Extracellular electron transfer mechanisms between microorganisms and minerals

Extracellular electron transfer via microbial nanowires

Reguera, G., McCarthy, K. D., Mehta, T., Nicoll, J. S., Tuominen, M. T., & Lovley, D. R. (2005) · Nature · doi:10.1038/nature03661 · Cited by 2,585

Novel Mode of Microbial Energy Metabolism: Organic Carbon Oxidation Coupled to Dissimilatory Reduction of Iron or Manganese

Lovley, D. R., & Phillips, E. J. P. (1988) · Applied and Environmental Microbiology · doi:10.1128/aem.54.6.1472-1480.1988 · Cited by 2,395

Electricity Production by Geobacter sulfurreducens Attached to Electrodes

Bond, D. R., & Lovley, D. R. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.3.1548-1555.2003 · Cited by 2,198

Shewanella secretes flavins that mediate extracellular electron transfer

Marsili, E., Baron, D. B., Shikhare, I. D., Coursolle, D., Gralnick, J. A., & Bond, D. R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710525105 · Cited by 1,982

Humic substances as electron acceptors for microbial respiration

Lovley, D. R., Coates, J. D., Blunt-Harris, E. L., Phillips, E. J. P., & Woodward, J. C. (1996) · Nature · doi:10.1038/382445a0 · Cited by 1,834

Anaerobic Oxidation of Methane: Progress with an Unknown Process

Knittel, K., & Boetius, A. (2009) · Annual Review of Microbiology · doi:10.1146/annurev.micro.61.080706.093130 · Cited by 1,775

Electrically conductive bacterial nanowires produced by Shewanella oneidensis strain MR-1 and other microorganisms

Gorby, Y. A., Yanina, S., McLean, J. S., Rosso, K. M., Moyles, D., Dohnalkova, A., Beveridge, T. J., Chang, I. S., Kim, B. H., Kim, K. S., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604517103 · Cited by 1,749

Microbial electrosynthesis — revisiting the electrical route for microbial production

Rabaey, K., & Rozendal, R. A. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2422 · Cited by 1,651

Semiconducting and Metallic Polymers: The Fourth Generation of Polymeric Materials (Nobel Lecture)

Heeger, A. J. (2001) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20010716)40:14<2591::aid-anie2591>3.0.co;2-0 · Cited by 1,493

Microbial reduction of uranium

Lovley, D. R., Phillips, E. J. P., Gorby, Y. A., & Landa, E. R. (1991) · Nature · doi:10.1038/350413a0 · Cited by 1,446

Electrode-Reducing Microorganisms That Harvest Energy from Marine Sediments

Bond, D. R., Holmes, D. E., Tender, L. M., & Lovley, D. R. (2002) · Science · doi:10.1126/science.1066771 · Cited by 1,437

A new model for electron flow during anaerobic digestion: direct interspecies electron transfer to Methanosaeta for the reduction of carbon dioxide to methane

Rotaru, A.-E., Shrestha, P. M., Liu, F., Shrestha, M., Shrestha, D., Embree, M., Zengler, K., Wardman, C., Nevin, K. P., & Lovley, D. R. (2014) · Energy Environ. Sci. · doi:10.1039/c3ee42189a · Cited by 1,389

Bacterial Manganese Reduction and Growth with Manganese Oxide as the Sole Electron Acceptor

Myers, C. R., & Nealson, K. H. (1988) · Science · doi:10.1126/science.240.4857.1319 · Cited by 1,365

Manganese- and Iron-Dependent Marine Methane Oxidation

Beal, E. J., House, C. H., & Orphan, V. J. (2009) · Science · doi:10.1126/science.1169984 · Cited by 1,075

Direct Exchange of Electrons Within Aggregates of an Evolved Syntrophic Coculture of Anaerobic Bacteria

Summers, Z. M., Fogarty, H. E., Leang, C., Franks, A. E., Malvankar, N. S., & Lovley, D. R. (2010) · Science · doi:10.1126/science.1196526 · Cited by 1,009

Anaerobic production of magnetite by a dissimilatory iron-reducing microorganism

Lovley, D. R., Stolz, J. F., Nord, G. L., & Phillips, E. J. P. (1987) · Nature · doi:10.1038/330252a0 · Cited by 989

Towards environmental systems biology of Shewanella

Fredrickson, J. K., Romine, M. F., Beliaev, A. S., Auchtung, J. M., Driscoll, M. E., Gardner, T. S., Nealson, K. H., Osterman, A. L., Pinchuk, G., Reed, J. L., et al. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1947 · Cited by 971

Metallic transport in polyaniline

Lee, K., Cho, S., Heum Park, S., Heeger, A. J., Lee, C.-W., & Lee, S.-H. (2006) · Nature · doi:10.1038/nature04705 · Cited by 936

Stimulating the In Situ Activity of Geobacter Species To Remove Uranium from the Groundwater of a Uranium-Contaminated Aquifer

Anderson, R. T., Vrionis, H. A., Ortiz-Bernad, I., Resch, C. T., Long, P. E., Dayvault, R., Karp, K., Marutzky, S., Metzler, D. R., Peacock, A., et al. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.10.5884-5891.2003 · Cited by 924

Direct Interspecies Electron Transfer between Geobacter metallireducens and Methanosarcina barkeri

Rotaru, A.-E., Shrestha, P. M., Liu, F., Markovaite, B., Chen, S., Nevin, K. P., & Lovley, D. R. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.00895-14 · Cited by 919

