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Isolation, Identification and Characteristic Analysis of Plant Endophyte Electrogenic Bacteria Shinella zoogloeoides SHE10

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Abstract

Electroactive microorganisms play a significant role in microbial fuel cells (MFCs). These devices are environmentally friendly and can turn large quantities of organic material into renewable energy based on microbial diversity. Based on broad microbial diversity, it is necessary to obtain a comprehensive understanding of their resource distribution and to discover potential resources. In this study, sweet potato tissues were selected to isolate endophytic bacteria, and the electrochemical activity potential of those bacteria was evaluated by high-throughput screening with a WO3 nanoprobe. This study was screened and obtained a strain SHE10 with electrochemical performance from the rhizome of sweet potato by a WO3 nanoprobe, which was identified as Shinella zoogloeoides. After nearly 600 h of voltage monitoring and cyclic voltammetry analysis, the results showed that the average voltage of S. zoogloeoides SHE10 reached 122.5 mV in stationary period. The maximum power density is 78.3 ± 1.8 mW/m2, and the corresponding current density is 223.0 mA/m2. The good redox reaction also indicated that the strain had good electrical activity. Its electron transfer mode was diverse, but its power generation mechanism still needs to be further discussed. The study of S. zoogloeoides SHE10 provides scientific theoretical reference for expanding the resource pool of electroproducing bacteria and the types of electroproducing microorganisms.

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References

  1. Allen RM, Bennetto HP (1993) Microbial fuel-cells - Electricity production from carbohydrates. Appl Biochem Biotechnol 39:27–40. https://doi.org/10.1007/BF02918975

    Article  Google Scholar 

  2. Lovley DR (2008) The microbe electric: conversion of organic matter to electricity. Curr Opin Biotechnol 19:564–571. https://doi.org/10.1016/j.copbio.2008.10.005

    Article  CAS  PubMed  Google Scholar 

  3. Fan Y, Han SK, Liu H (2012) Improved performance of CEA microbial fuel cells with increased reactor size. Energy Environ Sci 5:8273–8280. https://doi.org/10.1039/C2EE21964F

    Article  CAS  Google Scholar 

  4. Chen WW, Liu ZL, Li YX (2021) Improved electricity generation, coulombic efficiency and microbial community structure of microbial fuel cells using sodium citrate as an effective additive. J Power Sources 482:228947. https://doi.org/10.1016/j.jpowsour.2020.228947

    Article  CAS  Google Scholar 

  5. Rossi R, Hur AY, Page MA (2022) Pilot scale microbial fuel cells using air cathodes for producing electricity while treating wastewater. Water Res 215:118208. https://doi.org/10.1016/j.watres.2022.118208

    Article  CAS  PubMed  Google Scholar 

  6. Zhang J, Chen RY, Du C (2021) Effects of continuous sulfamonomethoxine shock on the power generation performance and microbial community structure of MFCs under seasonal temperature variation. Biochem Eng J 167:107909. https://doi.org/10.1016/j.bej.2020.107909

    Article  CAS  Google Scholar 

  7. Shen J, Li JF, Li FS (2021) Effect of lignite activated coke packing on power generation and phenol degradation in microbial fuel cell treating high strength phenolic wastewater. Chemical Engineering Journa 417:128091. https://doi.org/10.1016/j.cej.2020.128091

    Article  CAS  Google Scholar 

  8. Chauhan S, Sharma V, Varjani S (2022) Mitigation of tannery effluent with simultaneous generation of bioenergy using dual chambered microbial fuel cell. Biores Technol 351:127084. https://doi.org/10.1016/j.biortech.2022.127084

    Article  CAS  Google Scholar 

  9. Li M, Zhou MH, Tian XY (2018) Microbial fuel cell (MFC) power performance improvement through enhanced microbial electrogenicity. Biotechnol Adv 36:1316–1327. https://doi.org/10.1016/j.biotechadv.2018.04.010

    Article  CAS  PubMed  Google Scholar 

  10. Yuan SJ, He H, Sheng GP (2013) A photometric high-throughput method for identification of electrochemically active bacteria using a WO 3 nanocluster probe. Sci Rep 3:1–7. https://doi.org/10.1038/srep01315

