrodes of membraneless microbial fuel cells, Int. Biodeterior. Biodegrad., 84, 211, 10.1016/j.ibiod.2012.05.040 · DOI
  8. He, 2006, Application of bacterial biocathodes in microbial fuel cells, Electroanalysis, 18, 2009, 10.1002/elan.200603628 · DOI
  9. Rago, 2015, 2-Bromoethanesulfonate degradation in bioelectrochemical systems, Bioelectrochemistry, 105, 44, 10.1016/j.bioelechem.2015.05.001 · DOI
  10. Kim, 2007, Challenges in microbial fuel cell development and operation, Appl. Microbiol. Biotechnol., 76, 485, 10.1007/s00253-007-1027-4 · DOI
  11. He, 2015, Microbial fuel cells with an integrated spacer and separate anode and cathode modules, Environ. Sci. Water Res. Technol.
  12. Srikanth, 2016, Gas diffusion electrodes manufactured by casting evaluation as air cathodes for microbial fuel cells (MFC), Materials (Basel), 9, 601, 10.3390/ma9070601 · DOI
  13. Wu, 2014, Light intensity affects the performance of photo microbial fuel cells with Desmodesmus sp. A8 as cathodic microorganism, Appl. Energy, 116, 86, 10.1016/j.apenergy.2013.11.066 · DOI
  14. González Del Campo, 2013, Microbial fuel cell with an algae-assisted cathode: a preliminary assessment, J. Power Sources, 242, 638, 10.1016/j.jpowsour.2013.05.110 · DOI
  15. Gajda, 2013, Photosynthetic cathodes for microbial fuel cells, Int. J. Hydrog. Energy, 38, 11559, 10.1016/j.ijhydene.2013.02.111 · DOI
  16. Colombo, 2017, Assisting cultivation of photosynthetic microorganisms by microbial fuel cells to enhance nutrients recovery from wastewater, Bioresour. Technol., 10.1016/j.biortech.2017.03.038 · DOI
  17. Carvalho, 2006, Microalgal reactors: a review of enclosed system designs and performances, Biotechnol. Prog., 22, 1490, 10.1002/bp060065r · DOI
  18. Guerrini, 2013, Relation of anodic and cathodic performance to pH variations in membraneless microbial fuel cells, Int. J. Hydrog. Energy, 38, 345, 10.1016/j.ijhydene.2012.10.001 · DOI
  19. Santoro, 2014, Parameters characterization and optimization of activated carbon (AC) cathodes for microbial fuel cell application, Bioresour. Technol., 163, 54, 10.1016/j.biortech.2014.03.091 · DOI
  20. Chen, 1997, High cell density mixotrophic culture of Spirulina platensis on glucose for phycocyanin production using a fed-batch system, Enzym. Microb. Technol., 20, 221, 10.1016/S0141-0229(96)00116-0 · DOI
  21. Green, 2015, Deconstructing the polymerase chain reaction: understanding and correcting bias associated with primer degeneracies and primer-template mismatches, PLoS One, 10, e0128122, 10.1371/journal.pone.0128122 · DOI
  22. Bybee, 2011, Targeted amplicon sequencing (TAS): a scalable next-gen approach to multilocus, multitaxa phylogenetics, Genome Biol. Evol., 3, 1312, 10.1093/gbe/evr106 · DOI
  23. Moonsamy, 2013, High throughput HLA genotyping using 454 sequencing and the Fluidigm Access Array™ system for simplified amplicon library preparation, Tissue Antigens, 81, 141, 10.1111/tan.12071 · DOI
  24. Zhang, 2014, PEAR: a fast and accurate Illumina Paired-End reAd mergeR, Bioinformatics, 30, 614, 10.1093/bioinformatics/btt593 · DOI · Paper page
  25. Edgar, 2010, Search and clustering orders of magnitude faster than BLAST, Bioinformatics, 26, 2460, 10.1093/bioinformatics/btq461 · DOI
  26. Caporaso, 2010, QIIME allows analysis of high-throughput community sequencing data, Nat. Methods, 7, 335, 10.1038/nmeth.f.303 · DOI · Paper page
  27. Quast, 2013, The SILVA ribosomal RNA gene database project: improved data processing and web-based tools, Nucleic Acids Res., 41, D590, 10.1093/nar/gks1219 · DOI · Paper page
  28. Caporaso, 2010, PyNAST: a flexible tool for aligning sequences to a template alignment, Bioinformatics, 26, 266, 10.1093/bioinformatics/btp636 · DOI
  29. Hamady, 2009, Microbial community profiling for human microbiome projects: tools, techniques, and challenges, Genome Res., 19, 1141, 10.1101/gr.085464.108 · DOI
  30. Villa, 2012, Effects of chronic sub-lethal oxidative stress on biofilm formation by Azotobacter vinelandii, Biofouling, 28, 823, 10.1080/08927014.2012.715285 · DOI
  31. Villa, 2015, Development of a laboratory model of a phototroph-heterotroph mixed-species biofilm at the stone/air interface, Front. Microbiol., 6, 10.3389/fmicb.2015.01251 · DOI