Tunable metallic-like conductivity in microbial nanowire networks

Malvankar, N. S., Vargas, M., Nevin, K. P., Franks, A. E., Leang, C., Kim, B.-C., Inoue, K., Mester, T., Covalla, S. F., Johnson, J. P., et al. (2011) · Nature Nanotechnology · doi:10.1038/nnano.2011.119 · Cited by 912

The interplay of microbially mediated and abiotic reactions in the biogeochemical Fe cycle

Melton, E. D., Swanner, E. D., Behrens, S., Schmidt, C., & Kappler, A. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3347 · Cited by 899

Secretion of Flavins by Shewanella Species and Their Role in Extracellular Electron Transfer

von Canstein, H., Ogawa, J., Shimizu, S., & Lloyd, J. R. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.01387-07 · Cited by 890

Promoting direct interspecies electron transfer with activated carbon

Liu, F., Rotaru, A.-E., Shrestha, P. M., Malvankar, N. S., Nevin, K. P., & Lovley, D. R. (2012) · Energy & Environmental Science · doi:10.1039/c2ee22459c · Cited by 879

Type IV pilus structure and bacterial pathogenicity

Craig, L., Pique, M. E., & Tainer, J. A. (2004) · Nature Reviews Microbiology · doi:10.1038/nrmicro885 · Cited by 766

Promoting Interspecies Electron Transfer with Biochar

Chen, S., Rotaru, A.-E., Shrestha, P. M., Malvankar, N. S., Liu, F., Fan, W., Nevin, K. P., & Lovley, D. R. (2014) · Scientific Reports · doi:10.1038/srep05019 · Cited by 727

Magnetite Particles Triggering a Faster and More Robust Syntrophic Pathway of Methanogenic Propionate Degradation

Cruz Viggi, C., Rossetti, S., Fazi, S., Paiano, P., Majone, M., & Aulenta, F. (2014) · Environmental Science & Technology · doi:10.1021/es5016789 · Cited by 698

Respiration of metal (hydr)oxides by Shewanella and Geobacter: a key role for multihaem c‐type cytochromes

Shi, L., Squier, T. C., Zachara, J. M., & Fredrickson, J. K. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.05783.x · Cited by 664

Shewanella oneidensis MR-1 nanowires are outer membrane and periplasmic extensions of the extracellular electron transport components

Pirbadian, S., Barchinger, S. E., Leung, K. M., Byun, H. S., Jangir, Y., Bouhenni, R. A., Reed, S. B., Romine, M. F., Saffarini, D. A., Shi, L., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1410551111 · Cited by 663

Filamentous bacteria transport electrons over centimetre distances

Pfeffer, C., Larsen, S., Song, J., Dong, M., Besenbacher, F., Meyer, R. L., Kjeldsen, K. U., Schreiber, L., Gorby, Y. A., El-Naggar, M. Y., et al. (2012) · Nature · doi:10.1038/nature11586 · Cited by 661

Single cell activity reveals direct electron transfer in methanotrophic consortia

McGlynn, S. E., Chadwick, G. L., Kempes, C. P., & Orphan, V. J. (2015) · Nature · doi:10.1038/nature15512 · Cited by 654

Microbial interspecies electron transfer via electric currents through conductive minerals

Kato, S., Hashimoto, K., & Watanabe, K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117592109 · Cited by 645

Methanogenesis facilitated by electric syntrophy via (semi)conductive iron‐oxide minerals

Kato, S., Hashimoto, K., & Watanabe, K. (2012) · Environmental Microbiology · doi:10.1111/j.1462-2920.2011.02611.x · Cited by 625

A kinetic perspective on extracellular electron transfer by anode-respiring bacteria

Torres, C. I., Marcus, A. K., Lee, H.-S., Parameswaran, P., Krajmalnik-Brown, R., & Rittmann, B. E. (2010) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2009.00191.x · Cited by 614

Acidithiobacillus ferrooxidans metabolism: from genome sequence to industrial applications

Valdés, J., Pedroso, I., Quatrini, R., Dodson, R. J., Tettelin, H., Blake, R., Eisen, J. A., & Holmes, D. S. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-597 · Cited by 609

Isolation and characterization of novel iron-oxidizing bacteria that grow at circumneutral pH

Emerson, D., & Moyer, C. (1997) · Applied and Environmental Microbiology · doi:10.1128/aem.63.12.4784-4792.1997 · Cited by 578

Current Production and Metal Oxide Reduction by Shewanella oneidensis MR-1 Wild Type and Mutants

Bretschger, O., Obraztsova, A., Sturm, C. A., Chang, I. S., Gorby, Y. A., Reed, S. B., Culley, D. E., Reardon, C. L., Barua, S., Romine, M. F., et al. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.01087-07 · Cited by 574

Electric currents couple spatially separated biogeochemical processes in marine sediment

Nielsen, L. P., Risgaard-Petersen, N., Fossing, H., Christensen, P. B., & Sayama, M. (2010) · Nature · doi:10.1038/nature08790 · Cited by 567

Oxidation of aromatic contaminants coupled to microbial iron reduction

Lovley, D. R., Baedecker, M. J., Lonergan, D. J., Cozzarelli, I. M., Phillips, E. J. P., & Siegel, D. I. (1989) · Nature · doi:10.1038/339297a0 · Cited by 564

Intercellular wiring enables electron transfer between methanotrophic archaea and bacteria

Wegener, G., Krukenberg, V., Riedel, D., Tegetmeyer, H. E., & Boetius, A. (2015) · Nature · doi:10.1038/nature15733 · Cited by 562

The archaeal cell envelope

Albers, S.-V., & Meyer, B. H. (2011) · Nature Reviews Microbiology · doi:10.1038/nrmicro2576 · Cited by 542

