The Periplasmic Nitrate Reductase Nap Is Required for Anaerobic Growth and Involved in Redox Control of Magnetite Biomineralization in Magnetospirillum gryphiswaldense

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302

Cell biology and molecular basis of denitrification

Zumft, W. G. (1997) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.61.4.533-616.1997 · Cited by 3,560

Vesiclepedia: A Compendium for Extracellular Vesicles with Continuous Community Annotation

Kalra, H., Simpson, R. J., Ji, H., Aikawa, E., Altevogt, P., Askenase, P., Bond, V. C., Borràs, F. E., Breakefield, X., Budnik, V., et al. (2012) · PLoS Biology · doi:10.1371/journal.pbio.1001450 · Cited by 1,367

Magnetosomes Are Cell Membrane Invaginations Organized by the Actin-Like Protein MamK

Komeili, A., Li, Z., Newman, D. K., & Jensen, G. J. (2005) · Science · doi:10.1126/science.1123231 · Cited by 647

An acidic protein aligns magnetosomes along a filamentous structure in magnetotactic bacteria

Scheffel, A., Gruska, M., Faivre, D., Linaroudis, A. A., Plitzko, J. M., & Schüler, D. (2005) · Nature · doi:10.1038/nature04382 · Cited by 537

Microbial nitrate respiration – Genes, enzymes and environmental distribution

Kraft, B., Strous, M., & Tegetmeyer, H. E. (2011) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2010.12.025 · Cited by 485

Functional, biochemical and genetic diversity of prokaryotic nitrate reductases

Richardson, D. J., Berks, B. C., Russell, D. A., Spiro, S., & Taylor, C. J. (2001) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000845 · Cited by 477

Magneto-aerotaxis in marine coccoid bacteria

Frankel, R. B., Bazylinski, D. A., Johnson, M. S., & Taylor, B. L. (1997) · Biophysical Journal · doi:10.1016/s0006-3495(97)78132-3 · Cited by 466

Expression of denitrification enzymes in response to the dissolved oxygen level and respiratory substrate in continuous culture of Pseudomonas stutzeri

Körner, H., & Zumft, W. G. (1989) · Applied and Environmental Microbiology · doi:10.1128/aem.55.7.1670-1676.1989 · Cited by 406

Growth and magnetosome formation by microaerophilic Magnetospirillum strains in an oxygen-controlled fermentor

Heyen, U., & Schüler, D. (2003) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-002-1219-x · Cited by 381

Magnetosome biogenesis in magnetotactic bacteria

Uebe, R., & Schüler, D. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.99 · Cited by 552

Ecology, Diversity, and Evolution of Magnetotactic Bacteria

Lefèvre, C., & Bazylinski, D. (2013) · Microbiology and Molecular Reviews · doi:10.1128/mmbr.00021-13 · Cited by 391

Nitrate and periplasmic nitrate reductases

Sparacino-Watkins, C., Stolz, J. F., & Basu, P. (2014) · Chem. Soc. Rev. · doi:10.1039/c3cs60249d · Cited by 426

The prokaryotic Mo/W-bisPGD enzymes family: A catalytic workhorse in bioenergetic

Grimaldi, S., Schoepp‐Cothenet, B., Ceccaldi, P., Guigliarelli, B., & Magalon, A. (2013) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2013.01.011 · Cited by 164

A newly discovered function of nitrate reductase in chemoautotrophic vanadate transformation by natural mackinawite in aquifer

He, C., Zhang, B., Lü, J., & Qiu, R. (2020) · Water Research · doi:10.1016/j.watres.2020.116664 · Cited by 148

Comparative genomic analysis of magnetotactic bacteria from the Deltaproteobacteria provides new insights into magnetite and greigite magnetosome genes required for magnetotaxis.