  32. Mueller, 2006, Analysis of a marine phototrophic biofilm by confocal laser scanning microscopy using the new image quantification software PHLIP, BMC Ecol., 6, 1, 10.1186/1472-6785-6-1 · DOI
  33. Xavier, 2003, Automated biofilm morphology quantification from confocal laser scanning microscopy imaging, Water Sci. Technol., 47, 31, 10.2166/wst.2003.0273 · DOI
  34. Parameswaran, 2010, Microbial community structure in a biofilm anode fed with a fermentable substrate: the significance of hydrogen scavengers, Biotechnol. Bioeng., 105, 69, 10.1002/bit.22508 · DOI
  35. Logan, 2009, Exoelectrogenic bacteria that power microbial fuel cells, Nat. Rev. Microbiol., 7, 375, 10.1038/nrmicro2113 · DOI
  36. Rago, 2015, Microbial community analysis in a long-term membrane-less microbial electrolysis cell with hydrogen and methane production, Bioelectrochemistry, 106, 359, 10.1016/j.bioelechem.2015.06.003 · DOI
  37. Morita, 2011, Potential for Direct Interspecies Electron Transfer in Methanogenic, MBio, 10.1128/mBio.00159-11 · DOI
  38. Ishii, 2008, Comparison of electrode reduction activities of Geobacter sulfurreducens and an enriched consortium in an air-cathode microbial fuel cell, Appl. Environ. Microbiol., 74, 7348, 10.1128/AEM.01639-08 · DOI
  39. Heidrich, 2014, Performance of a pilot scale microbial electrolysis cell fed on domestic wastewater at ambient temperatures for a 12 month period, Bioresour. Technol., 173, 87, 10.1016/j.biortech.2014.09.083 · DOI
  40. Rabaey, 2004, Biofuel cells select for microbial consortia that self-mediate electron transfer, Appl. Environ. Microbiol., 70, 5373, 10.1128/AEM.70.9.5373-5382.2004 · DOI
  41. Chen, 2005, Proteiniphilum acetatigenes gen. nov., sp nov., from a UASB reactor treating brewery wastewater, Int. J. Syst. Evol. Microbiol., 55, 2257, 10.1099/ijs.0.63807-0 · DOI
  42. Montpart, 2015, Hydrogen production in single chamber microbial electrolysis cells with different complex substrates, Water Res., 68, 601, 10.1016/j.watres.2014.10.026 · DOI
  43. Montpart, 2014, Methanol opportunities for electricity and hydrogen production in bioelectrochemical systems, Int. J. Hydrog. Energy, 39, 770, 10.1016/j.ijhydene.2013.10.151 · DOI
  44. Zhao, 2014, Analysis of microbial community in a full-scale biogas digester of cold region using high-throughput sequencing technology, Harbin Gongye Daxue Xuebao/Journal Harbin Inst. Technol., 46
  45. Liang, 2015, Anaerolineaceae and Methanosaeta turned to be the dominant microorganisms in alkanes-dependent methanogenic culture after long-term of incubation, AMB Express, 5, 37, 10.1186/s13568-015-0117-4 · DOI
  46. Strompl, 2003, Oceanicaulis alexandrii gen. nov., sp. nov., a novel stalked bacterium isolated from a culture of the dinoflagellate Alexandrium tamarense (Lebour) Balech, Int. J. Syst. Evol. Microbiol., 53, 1901, 10.1099/ijs.0.02635-0 · DOI
  47. Bowman, 2015, Family III. Cryomorphaceae Bergey's manual of systematic bacteriology, vol. 4, 322
  48. Lau, 2005, Owenweeksia hongkongensis gen. nov., sp. nov., a novel marine bacterium of the phylum “Bacteroidetes”, Int. J. Syst. Evol. Microbiol., 55, 1051, 10.1099/ijs.0.63155-0 · DOI
  49. Zheng, 2014, Bacterial community structure and its regulating factors in the intertidal sediment along the Liaodong Bay of Bohai Sea, China, Microbiol. Res., 169, 585, 10.1016/j.micres.2013.09.019 · DOI
  50. Mnif, 2009, Isolation and characterization of Halomonas sp. strain C2SS100, a hydrocarbon-degrading bacterium under hypersaline conditions, J. Appl. Microbiol., 107, 785, 10.1111/j.1365-2672.2009.04251.x · DOI
  51. Sorokin, 2000, Roseinatronobacter thiooxidans Gen. Nov., sp. Nov., a new alkaliphilic aerobic bacteriochlorophyll-alpha-containing bacteria from a soda lake, Mikrobiologiia, 59, 89
  52. Saunders, 1978, Genetics of Rhodospirillaceae, Microbiol. Rev., 42, 357, 10.1128/MMBR.42.2.357-384.1978 · DOI
  53. Franzetti, 2017, Monod kinetics degradation of low concentration residual organics in membraneless microbial fuel cells, J. Electrochem. Soc., 164, H3091, 10.1149/2.0141703jes · DOI
  54. Kurata, 2007, Alkalimonas collagenimarina sp. nov., a psychrotolerant, obligate alkaliphile isolated from deep-sea sediment, Int. J. Syst. Evol. Microbiol., 57, 1549, 10.1099/ijs.0.65084-0 · DOI