Rate enhancement of bacterial extracellular electron transport involves bound flavin semiquinones

Okamoto, A., Hashimoto, K., Nealson, K. H., & Nakamura, R. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1220823110 · Cited by 539

Extracellular electron transfer through microbial reduction of solid-phase humic substances

Roden, E. E., Kappler, A., Bauer, I., Jiang, J., Paul, A., Stoesser, R., Konishi, H., & Xu, H. (2010) · Nature Geoscience · doi:10.1038/ngeo870 · Cited by 509

Characterization of an electron conduit between bacteria and the extracellular environment

Hartshorne, R. S., Reardon, C. L., Ross, D., Nuester, J., Clarke, T. A., Gates, A. J., Mills, P. C., Fredrickson, J. K., Zachara, J. M., Shi, L., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900086106 · Cited by 488

Flavin Electron Shuttles Dominate Extracellular Electron Transfer by Shewanella oneidensis

Kotloski, N. J., & Gralnick, J. A. (2013) · mBio · doi:10.1128/mbio.00553-12 · Cited by 484

The Mtr Respiratory Pathway Is Essential for Reducing Flavins and Electrodes in Shewanella oneidensis

Coursolle, D., Baron, D. B., Bond, D. R., & Gralnick, J. A. (2010) · Journal of Bacteriology · doi:10.1128/jb.00925-09 · Cited by 472

Challenges in microbial fuel cell development and operation

Kim, B. H., Chang, I. S., & Gadd, G. M. (2007) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-007-1027-4 · Cited by 432

Magnetite compensates for the lack of a pilin‐associated c ‐type cytochrome in extracellular electron exchange

Liu, F., Rotaru, A., Shrestha, P. M., Malvankar, N. S., Nevin, K. P., & Lovley, D. R. (2015) · Environmental Microbiology · doi:10.1111/1462-2920.12485 · Cited by 425

Bioenergetic challenges of microbial iron metabolisms

Bird, L. J., Bonnefoy, V., & Newman, D. K. (2011) · Trends in Microbiology · doi:10.1016/j.tim.2011.05.001 · Cited by 423

The first demonstration of a microbial fuel cell as a viable power supply: Powering a meteorological buoy

Tender, L. M., Gray, S. A., Groveman, E., Lowy, D. A., Kauffman, P., Melhado, J., Tyce, R. C., Flynn, D., Petrecca, R., & Dobarro, J. (2008) · Journal of Power Sources · doi:10.1016/j.jpowsour.2007.12.123 · Cited by 390

Carbon cloth stimulates direct interspecies electron transfer in syntrophic co-cultures

Chen, S., Rotaru, A.-E., Liu, F., Philips, J., Woodard, T. L., Nevin, K. P., & Lovley, D. R. (2014) · Bioresource Technology · doi:10.1016/j.biortech.2014.09.009 · Cited by 388

Biochemical and genetic characterization of PpcA, a periplasmic c-type cytochrome in Geobacter sulfurreducens

LLOYD, J. R., LEANG, C., MYERSON, A. L. H., COPPI, M. V., CUIFO, S., METHE, B., SANDLER, S. J., & LOVLEY, D. R. (2003) · Biochemical Journal · doi:10.1042/bj20020597 · Cited by 373

Towards Electrosynthesis in Shewanella: Energetics of Reversing the Mtr Pathway for Reductive Metabolism

Ross, D. E., Flynn, J. M., Baron, D. B., Gralnick, J. A., & Bond, D. R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016649 · Cited by 366

Redox cycling of Fe(II) and Fe(III) in magnetite by Fe-metabolizing bacteria

Byrne, J. M., Klueglein, N., Pearce, C., Rosso, K. M., Appel, E., & Kappler, A. (2015) · Science · doi:10.1126/science.aaa4834 · Cited by 362

Bioreductive deposition of palladium (0) nanoparticles on Shewanella oneidensis with catalytic activity towards reductive dechlorination of polychlorinated biphenyls

Windt, W. D., Aelterman, P., & Verstraete, W. (2005) · Environmental Microbiology · doi:10.1111/j.1462-2920.2005.00696.x · Cited by 362

Electrobiocommodities: powering microbial production of fuels and commodity chemicals from carbon dioxide with electricity

Lovley, D. R., & Nevin, K. P. (2013) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2013.02.012 · Cited by 343

Insight into the evolution of the iron oxidation pathways

Ilbert, M., & Bonnefoy, V. (2013) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2012.10.001 · Cited by 343

Biomineralization of metal-containing ores and concentrates

Rawlings, D. E., Dew, D., & du Plessis, C. (2003) · Trends in Biotechnology · doi:10.1016/s0167-7799(02)00004-5 · Cited by 342

OmcB, a c-Type Polyheme Cytochrome, Involved in Fe(III) Reduction in Geobacter sulfurreducens

Leang, C., Coppi, M. V., & Lovley, D. R. (2003) · Journal of Bacteriology · doi:10.1128/jb.185.7.2096-2103.2003 · Cited by 342

Structure of a bacterial cell surface decaheme electron conduit

Clarke, T. A., Edwards, M. J., Gates, A. J., Hall, A., White, G. F., Bradley, J., Reardon, C. L., Shi, L., Beliaev, A. S., Marshall, M. J., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1017200108 · Cited by 341

Modularity of the Mtr respiratory pathway of Shewanella oneidensis strain MR‐1

Coursolle, D., & Gralnick, J. A. (2010) · Molecular Microbiology · doi:10.1111/j.1365-2958.2010.07266.x · Cited by 315

Hydrogen and Formate Oxidation Coupled to Dissimilatory Reduction of Iron or Manganese by Alteromonas putrefaciens