Lefèvre, C., Trubitsyn, D., Abreu, F., Kolinko, S., Jogler, C., de Almeida, L. D., de Vasconcelos, A. D., Kube, M., Reinhardt, R., Lins, U., et al. (2013) · Environmental Microbiology · doi:10.1111/1462-2920.12128 · Cited by 113

Polarity of bacterial magnetotaxis is controlled by aerotaxis through a common sensory pathway

Popp, F., Armitage, J. P., & Schüler, D. (2014) · Nature Communications · doi:10.1038/ncomms6398 · Cited by 98

The magnetosome proteins MamX , MamZ and MamH are involved in redox control of magnetite biomineralization in M agnetospirillum gryphiswaldense

Raschdorf, O., Müller, F. D., Pósfai, M., Plitzko, J. M., & Schüler, D. (2013) · Molecular Microbiology · doi:10.1111/mmi.12317 · Cited by 94

Magnetic genes: Studying the genetics of biomineralization in magnetotactic bacteria

McCausland, H. C., & Komeili, A. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008499 · Cited by 93

The Bacterial Magnetosome: A Unique Prokaryotic Organelle

Lower, B. H., & Bazylinski, D. A. (2013) · Microbial Physiology · doi:10.1159/000346543 · Cited by 87

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 74

Aerobic and anaerobic removal of lead and mercury via calcium carbonate precipitation mediated by statistically optimized nitrate reductases

Eltarahony, M. M., Zaki, S. A. E. F., & Abd-El-Haleem, D. A. M. (2020) · Scientific Reports · doi:10.1038/s41598-020-60951-1 · Cited by 69

Enzyme-Specific Coupling of Oxygen and Nitrogen Isotope Fractionation of the Nap and Nar Nitrate Reductases

Asamoto, C. K., Rempfert, K. R., Luu, V. H., Younkin, A. D., & Kopf, S. (2021) · Environmental Science & Technology · doi:10.1021/acs.est.0c07816 · Cited by 72

Chemical signature of magnetotactic bacteria

Amor, M., Busigny, V., Durand‐Dubief, M., Tharaud, M., Ona-Nguéma, G., Gélabert, A., Alphandéry, E., Menguy, N., Benedetti, M. F., Chebbi, I., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414112112 · Cited by 69

Genetic and biochemical investigations of the role of MamP in redox control of iron biomineralization in Magnetospirillum magneticum

Jones, S. R., Wilson, T. D., Brown, M. E., Rahn-Lee, L., Yu, Y., Fredriksen, L. L., Ozyamak, E., Komeili, A., & Chang, M. C. Y. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1417614112 · Cited by 66

A Genetic Strategy for Probing the Functional Diversity of Magnetosome Formation

Rahn-Lee, L., Byrne, M. E., Zhang, M., Sage, D. L., Glenn, D. R., Milbourne, T., Walsworth, R. L., Vali, H., & Komeili, A. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1004811 · Cited by 64

Cytochrome cd1 Nitrite Reductase NirS Is Involved in Anaerobic Magnetite Biomineralization in Magnetospirillum gryphiswaldense and Requires NirN for Proper d1 Heme Assembly

Li, Y., Bali, S., Borg, S., Katzmann, E., Ferguson, S. J., & Schüler, D. (2013) · Journal of Bacteriology · doi:10.1128/jb.00686-13 · Cited by 61

Overproduction of Magnetosomes by Genomic Amplification of Biosynthesis-Related Gene Clusters in a Magnetotactic Bacterium

Lohße, A., Kolinko, I., Raschdorf, O., Uebe, R., Borg, S., Brachmann, A., Plitzko, J. M., Müller, R., Zhang, Y., & Schüler, D. (2016) · Applied and Environmental Microbiology · doi:10.1128/aem.03860-15 · Cited by 60

Integrated Omic Analyses Provide Evidence that a “ Candidatus Accumulibacter phosphatis” Strain Performs Denitrification under Microaerobic Conditions

Camejo, P. Y., Oyserman, B. O., McMahon, K. D., & Noguera, D. R. (2019) · mSystems · doi:10.1128/msystems.00193-18 · Cited by 60

The magnetosome model: insights into the mechanisms of bacterial biomineralization

