12
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Lack of Periplasmic Non-heme Protein SorA Increases Shewanella decolorationis Current Generation

      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

          Bacterial extracellular electron transport (EET) plays an important role in many natural and engineering processes. Some periplasmic non-heme redox proteins usually coexist with c-type cytochromes (CTCs) during the EET process. However, in contrast to CTCs, little is known about the roles of these non-heme redox proteins in EET. In this study, the transcriptome of Shewanella decolorationis S12 showed that the gene encoding a periplasmic sulfite dehydrogenase molybdenum-binding subunit SorA was significantly up-regulated during electrode respiration in microbial fuel cells (MFCs) compared with that during azo-dye reduction. The maximum current density of MFCs catalyzed by a mutant strain lacking SorA (Δ sorA) was 25% higher than that of wild strain S12 (20 vs. 16 μA/cm 2). Both biofilm formation and the current generation of the anodic biofilms were increased by the disruption of sorA, which suggests that the existence of SorA in S. decolorationis S12 inhibits electrode respiration. In contrast, disruption of sorA had no effect on respiration by S. decolorationis S12 with oxygen, fumarate, azo dye, or ferric citrate as electron acceptors. This is the first report of the specific effect of a periplasmic non-heme redox protein on EET to electrode and provides novel information for enhancing bacterial current generation.

          Related collections

          Most cited references33

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

          Extracellular electron transfer via microbial nanowires.

          Microbes that can transfer electrons to extracellular electron acceptors, such as Fe(iii) oxides, are important in organic matter degradation and nutrient cycling in soils and sediments. Previous investigations on electron transfer to Fe(iii) have focused on the role of outer-membrane c-type cytochromes. However, some Fe(iii) reducers lack c-cytochromes. Geobacter species, which are the predominant Fe(iii) reducers in many environments, must directly contact Fe(iii) oxides to reduce them, and produce monolateral pili that were proposed, on the basis of the role of pili in other organisms, to aid in establishing contact with the Fe(iii) oxides. Here we report that a pilus-deficient mutant of Geobacter sulfurreducens could not reduce Fe(iii) oxides but could attach to them. Conducting-probe atomic force microscopy revealed that the pili were highly conductive. These results indicate that the pili of G. sulfurreducens might serve as biological nanowires, transferring electrons from the cell surface to the surface of Fe(iii) oxides. Electron transfer through pili indicates possibilities for other unique cell-surface and cell-cell interactions, and for bioengineering of novel conductive materials.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Direct exchange of electrons within aggregates of an evolved syntrophic coculture of anaerobic bacteria.

            Microbial consortia that cooperatively exchange electrons play a key role in the anaerobic processing of organic matter. Interspecies hydrogen transfer is a well-documented strategy for electron exchange in dispersed laboratory cultures, but cooperative partners in natural environments often form multispecies aggregates. We found that laboratory evolution of a coculture of Geobacter metallireducens and Geobacter sulfurreducens metabolizing ethanol favored the formation of aggregates that were electrically conductive. Sequencing aggregate DNA revealed selection for a mutation that enhances the production of a c-type cytochrome involved in extracellular electron transfer and accelerates the formation of aggregates. Aggregate formation was also much faster in mutants that were deficient in interspecies hydrogen transfer, further suggesting direct interspecies electron transfer.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Structure of Microbial Nanowires Reveals Stacked Hemes that Transport Electrons over Micrometers

              Long-range (>10 μm) transport of electrons along networks of Geobacter sulfurreducens protein filaments, known as microbial nanowires, has been invoked to explain a wide range of globally important redox phenomena. These nanowires were previously thought to be type IV pili composed of PilA protein. Here we report a 3.7 Å resolution cryo-electron microscopy structure which surprisingly reveals that, rather than PilA, G. sulfurreducens nanowires are assembled by micrometer-long polymerization of the hexaheme cytochrome OmcS, with hemes packed within ~3.5–6 Å of each other. The inter-subunit interfaces show unique structural elements such as inter-subunit parallel-stacked hemes and axial coordination of heme by histidines from neighbouring subunits. Wild-type OmcS filaments show 100-fold greater conductivity than other filaments from an Δ omcS strain, highlighting the importance of OmcS to conductivity in these nanowires. This structure explains the remarkable capacity of soil bacteria to transport electrons to remote electron acceptors for respiration and energy sharing.
                Bookmark

                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                25 February 2020
                2020
                : 11
                : 262
                Affiliations
                [1] 1School of Biology and Biological Engineering, South China University of Technology , Guangzhou, China
                [2] 2Guangdong Institute of Microbiology, Guangdong Academy of Sciences , Guangzhou, China
                [3] 3State Key Laboratory of Applied Microbiology Southern China , Guangzhou, China
                [4] 4College of Food Science and Technology, Henan University of Technology , Zhengzhou, China
                [5] 5Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application , Guangzhou, China
                Author notes

                Edited by: Amelia-Elena Rotaru, University of Southern Denmark, Denmark

                Reviewed by: Johannes Gescher, Karlsruhe Institute of Technology (KIT), Germany; Catarina Paquete, New University of Lisbon, Portugal

                *Correspondence: Yonggang Yang, yyg117@ 123456163.com

                This article was submitted to Microbiological Chemistry and Geomicrobiology, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2020.00262
                7052111
                32158435
                6c79fe6d-08e5-4761-9207-7adc99933a83
                Copyright © 2020 Kong, Song, Guo, Sun, Zhu, Chen, Yang and Xu.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 15 September 2019
                : 04 February 2020
                Page count
                Figures: 4, Tables: 1, Equations: 0, References: 39, Pages: 9, Words: 0
                Funding
                Funded by: National Natural Science Foundation of China 10.13039/501100001809
                Award ID: 91851202
                Award ID: 51678163
                Award ID: U1701243
                Funded by: Natural Science Foundation of Guangdong Province 10.13039/501100003453
                Award ID: 2016A030306021
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                extracellular electron transport,molybdenum-binding protein,sora,current generation,biofilm

                Comments

                Comment on this article