Lovley, D. R., Phillips, E. J. P., & Lonergan, D. J. (1989) · Applied and Environmental Microbiology · doi:10.1128/aem.55.3.700-706.1989 · Cited by 313

MtrC, an outer membrane decahaem c cytochrome required for metal reduction in Shewanella putrefaciens MR‐1

Beliaev, A. S., Saffarini, D. A., McLaughlin, J. L., & Hunnicutt, D. (2001) · Molecular Microbiology · doi:10.1046/j.1365-2958.2001.02257.x · Cited by 313

Direct and Fe(II)-Mediated Reduction of Technetium by Fe(III)-Reducing Bacteria

Lloyd, J. R., Sole, V. A., Van Praagh, C. V. G., & Lovley, D. R. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.9.3743-3749.2000 · Cited by 283

Shewanella putrefaciens mtrB Encodes an Outer Membrane Protein Required for Fe(III) and Mn(IV) Reduction

Beliaev, A. S., & Saffarini, D. A. (1998) · Journal of Bacteriology · doi:10.1128/.180.23.6292-6297.1998 · Cited by 277

Isolation of a High-Affinity Functional Protein Complex between OmcA and MtrC: Two Outer Membrane Decaheme c -Type Cytochromes of Shewanella oneidensis MR-1

Shi, L., Chen, B., Wang, Z., Elias, D. A., Mayer, M. U., Gorby, Y. A., Ni, S., Lower, B. H., Kennedy, D. W., Wunschel, D. S., et al. (2006) · Journal of Bacteriology · doi:10.1128/jb.01966-05 · Cited by 260

Extracellular reduction of uranium via Geobacter conductive pili as a protective cellular mechanism

Cologgi, D. L., Lampa-Pastirk, S., Speers, A. M., Kelly, S. D., & Reguera, G. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1108616108 · Cited by 244

Electron uptake by iron-oxidizing phototrophic bacteria

Bose, A., Gardel, E. J., Vidoudez, C., Parra, E. A., & Girguis, P. R. (2014) · Nature Communications · doi:10.1038/ncomms4391 · Cited by 236

Comparative genomics of freshwater Fe-oxidizing bacteria: implications for physiology, ecology, and systematics

Emerson, D., Field, E. K., Chertkov, O., Davenport, K. W., Goodwin, L., Munk, C., Nolan, M., & Woyke, T. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00254 · Cited by 235

The ‘porin–cytochrome’ model for microbe‐to‐mineral electron transfer

Richardson, D. J., Butt, J. N., Fredrickson, J. K., Zachara, J. M., Shi, L., Edwards, M. J., White, G., Baiden, N., Gates, A. J., Marritt, S. J., et al. (2012) · Molecular Microbiology · doi:10.1111/j.1365-2958.2012.08088.x · Cited by 231

The pio Operon Is Essential for Phototrophic Fe(II) Oxidation in Rhodopseudomonas palustris TIE-1

Jiao, Y., & Newman, D. K. (2007) · Journal of Bacteriology · doi:10.1128/jb.00776-06 · Cited by 230

Aromatic Amino Acids Required for Pili Conductivity and Long-Range Extracellular Electron Transport in Geobacter sulfurreducens

Vargas, M., Malvankar, N. S., Tremblay, P.-L., Leang, C., Smith, J. A., Patel, P., Synoeyenbos-West, O., Nevin, K. P., & Lovley, D. R. (2013) · mBio · doi:10.1128/mbio.00105-13 · Cited by 230

High-Affinity Binding and Direct Electron Transfer to Solid Metals by the Shewanella oneidensis MR-1 Outer Membrane c-type Cytochrome OmcA

Xiong, Y., Shi, L., Chen, B., Mayer, M. U., Lower, B. H., Londer, Y., Bose, S., Hochella, M. F., Fredrickson, J. K., & Squier, T. C. (2006) · Journal of the American Chemical Society · doi:10.1021/ja063526d · Cited by 221

Rapid electron exchange between surface-exposed bacterial cytochromes and Fe(III) minerals

White, G. F., Shi, Z., Shi, L., Wang, Z., Dohnalkova, A. C., Marshall, M. J., Fredrickson, J. K., Zachara, J. M., Butt, J. N., Richardson, D. J., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1220074110 · Cited by 221

Extracellular respiration of dimethyl sulfoxide by Shewanella oneidensis strain MR-1

Gralnick, J. A., Vali, H., Lies, D. P., & Newman, D. K. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505959103 · Cited by 220

Isolation and Characterization of a Genetically Tractable Photoautotrophic Fe(II)-Oxidizing Bacterium, Rhodopseudomonas palustris Strain TIE-1

Jiao, Y., Kappler, A., Croal, L. R., & Newman, D. K. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.8.4487-4496.2005 · Cited by 219

Electrochemically active biofilms: facts and fiction. A review

Babauta, J., Renslow, R., Lewandowski, Z., & Beyenal, H. (2012) · Biofouling · doi:10.1080/08927014.2012.710324 · Cited by 217

A New Iron-oxidizing/O2-reducing Supercomplex Spanning Both Inner and Outer Membranes, Isolated from the Extreme Acidophile Acidithiobacillus ferrooxidans

Castelle, C., Guiral, M., Malarte, G., Ledgham, F., Leroy, G., Brugna, M., & Giudici-Orticoni, M.-T. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m802496200 · Cited by 215

Visualization of charge propagation along individual pili proteins using ambient electrostatic force microscopy

Malvankar, N. S., Yalcin, S. E., Tuominen, M. T., & Lovley, D. R. (2014) · Nature Nanotechnology · doi:10.1038/nnano.2014.236 · Cited by 210