Rahn-Lee, L., & Komeili, A. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00352 · Cited by 57

New Vectors for Chromosomal Integration Enable High-Level Constitutive or Inducible Magnetosome Expression of Fusion Proteins in Magnetospirillum gryphiswaldense

Borg, S., Hofmann, J. P., Pollithy, A., Lang, C., & Schüler, D. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.00192-14 · Cited by 55

Analysis of Magnetosome Chains in Magnetotactic Bacteria by Magnetic Measurements and Automated Image Analysis of Electron Micrographs

Katzmann, E., Eibauer, M., Lin, W., Pan, Y., Plitzko, J. M., & Schüler, D. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.02143-13 · Cited by 49

Comparative genomic analysis provides insights into the evolution and niche adaptation of marine M agnetospira sp. QH ‐2 strain

Ji, B., Zhang, S., Arnoux, P., Rouy, Z., Alberto, F., Philippe, N., Murat, D., Zhang, W., Rioux, J.-B., Ginet, N., et al. (2013) · Environmental Microbiology · doi:10.1111/1462-2920.12180 · Cited by 48

A Compass To Boost Navigation: Cell Biology of Bacterial Magnetotaxis

Müller, F. D., Schüler, D., & Pfeiffer, D. (2020) · Journal of Bacteriology · doi:10.1128/jb.00398-20 · Cited by 48

Disinfection of water and wastewater by biosynthesized magnetite and zerovalent iron nanoparticles via NAP-NAR enzymes of Proteus mirabilis 10B

Zaki, S. A. E. F., Eltarahony, M. M., & Abd-El-Haleem, D. A. M. (2019) · Environmental Science and Pollution Research · doi:10.1007/s11356-019-05479-2 · Cited by 47

Biomineralization in magnetotactic bacteria: From diversity to molecular discovery-based applications

Wan, J., Ji, R., Liu, J., Ma, K., Pan, Y., & Lin, W. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114995 · Cited by 46

Development of a simple intensified fermentation strategy for growth of Magnetospirillum gryphiswaldense MSR-1: Physiological responses to changing environmental conditions

Fernández‐Castané, A., Li, H., Thomas, O. R. T., & Overton, T. W. (2018) · New Biotechnology · doi:10.1016/j.nbt.2018.05.1201 · Cited by 38

The Terminal Oxidase cbb 3 Functions in Redox Control of Magnetite Biomineralization in Magnetospirillum gryphiswaldense

Li, Y., Raschdorf, O., Silva, K. T., & Schüler, D. (2014) · Journal of Bacteriology · doi:10.1128/jb.01652-14 · Cited by 37

The FtsZ-Like Protein FtsZm of Magnetospirillum gryphiswaldense Likely Interacts with Its Generic Homolog and Is Required for Biomineralization under Nitrate Deprivation

Müller, F. D., Raschdorf, O., Nudelman, H., Messerer, M., Katzmann, E., Plitzko, J. M., Zarivach, R., & Schüler, D. (2013) · Journal of Bacteriology · doi:10.1128/jb.00804-13 · Cited by 37

The oxygen sensor MgFnr controls magnetite biomineralization by regulation of denitrification in Magnetospirillum gryphiswaldense

Li, Y., Sabaty, M., Borg, S., Silva, K. T., Pignol, D., & Schüler, D. (2014) · BMC Microbiology · doi:10.1186/1471-2180-14-153 · Cited by 35

Repeated horizontal gene transfers triggered parallel evolution of magnetotaxis in two evolutionary divergent lineages of magnetotactic bacteria

Monteil, C. L., Grouzdev, D. S., Perrière, G., Alonso, B., Rouy, Z., Cruveiller, S., Ginet, N., Pignol, D., & Lefèvre, C. T. (2020) · The ISME Journal · doi:10.1038/s41396-020-0647-x · Cited by 34

Response to nitrogen addition reveals metabolic and ecological strategies of soil bacteria

Samad, M. S., Johns, C., Richards, K. G., Lanigan, G. J., de Klein, C. A. M., Clough, T. J., & Morales, S. E. (2017) · Molecular Ecology · doi:10.1111/mec.14275 · Cited by 35

