30
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access
      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          By electronically wiring-up living cells with abiotic conductive surfaces, bioelectrochemical systems (BES) harvest energy and synthesize electric-/solar-chemicals with unmatched thermodynamic efficiency. However, the establishment of an efficient electronic interface between living cells and abiotic surfaces is hindered due to the requirement of extremely close contact and high interfacial area, which is quite challenging for cell and material engineering. Herein, we propose a new concept of a single cell electron collector, which is in-situ built with an interconnected intact conductive layer on and cross the individual cell membrane. The single cell electron collector forms intimate contact with the cellular electron transfer machinery and maximizes the interfacial area, achieving record-high interfacial electron transfer efficiency and BES performance. Thus, this single cell electron collector provides a superior tool to wire living cells with abiotic surfaces at the single-cell level and adds new dimensions for abiotic/biotic interface engineering.

          Abstract

          Efficient management of electron transfer between living cells and solid abiotic surfaces is quite challenging. Here, the authors report the assembling of single cell electron collector for individual cell to promote the biotic/abiotic interfacial electron transfer at the single-cell level.

          Related collections

          Most cited references49

          • Record: found
          • Abstract: found
          • Article: not found

          Extracellular electron transfer mechanisms between microorganisms and minerals.

          Electrons can be transferred from microorganisms to multivalent metal ions that are associated with minerals and vice versa. As the microbial cell envelope is neither physically permeable to minerals nor electrically conductive, microorganisms have evolved strategies to exchange electrons with extracellular minerals. In this Review, we discuss the molecular mechanisms that underlie the ability of microorganisms to exchange electrons, such as c-type cytochromes and microbial nanowires, with extracellular minerals and with microorganisms of the same or different species. Microorganisms that have extracellular electron transfer capability can be used for biotechnological applications, including bioremediation, biomining and the production of biofuels and nanomaterials.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Self-photosensitization of nonphotosynthetic bacteria for solar-to-chemical production.

            Improving natural photosynthesis can enable the sustainable production of chemicals. However, neither purely artificial nor purely biological approaches seem poised to realize the potential of solar-to-chemical synthesis. We developed a hybrid approach, whereby we combined the highly efficient light harvesting of inorganic semiconductors with the high specificity, low cost, and self-replication and -repair of biocatalysts. We induced the self-photosensitization of a nonphotosynthetic bacterium, Moorella thermoacetica, with cadmium sulfide nanoparticles, enabling the photosynthesis of acetic acid from carbon dioxide. Biologically precipitated cadmium sulfide nanoparticles served as the light harvester to sustain cellular metabolism. This self-augmented biological system selectively produced acetic acid continuously over several days of light-dark cycles at relatively high quantum yields, demonstrating a self-replicating route toward solar-to-chemical carbon dioxide reduction.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Macroporous and monolithic anode based on polyaniline hybridized three-dimensional graphene for high-performance microbial fuel cells.

              Microbial fuel cell (MFC) is of great interest as a promising green energy source to harvest electricity from various organic matters. However, low bacterial loading capacity and low extracellular electron transfer efficiency between the bacteria and the anode often limit the practical applications of MFC. In this work, a macroporous and monolithic MFC anode based on polyaniline hybridized three-dimensional (3D) graphene is demonstrated. It outperforms the planar carbon electrode because of its abilities to three-dimensionally interface with bacterial biofilm, facilitate electron transfer, and provide multiplexed and highly conductive pathways. This study adds a new dimension to the MFC anode design as well as to the emerging graphene applications. © 2012 American Chemical Society
                Bookmark

                Author and article information

                Contributors
                swd1978@ujs.edu.cn
                ycyong@ujs.edu.cn
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                14 August 2020
                14 August 2020
                2020
                : 11
                : 4087
                Affiliations
                [1 ]GRID grid.440785.a, ISNI 0000 0001 0743 511X, Biofuels Institute, School of Environment and Safety Engineering, , Jiangsu University, ; 301 Xuefu Road, Zhenjiang, 212013 China
                [2 ]GRID grid.440785.a, ISNI 0000 0001 0743 511X, School of Chemistry and Chemical Engineering, , Jiangsu University, ; 301 Xuefu Road, Zhenjiang, 212013 China
                Author information
                http://orcid.org/0000-0002-1660-1535
                http://orcid.org/0000-0003-1622-9638
                http://orcid.org/0000-0002-1123-8191
                http://orcid.org/0000-0003-1216-5163
                Article
                17897
                10.1038/s41467-020-17897-9
                7429851
                32796822
                e4bf1b29-b40b-43e4-880f-ea039dbe3066
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 29 December 2019
                : 22 July 2020
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                electrochemistry,electrocatalysis
                Uncategorized
                electrochemistry, electrocatalysis

                Comments

                Comment on this article