Possibilities for Extremophilic Microorganisms in Microbial Electrochemical Systems

Overview

Journal FEMS Microbiol Rev

Publisher Oxford University Press

Specialty Microbiology

Date 2015 Oct 18

PMID 26474966

Citations 22

Authors

Mark Dopson

Gaofeng Ni

Tom H J A Sleutels

Affiliations

Soon will be listed here.

Abstract

Microbial electrochemical systems exploit the metabolism of microorganisms to generate electrical energy or a useful product. In the past couple of decades, the application of microbial electrochemical systems has increased from the use of wastewaters to produce electricity to a versatile technology that can use numerous sources for the extraction of electrons on the one hand, while on the other hand these electrons can be used to serve an ever increasing number of functions. Extremophilic microorganisms grow in environments that are hostile to most forms of life and their utilization in microbial electrochemical systems has opened new possibilities to oxidize substrates in the anode and produce novel products in the cathode. For example, extremophiles can be used to oxidize sulfur compounds in acidic pH to remediate wastewaters, generate electrical energy from marine sediment microbial fuel cells at low temperatures, desalinate wastewaters and act as biosensors of low amounts of organic carbon. In this review, we will discuss the recent advances that have been made in using microbial catalysts under extreme conditions and show possible new routes that extremophilic microorganisms open for microbial electrochemical systems.

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References

Lovley D, Malvankar N . Seeing is believing: novel imaging techniques help clarify microbial nanowire structure and function. Environ Microbiol. 2014; 17(7):2209-15. DOI: 10.1111/1462-2920.12708. View

Rozendal R, Hamelers H, Buisman C . Effects of membrane cation transport on pH and microbial fuel cell performance. Environ Sci Technol. 2006; 40(17):5206-11. DOI: 10.1021/es060387r. View

Mathis B, Marshall C, Milliken C, Makkar R, Creager S, May H . Electricity generation by thermophilic microorganisms from marine sediment. Appl Microbiol Biotechnol. 2007; 78(1):147-55. DOI: 10.1007/s00253-007-1266-4. View

Cheng S, Xing D, Logan B . Electricity generation of single-chamber microbial fuel cells at low temperatures. Biosens Bioelectron. 2010; 26(5):1913-7. DOI: 10.1016/j.bios.2010.05.016. View

Ma C, Zhuang L, Zhou S, Yang G, Yuan Y, Xu R . Alkaline extracellular reduction: isolation and characterization of an alkaliphilic and halotolerant bacterium, Bacillus pseudofirmus MC02. J Appl Microbiol. 2012; 112(5):883-91. DOI: 10.1111/j.1365-2672.2012.05276.x. View

Ter Heijne A, Hamelers H, Buisman C . Microbial fuel cell operation with continuous biological ferrous iron oxidation of the catholyte. Environ Sci Technol. 2007; 41(11):4130-4. DOI: 10.1021/es0702824. View

San Martin-Uriz P, Gomez M, Arcas A, Bargiela R, Amils R . Draft genome sequence of the electricigen Acidiphilium sp. strain PM (DSM 24941). J Bacteriol. 2011; 193(19):5585-6. PMC: 3187463. DOI: 10.1128/JB.05386-11. View

Strik D, Timmers R, Helder M, Steinbusch K, Hamelers H, Buisman C . Microbial solar cells: applying photosynthetic and electrochemically active organisms. Trends Biotechnol. 2010; 29(1):41-9. DOI: 10.1016/j.tibtech.2010.10.001. View

Lefebvre O, Tan Z, Kharkwal S, Ng H . Effect of increasing anodic NaCl concentration on microbial fuel cell performance. Bioresour Technol. 2012; 112:336-40. DOI: 10.1016/j.biortech.2012.02.048. View

10.

Bonnefoy V, Holmes D . Genomic insights into microbial iron oxidation and iron uptake strategies in extremely acidic environments. Environ Microbiol. 2011; 14(7):1597-611. DOI: 10.1111/j.1462-2920.2011.02626.x. View

11.

Yoon J, Yeo S, Kim I, Oh T . Shewanella marisflavi sp. nov. and Shewanella aquimarina sp. nov., slightly halophilic organisms isolated from sea water of the Yellow Sea in Korea. Int J Syst Evol Microbiol. 2004; 54(Pt 6):2347-2352. DOI: 10.1099/ijs.0.63198-0. View

12.

Kim J, Dec J, Bruns M, Logan B . Removal of odors from Swine wastewater by using microbial fuel cells. Appl Environ Microbiol. 2008; 74(8):2540-3. PMC: 2293147. DOI: 10.1128/AEM.02268-07. View

13.

Hoehler T, Jorgensen B . Microbial life under extreme energy limitation. Nat Rev Microbiol. 2013; 11(2):83-94. DOI: 10.1038/nrmicro2939. View

14.

Rozendal R, Hamelers H, Rabaey K, Keller J, Buisman C . Towards practical implementation of bioelectrochemical wastewater treatment. Trends Biotechnol. 2008; 26(8):450-9. DOI: 10.1016/j.tibtech.2008.04.008. View

15.

Hamelers H, Ter Heijne A, Stein N, Rozendal R, Buisman C . Butler-Volmer-Monod model for describing bio-anode polarization curves. Bioresour Technol. 2010; 102(1):381-7. DOI: 10.1016/j.biortech.2010.06.156. View

16.

Badalamenti J, Krajmalnik-Brown R, Torres C . Generation of high current densities by pure cultures of anode-respiring Geoalkalibacter spp. under alkaline and saline conditions in microbial electrochemical cells. mBio. 2013; 4(3):e00144-13. PMC: 3648901. DOI: 10.1128/mBio.00144-13. View

17.

Parameswaran P, Bry T, Popat S, Lusk B, Rittmann B, Torres C . Kinetic, electrochemical, and microscopic characterization of the thermophilic, anode-respiring bacterium Thermincola ferriacetica. Environ Sci Technol. 2013; 47(9):4934-40. DOI: 10.1021/es400321c. View

18.

Kuntke P, Smiech K, Bruning H, Zeeman G, Saakes M, Sleutels T . Ammonium recovery and energy production from urine by a microbial fuel cell. Water Res. 2012; 46(8):2627-36. DOI: 10.1016/j.watres.2012.02.025. View

19.

Rabaey K, Rozendal R . Microbial electrosynthesis - revisiting the electrical route for microbial production. Nat Rev Microbiol. 2010; 8(10):706-16. DOI: 10.1038/nrmicro2422. View

20.

Paul V, Minteer S, Treu B, R Mormile M . Ability of a haloalkaliphilic bacterium isolated from Soap Lake, Washington to generate electricity at pH 11.0 and 7% salinity. Environ Technol. 2014; 35(5-8):1003-11. DOI: 10.1080/09593330.2013.858186. View