Generation of Multifunctional Magnetic Nanoparticles with Amplified Catalytic Activities by Genetic Expression of Enzyme Arrays on Bacterial Magnetosomes

Mickoleit, F., & Schüler, D. (2017) · Advanced Biosystems · doi:10.1002/adbi.201700109 · Cited by 32

Diverse Intracellular Inclusion Types Within Magnetotactic Bacteria: Implications for Biogeochemical Cycling in Aquatic Environments

Li, J., Liu, P., Tamaxia, A., Zhang, H., Liu, Y., Wang, J., Menguy, N., Zhao, X., Roberts, A. P., & Pan, Y. (2021) · Journal of Geophysical Research Biogeosciences · doi:10.1029/2021jg006310 · Cited by 34

Generation of nanomagnetic biocomposites by genetic engineering of bacterial magnetosomes

Mickoleit, F., & Schüler, D. (2018) · Bioinspired Biomimetic and Nanobiomaterials · doi:10.1680/jbibn.18.00005 · Cited by 31

Transposon Mutagenesis Identified Chromosomal and Plasmid Genes Essential for Adaptation of the Marine Bacterium Dinoroseobacter shibae to Anaerobic Conditions

Ebert, M. P. A., Laaß, S., Burghartz, M., Petersen, J., Koßmehl, S., Wöhlbrand, L., Rabus, R., Wittmann, C., Tielen, P., & Jahn, D. (2013) · Journal of Bacteriology · doi:10.1128/jb.00860-13 · Cited by 31

An automated oxystat fermentation regime for microoxic cultivation of Magnetospirillum gryphiswaldense

Riese, C. N., Uebe, R., Rosenfeldt, S., Schenk, A. S., Jérôme, V., Freitag, R., & Schüler, D. (2020) · Microbial Cell Factories · doi:10.1186/s12934-020-01469-z · Cited by 29

Physiological characteristics of Magnetospirillum gryphiswaldense MSR-1 that control cell growth under high-iron and low-oxygen conditions

Wang, Q., Wang, X., Zhang, W., Li, X., Zhou, Y., Li, D., Wang, Y., Tian, J., Jiang, W. Z., Zhang, Z., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-03012-4 · Cited by 29

Transcriptome analysis reveals physiological characteristics required for magnetosome formation in Magnetospirillum gryphiswaldense MSR‐1

Wang, X., Wang, Q., Zhang, Y., Wang, Y., Zhou, Y., Zhang, W., Wen, T., Li, L., Zuo, M.-Q., Zhang, Z., et al. (2016) · Environmental Microbiology Reports · doi:10.1111/1758-2229.12395 · Cited by 29

Single‐step transfer of biosynthetic operons endows a non‐magnetotactic Magnetospirillum strain from wetland with magnetosome biosynthesis

Dziuba, M. V., Zwiener, T., Uebe, R., & Schüler, D. (2020) · Environmental Microbiology · doi:10.1111/1462-2920.14950 · Cited by 28

Exploring the host range for genetic transfer of magnetic organelle biosynthesis

Dziuba, M. V., Müller, F. D., Pósfai, M., & Schüler, D. (2023) · Nature Nanotechnology · doi:10.1038/s41565-023-01500-5 · Cited by 26

Genome-Wide Identification of Essential and Auxiliary Gene Sets for Magnetosome Biosynthesis in Magnetospirillum gryphiswaldense

Silva, K. T., Schüler, M., Mickoleit, F., Zwiener, T., Müller, F. D., Awal, R. P., Weig, A. R., Brachmann, A., Uebe, R., & Schüler, D. (2020) · mSystems · doi:10.1128/msystems.00565-20 · Cited by 24

Magnetotactic Bacteria, Magnetosomes, and Nanotechnology

Bazylinski, D. A., Lefèvre, C. T., & Lower, B. H. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1667-2_3 · Cited by 24

