Biofuel Cells. Группа авторов

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СКАЧАТЬ Bunte, C., Prucker, O., Konig, T., Ruhe, J., Enzyme Containing Redox Polymer Networks for Biosensors or Biofuel Cells: A Photochemical Approach. Langmuir, 26, 6019–6027, 2010.

      45. Meredith, S., Xu, S., Meredith, M.T., Minteer, S.D., Hydrophobic Saltmodified Nafion for Enzyme Immobilization and Stabilization. JoVE, e3949, 2012.

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48. Calvo, E.J., Etchenique, R., Pietrasanta, L., Wolosiuk, A., Danilowicz, C., Layer-By-Layer Self-Assembly of Glucose Oxidase and Os(Bpy)₂ClPyCH2NH−poly(Allylamine) Bioelectrode. Anal. Chem., 73, 1161–1168, 2001.

      49. El Ichi-Ribault, S., Zebda, A., Tingry, S., Petit, M., et al., Performance and stability of chitosan-MWCNTs-laccase biocathode: Effect of MWCNTs surface charges and ionic strength. J.Electroanal. Chem., 799, 26–33, 2017.

      50. Rengaraj, S., Mani, V., Kavanagh, P., Rusling, J., Leech, D., A membrane-less enzymatic fuel cell with layer-by-layer assembly of redox polymer and enzyme over graphite electrodes. Chem. Commun., 47, 11861–11863, 2011.

      51. Meredith, M.T., Kao, D.-Y., Hickey, D., Schmidtke, D.W., Glatzhofer, D.T., High Current Density Ferrocene-Modified Linear Poly(ethylenimine) Bioanodes and Their Use in Biofuel Cells. J. Electrochem. Soc., 158, B166–B174, 2011.

      52. Dunn, B., Lan, E., Design of Biohybrid Structures for Enzyme–Electrode Interfaces, Hybrid Organic.–Inorganic Interfaces, pp. 767–791, John Wiley & Sons, Ltd, 2017.

      53. Christwardana, M., Kim, K.J., Kwon, Y., Fabrication of Mediatorless/Membraneless Glucose/Oxygen Based Biofuel Cell using Biocatalysts Including Glucose Oxidase and Laccase Enzymes. Sci. Reports, 6, 30128, 2016.

      54. Díaz-González, J.-c. M., Escalona-Villalpando, R.A., Arriaga, L.G., Minteer, S.D., Casanova-Moreno, J.R., Effects of the cross-linker on the performance and stability of enzymatic electrocatalytic films of glucose oxidase and dimethylferrocene-modified linear poly(ethyleneimine). Electrochim. Acta, 337, 135782, 2020.

      55. Oztekin, Y., Krikstolaityte, V., Ramanaviciene, A., Yazicigil, Z., Ramanavicius, A., 1,10-Phenanthroline derivatives as mediators for glucose oxidase. Biosens. Bioelectron., 26, 267–270, 2010.

      56. MacAodha, D., Ferrer, M.L., Conghaile, P.Ó., Kavanagh, P., Leech, D., Crosslinked redox polymer enzyme electrodes containing carbon nanotubes for high and stable glucose oxidation current. Phys. Chem. Chem. Phys., 14, 14667–14672, 2012.

      57. Kobayashi, S., Hiroishi, K., Tokunoh, M., Saegusa, T., Chelating properties of linear and branched poly(ethylenimines). Macromol., 20, 1496–1500, 1987.

      58. Chung, Y., Hyun, K.H., Kwon, Y., Fabrication of a biofuel cell improved by the π-conjugated electron pathway effect induced from a new enzyme catalyst employing terephthalaldehyde. Nanoscale, 8, 1161–1168, 2016.

      59. Chung, Y., Christwardana, M., Tannia, D.C., Kim, K.J., Kwon, Y., Biocatalyst including porous enzyme cluster composite immobilized by two-step cross-linking and its utilization as enzymatic biofuel cell. J. Power Sources, 360, 172–179, 2017.