A trans‐outer membrane porin‐cytochrome protein complex for extracellular electron transfer by G eobacter sulfurreducens PCA

Liu, Y., Wang, Z., Liu, J., Levar, C., Edwards, M. J., Babauta, J. T., Kennedy, D. W., Shi, Z., Beyenal, H., Bond, D. R., et al. (2014) · Environmental Microbiology Reports · doi:10.1111/1758-2229.12204 · Cited by 208

Sulfur, iron-, and calcium cycling associated with natural electric currents running through marine sediment

Risgaard-Petersen, N., Revil, A., Meister, P., & Nielsen, L. P. (2012) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2012.05.036 · Cited by 204

Role of the Tetraheme Cytochrome CymA in Anaerobic Electron Transport in Cells of Shewanella putrefaciens MR-1 with Normal Levels of Menaquinone

Myers, J. M., & Myers, C. R. (2000) · Journal of Bacteriology · doi:10.1128/jb.182.1.67-75.2000 · Cited by 203

Identification and Characterization of MtoA: A Decaheme c-Type Cytochrome of the Neutrophilic Fe(II)-Oxidizing Bacterium Sideroxydans lithotrophicus ES-1

Liu, J., Wang, Z., Belchik, S. M., Edwards, M. J., Liu, C., Kennedy, D. W., Merkley, E. D., Lipton, M. S., Butt, J. N., Richardson, D. J., et al. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00037 · Cited by 202

Transcriptomic and Genetic Analysis of Direct Interspecies Electron Transfer

Shrestha, P. M., Rotaru, A.-E., Summers, Z. M., Shrestha, M., Liu, F., & Lovley, D. R. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.03837-12 · Cited by 195

Surface multiheme c -type cytochromes from Thermincola potens and implications for respiratory metal reduction by Gram-positive bacteria

Carlson, H. K., Iavarone, A. T., Gorur, A., Yeo, B. S., Tran, R., Melnyk, R. A., Mathies, R. A., Auer, M., & Coates, J. D. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112905109 · Cited by 195

Conductivity of individual Geobacter pili

Adhikari, R. Y., Malvankar, N. S., Tuominen, M. T., & Lovley, D. R. (2016) · RSC Advances · doi:10.1039/c5ra28092c · Cited by 194

Structural Basis for Metallic-Like Conductivity in Microbial Nanowires

Malvankar, N. S., Vargas, M., Nevin, K., Tremblay, P.-L., Evans-Lutterodt, K., Nykypanchuk, D., Martz, E., Tuominen, M. T., & Lovley, D. R. (2015) · mBio · doi:10.1128/mbio.00084-15 · Cited by 192

Reduction of low potential electron acceptors requires the CbcL inner membrane cytochrome of Geobacter sulfurreducens

Zacharoff, L. A., Chan, C. H., & Bond, D. R. (2015) · Bioelectrochemistry · doi:10.1016/j.bioelechem.2015.08.003 · Cited by 188

Cable bacteria generate a firewall against euxinia in seasonally hypoxic basins

Seitaj, D., Schauer, R., Sulu-Gambari, F., Hidalgo-Martinez, S., Malkin, S. Y., Burdorf, L. D. W., Slomp, C. P., & Meysman, F. J. R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510152112 · Cited by 183

Natural occurrence of microbial sulphur oxidation by long-range electron transport in the seafloor

Malkin, S. Y., Rao, A. M. F., Seitaj, D., Vasquez-Cardenas, D., Zetsche, E.-M., Hidalgo-Martinez, S., Boschker, H. T. S., & Meysman, F. J. R. (2014) · The ISME Journal · doi:10.1038/ismej.2014.41 · Cited by 181

An Inner Membrane Cytochrome Required Only for Reduction of High Redox Potential Extracellular Electron Acceptors

Levar, C. E., Chan, C. H., Mehta-Kolte, M. G., & Bond, D. R. (2014) · mBio · doi:10.1128/mbio.02034-14 · Cited by 171

Mtr extracellular electron-transfer pathways in Fe(III)-reducing or Fe(II)-oxidizing bacteria: a genomic perspective

Shi, L., Rosso, K. M., Zachara, J. M., & Fredrickson, J. K. (2012) · Biochemical Society Transactions · doi:10.1042/bst20120098 · Cited by 167

Characterization of Protein-Protein Interactions Involved in Iron Reduction by Shewanella oneidensis MR-1

Ross, D. E., Ruebush, S. S., Brantley, S. L., Hartshorne, R. S., Clarke, T. A., Richardson, D. J., & Tien, M. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00146-07 · Cited by 160

Cable Bacteria in Freshwater Sediments

Risgaard‐Petersen, N., Kristiansen, M., Frederiksen, R. B., Dittmer, A. L., Bjerg, J. T., Trojan, D., Schreiber, L., Damgaard, L. R., Schramm, A., & Nielsen, L. P. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.01064-15 · Cited by 159

Redox Linked Flavin Sites in Extracellular Decaheme Proteins Involved in Microbe-Mineral Electron Transfer.