    Article  CAS  Google Scholar 

  11. Ling LJ, Li ZB, Yang CY (2020) Plant endophytic bacteria: a potential resource pool of electroactive microorganisms. Biorxiv 10:334912. https://doi.org/10.1101/2020.10.11.334912

    Article  Google Scholar 

  12. Da Silva P, Nahas E (2002) Bacterial diversity in soil in response to different plants, phosphate fertilizers and liming. Brazilian J Microbiol 33:304–310. https://doi.org/10.1590/S1517-83822002000400005

    Article  Google Scholar 

  13. Widdel F, Bak F (1992) Gram-negative mesophilic sulfate-reducing bacteria. In: The Prokaryotes. Springer New York, pp 3352–3378 https://doi.org/10.1007/978-1-4757-2191-1_21

  14. Dudley K (1990) Short protocols in molecular biology. FEBS Lett 268:434–434. https://doi.org/10.1016/S0960-0760(97)80799-6

    Article  Google Scholar 

  15. Ling LJ, Yang CY, Ma WX (2020) Isolation, identification and control of a resistant bacterium strain found in Ku shui rose pure dew. J Food Process Preserv 45:15061. https://doi.org/10.1111/jfpp.15061

    Article  CAS  Google Scholar 

  16. Schloss PD, Westcott SL (2011) Assessing and improving methods used in operational taxonomic unit-based approaches for 16S rRNA gene sequence analysis. Appl Environ Microbiol 77:3219–3226. https://doi.org/10.1128/AEM.02810-10

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Kimura M (1980) A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 16:111–120. https://doi.org/10.1007/BF01731581

    Article  CAS  PubMed  Google Scholar 

  18. Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4:406–425

    CAS  PubMed  Google Scholar 

  19. Felsenstein J (1985) Confidence limits on phylogenies: an approach using the bootstrap. Evolution (N Y) 39:783–791. https://doi.org/10.1111/j.1558-5646.1985.tb00420.x

    Article  Google Scholar 

  20. Bond DR, Lovley DR (2003) Electricity production by Geobacter sulfurreducens attached to electrodes. Appl Environ Microbiol 69:1548–1555. https://doi.org/10.1128/AEM.69.3.1548-1555.2003

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Logan B, Cheng S, Watson V, Estadt G (2007) Graphite fiber brush anodes for increased power production in air-cathode microbial fuel cells. Environ Sci Technol 41:3341–3346. https://doi.org/10.1021/es062644y

    Article  CAS  PubMed  Google Scholar 

  22. Xia X, Cao XX, Liang P (2010) Electricity generation from glucose by a Klebsiella sp. in microbial fuel cells. Appl Microbiol Biotechnol 87:383–390. https://doi.org/10.1007/s00253-010-2604-5

    Article  CAS  PubMed  Google Scholar 

  23. Bowon K (1999) Dynamic effects of learning capabilities and profit structures on the innovation competition. Optim Control Appl Methods 20:127–144. https://doi.org/10.1002/(SICI)1099-1514(199905/06)20:3%3c127::AID-OCA650%3e3.0.CO;2-I

    Article  Google Scholar 

  24. Kim BH, Ikeda T, Park HS (1999) Electrochemical activity of an Fe ( III ) -reducing bacterium, Shewanella putrefaciens IR-1, in the presence of alternative electron acceptors. Biotechnol Tech 200:475–478. https://doi.org/10.1023/A:1008993029309

    Article  Google Scholar 

  25. Marsili E, Baron DB, Shikhare ID (2008) Shewanella secretes flavins that mediate extracellular electron transfer. Proc Natl Acad Sci U S A 105:3968–3973. https://doi.org/10.1073/pnas.0710525105

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Call DF, Logan BE (2011) A method for high throughput bioelectrochemical research based on small scale microbial electrolysis cells. Biosens Bioelectron 26:4526–4531. https://doi.org/10.1016/j.bios.2011.05.014

    Article  CAS  PubMed  Google Scholar 

  27. Harrison JG, Griffin EA (2020) The diversity and distribution of endophytes across biomes, plant phylogeny and host tissues: how far have we come and where do we go from here? Environ Microbiol 22:2107–2123. https://doi.org/10.1111/1462-2920.14968