      60. Castelli, F., Pitarresi, G., Giammona, G., Influence of different parameters on drug release from hydrogel systems to a biomembrane model. Evaluation by differential scanning calorimetry technique. Biomater., 21, 821–833, 2000.

61. Speit, G., Neuss, S., Schütz, P., Fröhler-Keller, M., Schmid, O., The genotoxic potential of glutaraldehyde in mammalian cells in vitro in comparison with formaldehyde. Mutat. Res./Genetic Toxicol. Environ. Mutagen., 649, 146–154, 2008.

      62. Vasylieva, N., Barnych, B., Meiller, A., Maucler, C., et al., Covalent enzyme immobilization by poly(ethylene glycol) diglycidyl ether (PEGDE) for microelectrode biosensor preparation. Biosens. Bioelectron., 26, 3993–4000, 2011.

      63. Meredith, M.T., Hickey, D.P., Redemann, J.P., Schmidtke, D.W., Glatzhofer, D.T., Effects of ferrocene methylation on ferrocene-modified linear poly(ethylenimine) bioanodes. Electrochim. Acta, 92, 226–235, 2013.

      64. Hickey, D.P., Halmes, A.J., Schmidtke, D.W., Glatzhofer, D.T., Electrochemical Characterization of Glucose Bioanodes Based on Tetramethylferrocene-Modified Linear Poly(ethylenimine). Electrochim. Acta, 149, 252–257, 2014.

      65. Chen, J., Munje, R., Godman, N.P., Prasad, S., et al., Improved Performance of Glucose Bioanodes Using Composites of (7,6) Single-Walled Carbon Nanotubes and a Ferrocene-LPEI Redox Polymer. Langmuir, 33, 7591–7599, 2017.

      66. Conghaile, P.O., Kamireddy, S., MacAodha, D., Kavanagh, P., Leech, D., Mediated glucose enzyme electrodes by cross-linking films of osmium redox complexes and glucose oxidase on electrodes. Anal. Bioanal. Chem., 405, 3807–3812, 2013.

      67. Chabert, N., Ali, O.A., Achouak, W., All ecosystems potentially host electrogenic bacteria. Bioelectrochem., 106, 88–96, 2015.

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      69. Cercado-Quezada, B., Delia, M.L., Bergel, A., Testing various food-industry wastes for electricity production in microbial fuel cell. Bioresour. Technol., 101, 2748–2754, 2010.

      70. Cercado, B., Byrne, N., Bertrand, M., Pocaznoi, D., et al., Garden compost inoculum leads to microbial bioanodes with potential-independent characteristics. Bioresour. Technol., 134, 276–284, 2013.

      71. Shi, M.M., Jiang, Y.G., Shi, L., Electromicrobiology and biotechnological applications of the exoelectrogens Geobacter and Shewanella spp. Sci. China-Technological Sci., 62, 1670–1678, 2019.

      72. Thirumurthy, M.A., Jones, A.K., Geobacter cytochrome OmcZs binds riboflavin: Implications for extracellular electron transfer. Nanotechnol., 31, 2020.

      73. Lovley, D.R., Walker, D.J.F., Geobacter Protein Nanowires. Front. Microbiol., 10, 2019.

      74. Marsili, E., Baron, D.B., Shikhare, I.D., Coursolle, D., et al., Shewanella Secretes flavins that mediate extracellular electron transfer. PNAS USA, 105, 3968–3973, 2008.

75. Cheng, Z.H., Xiong, J.R., Min, D., Cheng, L., et al., Promoting bidirectional extracellular electron transfer of Shewanella oneidensis MR-1 for hexavalent chromium reduction via elevating intracellular cAMP level. Biotechnol. Bioeng. http://doi.org/10.1002/bit.27305, 2020.

      76. Engel, C., Schattenberg, F., Dohnt, K., Schroder, U., et al., Long-Term Behavior of Defined Mixed Cultures of Geobacter sulfurreducens and Shewanella oneidensis in Bioelectrochemical Systems. Front. Bioeng. Biotechnol., 7, 2019.

      77. Li, Y.R., Wen, L.L., Zhao, H.P., Zhu, L.Z., Addition of Shewanella СКАЧАТЬ