Edwards, M. J., White, G. F., Norman, M., Tome-Fernandez, A., Ainsworth, E., Shi, L., Fredrickson, J. K., Zachara, J. M., Butt, J. N., Richardson, D. J., et al. (2015) · Scientific Reports · doi:10.1038/srep11677 · Cited by 159

Mariprofundus ferrooxydans PV-1 the First Genome of a Marine Fe(II) Oxidizing Zetaproteobacterium

Singer, E., Emerson, D., Webb, E. A., Barco, R. A., Kuenen, J. G., Nelson, W. C., Chan, C. S., Comolli, L. R., Ferriera, S., Johnson, J. H., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025386 · Cited by 157

Cable Bacteria Control Iron–Phosphorus Dynamics in Sediments of a Coastal Hypoxic Basin

Sulu‐Gambari, F., Seitaj, D., Meysman, F. J. R., Schauer, R., Polerecký, L., & Slomp, C. P. (2015) · Environmental Science & Technology · doi:10.1021/acs.est.5b04369 · Cited by 153

Structure and mechanism of the flavocytochrome c fumarate reductase of Shewanella putrefaciens MR-1.

BEEUMEN, J. V., Leys, D., Tsapin, A. S., Nealson, K. H., Meyer, T. E., & Cusanovich, M. A. (1999) · Nature Structural Biology · doi:10.1038/70051 · Cited by 151

Multistep hopping and extracellular charge transfer in microbial redox chains

Pirbadian, S., & El‐Naggar, M. Y. (2012) · Physical Chemistry Chemical Physics · doi:10.1039/c2cp41185g · Cited by 150

A dynamic periplasmic electron transfer network enables respiratory flexibility beyond a thermodynamic regulatory regime

Sturm, G., Richter, K., Dötsch, A., Heide, H., Louro, R. O., & Gescher, J. (2015) · The ISME Journal · doi:10.1038/ismej.2014.264 · Cited by 145

Electrochemical interaction of Shewanella oneidensis MR-1 and its outer membrane cytochromes OmcA and MtrC with hematite electrodes

Meitl, L. A., Eggleston, C. M., Colberg, P. J. S., Khare, N., Reardon, C. L., & Shi, L. (2009) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2009.06.021 · Cited by 140

A functional description of CymA, an electron-transfer hub supporting anaerobic respiratory flexibility in Shewanella

Marritt, S. J., Lowe, T. G., Bye, J. W., McMillan, D. G. G., Shi, L., Fredrickson, J. K., Zachara, J. M., Richardson, D. J., Cheesman, M. R., Jeuken, L. J. C., et al. (2012) · Biochemical Journal · doi:10.1042/bj20120197 · Cited by 139

Specific Bonds between an Iron Oxide Surface and Outer Membrane Cytochromes MtrC and OmcA from Shewanella oneidensis MR-1

Lower, B. H., Shi, L., Yongsunthon, R., Droubay, T. C., McCready, D. E., & Lower, S. K. (2007) · Journal of Bacteriology · doi:10.1128/jb.01518-06 · Cited by 138

Direct Involvement of Type II Secretion System in Extracellular Translocation of Shewanella oneidensis Outer Membrane Cytochromes MtrC and OmcA

Shi, L., Deng, S. H., Marshall, M. J., Wang, Z.-M., Kennedy, D. W., Dohnalkova, A. C., Mottaz, H. M., Hill, E. A., Gorby, Y. A., Beliaev, A. S., et al. (2008) · Journal of Bacteriology · doi:10.1128/jb.00514-08 · Cited by 135

Biological Redox Cycling of Iron in Nontronite and Its Potential Application in Nitrate Removal

Zhao, L., Dong, H., Kukkadapu, R., Zeng, Q., Edelmann, R. E., Pentrak, M. P., & Agrawal, A. (2015) · Environmental Science & Technology · doi:10.1021/acs.est.5b00131 · Cited by 133

Anaerobic Benzene Oxidation via Phenol in Geobacter metallireducens

Zhang, T., Tremblay, P., Chaurasia, A. K., Smith, J. A., Bain, T. S., & Lovley, D. R. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.03134-13 · Cited by 132

The geochemical fingerprint of microbial long-distance electron transport in the seafloor

Meysman, F. J. R., Risgaard‐Petersen, N., Malkin, S. Y., & Nielsen, L. P. (2014) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2014.12.014 · Cited by 130

MtrB Is Required for Proper Incorporation of the Cytochromes OmcA and OmcB into the Outer Membrane of Shewanella putrefaciens MR-1

Myers, C. R., & Myers, J. M. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.11.5585-5594.2002 · Cited by 126

Thermodynamic Characterization of a Triheme Cytochrome Family from Geobacter sulfurreducens Reveals Mechanistic and Functional Diversity

Morgado, L., Bruix, M., Pessanha, M., Londer, Y. Y., & Salgueiro, C. A. (2010) · Biophysical Journal · doi:10.1016/j.bpj.2010.04.017 · Cited by 125

Investigating different mechanisms for biogenic selenite transformations:Geobacter sulfurreducens,Shewanella oneidensisandVeillonella atypica

Pearce, C. I., Pattrick, R. A. D., Law, N., Charnock, J., Coker, V. S., Fellowes, J. W., Oremland, R. S., & Lloyd, J. R. (2009) · Environmental Technology · doi:10.1080/09593330902984751 · Cited by 123

Structure of the Type IVa Major Pilin from the Electrically Conductive Bacterial Nanowires of Geobacter sulfurreducens

Reardon, P. N., & Mueller, K. T. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.498527 · Cited by 123

Redox Reactions of Reduced Flavin Mononucleotide (FMN), Riboflavin (RBF), and Anthraquinone-2,6-disulfonate (AQDS) with Ferrihydrite and Lepidocrocite

Shi, Z., Zachara, J. M., Shi, L., Wang, Z.-M., Moore, D. A., Kennedy, D. W., & Fredrickson, J. K. (2012) · Environmental Science & Technology · doi:10.1021/es301544b · Cited by 122