Combined genomic and structural analyses of a cultured magnetotactic bacterium reveals its niche adaptation to a dynamic environment

Araújo, A. C. V., Morillo, V., Cypriano, J. B. S., Teixeira, L. C. R. S., Leão, P., de Lyra, S. S., de Almeida, L. G. P., Bazylinski, D. A., de Vasconcelos, A. T. R., Abreu, F. D. Á., et al. (2016) · BMC Genomics · doi:10.1186/s12864-016-3064-9 · Cited by 23

Recent advances in studies on magnetosome‐associated proteins composing the bacterial geomagnetic sensor organelle

Taoka, A., Eguchi, Y., Shimoshige, R., & Fukumori, Y. (2023) · Microbiology and Immunology · doi:10.1111/1348-0421.13062 · Cited by 20

OxyR controls magnetosome formation by regulating magnetosome island (MAI) genes, iron metabolism, and redox state

Niu, W., Zhang, Y., Liu, J., Wen, T., Miao, T., Basit, A., & Jiang, W. Z. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.10.015 · Cited by 20

Pyrite-Based Autotrophic Denitrifying Microorganisms Derived from Paddy Soils: Effects of Organic Co-Substrate Addition

Xu, B., Xiaoxia, Y., Li, Y., Yang, K., Xiong, Y., & Yuan, N. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph191811763 · Cited by 19

Identification and characterization of magnetotactic Gammaproteobacteria from a salt evaporation pool, Bohai Bay, China

Liu, P., Tamaxia, A., Liu, Y., Qiu, H., Pan, J., Jin, Z., Zhao, X., Roberts, A. P., Pan, Y., & Li, J. (2021) · Environmental Microbiology · doi:10.1111/1462-2920.15516 · Cited by 19

Nitric oxide sensor NsrR is the key direct regulator of magnetosome formation and nitrogen metabolism in Magnetospirillum

Pang, B., Zheng, H., Ma, S., Tian, J., & Wen, Y. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkad1230 · Cited by 18

A magnetosome-associated cytochrome MamP is critical for magnetite crystal growth during the exponential growth phase

Taoka, A., Eguchi, Y., Mise, S., Oestreicher, Z., Uno, F., & Fukumori, Y. (2014) · FEMS Microbiology Letters · doi:10.1111/1574-6968.12541 · Cited by 18

Quantifying the Benefit of a Dedicated “Magnetoskeleton” in Bacterial Magnetotaxis by Live-Cell Motility Tracking and Soft Agar Swimming Assay

Pfeiffer, D., & Schüler, D. (2019) · Applied and Environmental Microbiology · doi:10.1128/aem.01976-19 · Cited by 18

Changes of cell growth and magnetosome biomineralization in Magnetospirillum magneticum AMB-1 after ultraviolet-B irradiation

Wang, Y.-Z., Lin, W., Li, J., & Pan, Y.-X. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00397 · Cited by 20

Biosynthesis and function of magnetic organelles in magnetotactic bacteria

Schüler, D., Dziuba, M. V., Pfeiffer, D., & Uebe, R. (2025) · Nature Reviews Microbiology · doi:10.1038/s41579-025-01234-2 · Cited by 16

Large-Scale Cultivation of Magnetotactic Bacteria and the Optimism for Sustainable and Cheap Approaches in Nanotechnology

Cabral, A. D. S., Verdan, M., Presciliano, R., Silveira, F., Corrêa, T., & Abreu, F. D. Á. (2023) · Marine Drugs · doi:10.3390/md21020060 · Cited by 16

Substrate-mediated trade-offs between pollutant removal efficiency and ecological risks in constructed wetlands treating multi-antibiotic wastewater

Hu, X., Huo, J., Yue, J., Hu, Z., Xie, H., & Zhang, J. (2026) · Water Research · doi:10.1016/j.watres.2026.125414 · Cited by 15

High‐Yield Production, Characterization, and Functionalization of Recombinant Magnetosomes in the Synthetic Bacterium Rhodospirillum rubrum “magneticum”