    Article  PubMed  PubMed Central  Google Scholar 

  28. Mao L, Verwoerd WS (2013) Selection of organisms for systems biology study of microbial electricity generation: a review. Int J Energy Environ Eng 4:1–18. https://doi.org/10.1186/2251-6832-4-17

    Article  CAS  Google Scholar 

  29. Zekker I, Bhowmick GD, Priks H (2020) ANAMMOX-denitrification biomass in microbial fuel cell to enhance the electricity generation and nitrogen removal efficienc. Biodegradation 31:249–264. https://doi.org/10.1007/s10532-020-09907-w

    Article  CAS  PubMed  Google Scholar 

  30. Jssa B, Raunija TSK, Verma A (2021) Impregnated thermoset pre-pressurized carbon composite electrodes in microbial fuel cell: Compositional functionalities influence on ORR with reference to graphite. Fuel 285:119273. https://doi.org/10.1016/j.fuel.2020.119273

    Article  CAS  Google Scholar 

  31. Megaw J, Gilmore BF (2016) Draft genome sequence of Staphylococcus succinus strain CSM-77, a moderately halophilic bacterium isolated from a Triassic salt mine. Genome Announc 4:e00532-e616. https://doi.org/10.1128/genomeA.00532-16

    Article  PubMed  PubMed Central  Google Scholar 

  32. Zhou H, Yao Z, Shi H (2017) Draft genome sequence of Staphylococcus succinus subsp. succinus type strain DSM 14617, isolated from plant and soil inclusions within 25- to 35-million-year-old Dominican amber. Genome Announc 5:e01521-e1616. https://doi.org/10.1128/genomeA.01521-16

    Article  PubMed  PubMed Central  Google Scholar 

  33. Place RB, Hiestand D, Burri S (2002) Staphylococcus succinus subsp. casei subsp. nov., a dominant isolate from a surface ripened cheese. Syst Appl Microbiol 25:353–359. https://doi.org/10.1078/0723-2020-00130

    Article  CAS  PubMed  Google Scholar 

  34. Greppi A, Ferrocino I, La Storia A (2015) Monitoring of the microbiota of fermented sausages by culture independent rRNA-based approaches. Int J Food Microbiol 212:67–75. https://doi.org/10.1016/j.ijfoodmicro.2015.01.016

    Article  CAS  PubMed  Google Scholar 

  35. Gajaraj S, Hu Z (2014) Integration of microbial fuel cell techniques into activated sludge wastewater treatment processes to improve nitrogen removal and reduce sludge production. Chemosphere 117:151–157. https://doi.org/10.1016/j.chemosphere.2014.06.013

    Article  CAS  PubMed  Google Scholar 

  36. Zhang GD, Zhao QL, Jiao Y (2012) Efficient electricity generation from sewage sludge usingbiocathode microbial fuel cell. Water Res 46:43–52. https://doi.org/10.1016/j.watres.2011.10.036

    Article  CAS  PubMed  Google Scholar 

  37. Ling LJ, Yang CY, Li ZB (2021) Electrical performance and application in sewage treatment of an electricigenic strain Stenotrophomonas acidaminiphila EFS1. Microbiology China 48:1504–1513. https://doi.org/10.13344/j.microbiol.china.200820

    Article  CAS  Google Scholar 

  38. Logan BE, Rossi R, Ragab A (2019) Electroactive microorganisms in bioelectrochemical systems. Nat Rev Microbiol 17:307–319. https://doi.org/10.1038/s41579-019-0173-x

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

We are grateful to Northwest Normal University for its cooperation with this study.

Funding

This work was supported in part by Lanzhou Science and Technology Plan Project 2018–1-104; Special funds for guiding the Development of Scientific and technological Innovation in Gansu Province 2019ZX-05; Industrial support Plan Project of Colleges and Universities in Gansu Province 2020C-21.

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All authors contributed to the study conception and design. Material preparation, data collection, and analysis were performed by HL, CY, ZL, and LL. The first draft of the manuscript was written by HL and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

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Correspondence to Lijun Ling.

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Ling, L., Luo, H., Li, Z. et al. Isolation, Identification and Characteristic Analysis of Plant Endophyte Electrogenic Bacteria Shinella zoogloeoides SHE10. Curr Microbiol 79, 268 (2022). https://doi.org/10.1007/s00284-022-02964-9

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