Thermally activated charge transport in microbial protein nanowires

Lampa-Pastirk, S., Veazey, J. P., Walsh, K. A., Feliciano, G. T., Steidl, R. J., Tessmer, S., & Reguera, G. (2016) · Scientific Reports · doi:10.1038/srep23517 · Cited by 121

Microbial Lithotrophic Oxidation of Structural Fe(II) in Biotite

Shelobolina, E. S., Xu, H., Konishi, H., Kukkadapu, R., Wu, T., Blöthe, M., & Roden, E. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.01034-12 · Cited by 118

Crystal Structures at Atomic Resolution Reveal the Novel Concept of “Electron-harvesting” as a Role for the Small Tetraheme Cytochrome c

Leys, D., Meyer, T. E., Tsapin, A. S., Nealson, K. H., Cusanovich, M. A., & BEEUMEN, J. V. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m203866200 · Cited by 115

Menaquinone-7 Is Specific Cofactor in Tetraheme Quinol Dehydrogenase CymA

McMillan, D. G. G., Marritt, S. J., Butt, J. N., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.348813 · Cited by 110

Antibody Recognition Force Microscopy Shows that Outer Membrane Cytochromes OmcA and MtrC Are Expressed on the Exterior Surface of Shewanella oneidensis MR-1

Lower, B. H., Yongsunthon, R., Shi, L., Wildling, L., Gruber, H. J., Wigginton, N. S., Reardon, C. L., Pinchuk, G. E., Droubay, T. C., Boily, J., et al. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.02108-08 · Cited by 109

Anaerobic Benzene Oxidation by Geobacter Species

Zhang, T., Bain, T. S., Nevin, K. P., Barlett, M. A., & Lovley, D. R. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.02469-12 · Cited by 107

Optimizing Cr(VI) and Tc(VII) Remediation through Nanoscale Biomineral Engineering

Cutting, R. S., Coker, V. S., Telling, N. D., Kimber, R. L., Pearce, C. I., Ellis, B. L., Lawson, R. S., van der Laan, G., Pattrick, R. A. D., Vaughan, D. J., et al. (2010) · Environmental Science & Technology · doi:10.1021/es902119u · Cited by 106

Evidence that OmcB and OmpB ofGeobacter sulfurreducensare outer membrane surface proteins

Qian, X., Reguera, G., Mester, T., & Lovley, D. R. (2007) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2007.00915.x · Cited by 105

Microbially Driven Fenton Reaction for Degradation of the Widespread Environmental Contaminant 1,4-Dioxane

Sekar, R., & DiChristina, T. J. (2014) · Environmental Science & Technology · doi:10.1021/es503454a · Cited by 104

Structural and functional insights into the conductive pili of Geobacter sulfurreducens revealed in molecular dynamics simulations

Feliciano, G. T., Steidl, R. J., & Reguera, G. (2015) · Physical Chemistry Chemical Physics · doi:10.1039/c5cp03432a · Cited by 103

Effects of temperature and dissolved oxygen on Se(IV) removal and Se(0) precipitation by Shewanella sp. HN-41

Lee, J.-H., Han, J., Choi, H., & Hur, H. (2007) · Chemosphere · doi:10.1016/j.chemosphere.2007.02.062 · Cited by 102

Genomic analyses of bacterial porin-cytochrome gene clusters

Shi, L., Fredrickson, J. K., & Zachara, J. M. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00657 · Cited by 101

A Previously Uncharacterized, Nonphotosynthetic Member of the Chromatiaceae Is the Primary CO 2 -Fixing Constituent in a Self-Regenerating Biocathode

Wang, Z., Leary, D. H., Malanoski, A. P., Li, R. W., Hervey, W. J., Eddie, B., Tender, G. S., Yanosky, S. G., Vora, G. J., Tender, L. M., et al. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.02947-14 · Cited by 88

Modeling biofilms with dual extracellular electron transfer mechanisms

Renslow, R. S., Babauta, J. T., Kuprat, A. P., Schenk, J., Ivory, C. F., Fredrickson, J. K., & Beyenal, H. (2013) · Physical Chemistry Chemical Physics · doi:10.1039/c3cp53759e · Cited by 83

Direct involvement of ombB, omaB, and omcB genes in extracellular reduction of Fe(III) by Geobacter sulfurreducens PCA

Liu, Y., Fredrickson, J. K., Zachara, J. M., & Shi, L. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01075 · Cited by 81

Formation of single domain magnetite by green rust oxidation promoted by microbial anaerobic nitrate-dependent iron oxidation

Miot, J., Li, J., Benzerara, K., Sougrati, M. T., Ona-Nguéma, G., Bernard, S., Jumas, J. C., & Guyot, F. (2014) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2014.04.047 · Cited by 80

Controlled cobalt doping in biogenic magnetite nanoparticles

Byrne, J. M., Coker, V. S., Moise, S., Wincott, P. L., Vaughan, D. J., Tuna, F., Arenholz, E., van der Laan, G., Pattrick, R. A. D., Lloyd, J. R., et al. (2013) · Journal of The Royal Society Interface · doi:10.1098/rsif.2013.0134 · Cited by 77

Protein–Protein Interaction Regulates the Direction of Catalysis and Electron Transfer in a Redox Enzyme Complex

McMillan, D. G., Marritt, S., Firer-Sherwood, M. A., Shi, L., Richardson, D., Evans, S., Elliott, S., Butt, J., & Jeuken, L. (2013) · Journal of the American Chemical Society · doi:10.1021/ja405072z · Cited by 76

Redox Interactions Between Cr(VI) and Fe(II) in Bioreduced Biotite and Chlorite

Brookshaw, D. R., Coker, V. S., Lloyd, J. R., Vaughan, D. J., & Pattrick, R. A. D. (2014) · Environmental Science & Technology · doi:10.1021/es5031849 · Cited by 73