  55. Ma, 2004, Alkalimonas amylolytica gen. nov., sp. nov., and Alkalimonas delamerensis gen. nov., sp. nov., novel alkaliphilic bacteria from soda lakes in China and East Africa, Extremophiles, 8, 193, 10.1007/s00792-004-0377-4 · DOI
  56. Reinholdhurek, 1993, Azoarcus gen-nov, nitrogen-fixing proteobacteria associated with roots of kallar grass (Leptochloa-Fusca (L) Kunth), and description of 2 species, Azoarcus-indigens sp-nov and Azoarcus-communis sp-nov, Int. J. Syst. Bacteriol., 43, 574, 10.1099/00207713-43-3-574 · DOI
  57. Springer, 1998, Azoarcus anaerobius sp. nov., a resorcinol-degrading, strictly anaerobic, denitrifying bacterium, Int. J. Syst. Bacteriol., 48, 953, 10.1099/00207713-48-3-953 · DOI
  58. Peix, 2009, Historical evolution and current status of the taxonomy of genus Pseudomonas, Infect. Genet. Evol., 9, 1132, 10.1016/j.meegid.2009.08.001 · DOI
  59. Stackebrandt, 2006, The genus Erysipelothrix, vol. 4, 492
  60. Borole, 2011, Electroactive biofilms: current status and future research needs, Energy Environ. Sci., 4, 4813, 10.1039/c1ee02511b · DOI
  61. Finkenstadt, 2005, Natural polysaccharides as electroactive polymers, Appl. Microbiol. Biotechnol., 67, 735, 10.1007/s00253-005-1931-4 · DOI
  62. Guarino, 2016, Electro-active polymers (EAPs): a promising route to design bio-organic/bioinspired platforms with on demand functionalities, Polymers (Basel), 8, 185, 10.3390/polym8050185 · DOI
  63. Li, 2016, Redox properties of extracellular polymeric substances (EPS) from electroactive bacteria, Sci. Rep., 6, 39098, 10.1038/srep39098 · DOI
  64. Steidl, 2016, Mechanistic stratification in electroactive biofilms of Geobacter sulfurreducens mediated by pilus nanowires, Nat. Commun., 7, 12217, 10.1038/ncomms12217 · DOI
  65. Flemming, 2010, The biofilm matrix, Nat. Rev. Microbiol., 10.1038/nrmicro2415 · DOI · Paper page
  66. Carvalho, 2014, The study of marine corrosion of copper alloys in chlorinated condenser cooling circuits: the role of microbiological components, Bioelectrochemistry, 97, 2, 10.1016/j.bioelechem.2013.12.005 · DOI
  67. Kamata, 2014, Spirulina-templated metal microcoils with controlled helical structures for THz electromagnetic responses, Sci. Rep., 4, 4919, 10.1038/srep04919 · DOI
  68. Wang, 2005, Morphological reversion of Spirulina (Arthrospira) platensis (Cyanophyta): from linear to helical, J. Phycol., 41, 622, 10.1111/j.1529-8817.2005.00087.x · DOI
  69. Hongsthong, 2007, Revealing differentially expressed proteins in two morphological forms of Spirulina platensis by proteomic analysis, Mol. Biotechnol., 36, 123, 10.1007/s12033-007-0013-5 · DOI
  70. Gajda, 2015, Self-sustainable electricity production from algae grown in a microbial fuel cell system, Biomass Bioenergy, 82, 87, 10.1016/j.biombioe.2015.05.017 · DOI
  71. Stewart, 2008, Physiological heterogeneity in biofilms, Nat. Rev. Microbiol., 6, 199, 10.1038/nrmicro1838 · DOI
  72. Behera, 2010, Performance evaluation of low cost microbial fuel cell fabricated using earthen pot with biotic and abiotic cathode, Bioresour. Technol., 101, 1183, 10.1016/j.biortech.2009.07.089 · DOI
  73. Sun, 2011, Electricity generation and microbial community changes in microbial fuel cells packed with different anodic materials, Bioresour. Technol., 102, 10886, 10.1016/j.biortech.2011.09.038 · DOI
  74. Ghosh, 2009, Biochemistry and molecular biology of lithotrophic sulfur oxidation by taxonomically and ecologically diverse bacteria and archaea, FEMS Microbiol. Rev., 33, 999, 10.1111/j.1574-6976.2009.00187.x · DOI
  75. Zhang, 2008, Chemical and biological technologies for hydrogen sulfide emission control in sewer systems: a review, Water Res., 42, 1, 10.1016/j.watres.2007.07.013 · DOI

Cited by

Sorted by citations

Metadata

Authors
Rago, L., Cristiani, P., Villa, F., Zecchin, S., Colombo, A., Cavalca, L., & Schievano, A.
Venue
Bioelectrochemistry
Publisher
Elsevier BV
Published
2017-08
Volume
116
Pages
39-51
ISSN
1567-5394
Cited by
128
References
1
Language
en
Funders
  • MIUR (RBSI14JKU3)
  • Research Fund for the Italian Electrical System

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review