In Vivo Identification of the Outer Membrane Protein OmcA−MtrC Interaction Network in Shewanella oneidensis MR-1 Cells Using Novel Hydrophobic Chemical Cross-Linkers

Zhang, H., Tang, X., Munske, G. R., Zakharova, N., Yang, L., Zheng, C., Wolff, M. A., Tolić, N., Anderson, G., Shi, L., et al. (2008) · Journal of Proteome Research · doi:10.1021/pr7007658 · Cited by 72

Molecular and Electronic Structure of the Peptide Subunit of Geobacter sulfurreducens Conductive Pili from First Principles

Feliciano, G. T., da Silva, A. J. R., Reguera, G., & Artacho, E. (2012) · The Journal of Physical Chemistry A · doi:10.1021/jp302232p · Cited by 66

Characterization of MtoD from Sideroxydans lithotrophicus: a cytochrome c electron shuttle used in lithoautotrophic growth

Beckwith, C., Edwards, M. J., Lawes, M. C., Shi, L., Butt, J. N., Richardson, D. J., & Clarke, T. A. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.00332 · Cited by 65

Characterization of the Decaheme c-Type Cytochrome OmcA in Solution and on Hematite Surfaces by Small Angle X-Ray Scattering and Neutron Reflectometry

Johs, A., Shi, L., Droubay, T. C., Ankner, J. F., & Liang, L. (2010) · Biophysical Journal · doi:10.1016/j.bpj.2010.03.049 · Cited by 63

Effects of soluble flavin on heterogeneous electron transfer between surface-exposed bacterial cytochromes and iron oxides

Wang, Z.-M., Shi, Z., Shi, L., White, G. F., Richardson, D. J., Clarke, T. A., Fredrickson, J. K., & Zachara, J. M. (2015) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2015.03.039 · Cited by 52

Potential Function of Added Minerals as Nucleation Sites and Effect of Humic Substances on Mineral Formation by the Nitrate-Reducing Fe(II)-Oxidizer Acidovorax sp. BoFeN1

Dippon, U., Pantke, C., Porsch, K., Larese-Casanova, P., & Kappler, A. A. (2012) · Environmental Science & Technology · doi:10.1021/es2046266 · Cited by 51

Reductive dissolution of goethite and hematite by reduced flavins

Shi, Z., Zachara, J. M., Wang, Z.-M., Shi, L., & Fredrickson, J. K. (2013) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2013.05.039 · Cited by 49

Tools for resolving complexity in the electron transfer networks of multiheme cytochromes c

Firer-Sherwood, M. A., Bewley, K. D., Mock, J., & Elliott, S. J. (2011) · Metallomics · doi:10.1039/c0mt00097c · Cited by 44

Inter‐Aromatic Distances in Geobacter Sulfurreducens Pili Relevant to Biofilm Charge Transport

Yan, H., Chuang, C., Zhugayevych, A., Tretiak, S., Dahlquist, F. W., & Bazan, G. C. (2015) · Advanced Materials · doi:10.1002/adma.201404167 · Cited by 43

Engineering Biogenic Magnetite for Sustained Cr(VI) Remediation in Flow-through Systems

Crean, D. E., Coker, V. S., van der Laan, G., & Lloyd, J. R. (2012) · Environmental Science & Technology · doi:10.1021/es2037146 · Cited by 41

Biooxidation of a gold concentrate in a continuous stirred tank reactor: mathematical model and optimal configuration

González, R., Gentina, J. C., & Acevedo, F. (2003) · Biochemical Engineering Journal · doi:10.1016/j.bej.2003.09.007 · Cited by 37

Identification of genes specifically required for the anaerobic metabolism of benzene in Geobacter metallireducens

Zhang, T., Tremblay, P., Chaurasia, A. K., Smith, J. A., Bain, T. S., & Lovley, D. R. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00245 · Cited by 34

Bioremediation via Microbial Metal Reduction

Watts, M. P., & Lloyd, J. R. (2012) · Springer eBooks · doi:10.1007/978-3-642-32867-1_7 · Cited by 20

Dynamic interactions at the mineral–organic matter interface

Kleber, M., Bourg, I. C., Coward, E. K., Hansel, C. M., Myneni, S. C. B., & Nunan, N. (2021) · Nature Reviews Earth & Environment · doi:10.1038/s43017-021-00162-y · Cited by 1,254

A flavin-based extracellular electron transfer mechanism in diverse Gram-positive bacteria

Light, S. H., Su, L., Rivera-Lugo, R., Cornejo, J. A., Louie, A., Iavarone, A. T., Ajo-Franklin, C. M., & Portnoy, D. A. (2018) · Nature · doi:10.1038/s41586-018-0498-z · Cited by 632

A critical review of mineral-microbe interaction and co-evolution: Mechanisms and applications

Dong, H., Huang, L., Zhao, L., Zeng, Q., Liu, X., Sheng, Y., Shi, L., Wu, G., Jiang, H., Li, F., et al. (2022) · National Science Review · doi:10.1093/nsr/nwac128 · Cited by 472

Insight into interactions between syntrophic bacteria and archaea in anaerobic digestion amended with conductive materials

Kumar, V., Nabaterega, R., Khoei, S., & Eskicioglu, C. (2021) · Renewable and Sustainable Energy Reviews · doi:10.1016/j.rser.2021.110965 · Cited by 93

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Wang, D., Tan, J., Zhu, H., Mei, Y., & Liu, X. (2021) · Advanced Science · doi:10.1002/advs.202004393 · Cited by 49