Mickoleit, F., Rosenfeldt, S., Toro‐Nahuelpan, M., Schaffer, M., Schenk, A. S., Plitzko, J. M., & Schüler, D. (2021) · Advanced Biology · doi:10.1002/adbi.202101017 · Cited by 15

Calcite and Vaterite Biosynthesis by Nitrate Dissimilating Bacteria in Carbonatogenesis Process under Aerobic and Anaerobic Conditions

Eltarahony, M. M., Zaki, S. A. E. F., Kamal, A., & Abd-El-Haleem, D. A. M. (2021) · Geomicrobiology Journal · doi:10.1080/01490451.2021.1951398 · Cited by 15

The transcriptomic landscape of Magnetospirillum gryphiswaldense during magnetosome biomineralization

Riese, C. N., Wittchen, M., Jérôme, V., Freitag, R., Busche, T., Kalinowski, J., & Schüler, D. (2022) · BMC Genomics · doi:10.1186/s12864-022-08913-x · Cited by 14

Therapeutic and antioxidant potential of bionanofactory Ochrobactrum sp.-mediated magnetite and zerovalent iron nanoparticles against acute experimental toxoplasmosis

Hezema, N. N., Eltarahony, M. M., & Salam, S. A. A. (2023) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0011655 · Cited by 14

Analysis of Zobellella denitrificans ZD1 draft genome: Genes and gene clusters responsible for high polyhydroxybutyrate (PHB) production from glycerol under saline conditions and its CRISPR-Cas system

Wu, Y., Yang, S.-H., Hwangbo, M., & Chu, K. (2019) · PLoS ONE · doi:10.1371/journal.pone.0222143 · Cited by 14

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Ji, R., Wan, J., Liu, J., Zheng, J., Xiao, T., Pan, Y., & Lin, W. (2024) · Microbiome · doi:10.1186/s40168-024-01837-6 · Cited by 13

A Versatile Magnetic Nanoplatform for Plug-and-Play Functionalization: Genetically Programmable Cargo Loading to Bacterial Magnetosomes by SpyCatcher “Click Biology”

Mickoleit, F., Beierl, J. J., Markert, S., Klein, M. A., Stäbler, S. Y., Maier, D. S., & Schüler, D. (2024) · ACS Nano · doi:10.1021/acsnano.4c05588 · Cited by 13

Microbe‐mineral biogeography from multi‐year incubations in oceanic crust at North Pond, Mid‐Atlantic Ridge

Orcutt, B. N., D’Angelo, T., Wheat, C. G., & Trembath‐Reichert, E. (2020) · Environmental Microbiology · doi:10.1111/1462-2920.15366 · Cited by 13

Redox control of magnetosome biomineralization

Li, Y. (2021) · Journal of Oceanology and Limnology · doi:10.1007/s00343-021-0422-5 · Cited by 13

Construction of Recombinant Magnetospirillum Strains for Nitrate Removal from Wastewater Based on Magnetic Adsorption

Zheng, H., Pang, B., Pang, B., Ma, S., Ma, S., Xu, J., Wen, Y., & Tian, J. (2022) · Processes · doi:10.3390/pr10030591 · Cited by 12

Controlled Biomineralization of Magnetite in Bacteria

Descamps, E. C. T., Abbé, J., Pignol, D., & Lefèvre, C. T. (2016) · doi:10.1002/9783527691395.ch5 · Cited by 11

Effects of culture conditions on denitrification activity by Magnetospirillum gryphiswaldense strain MSR-1

Hu, J., Yang, W., Li, L., & Liu, Y. (2022) · Journal of Water Process Engineering · doi:10.1016/j.jwpe.2022.103316 · Cited by 10

Genomic features of “Candidatus Venteria ishoeyi”, a new sulfur-oxidizing macrobacterium from the Humboldt Sulfuretum off Chile

Fonseca, A., Ishoey, T., Espinoza, C., Pérez-Pantoja, D. R., Manghisi, A., Morabito, M., Salas-Burgos, A., & Gallardo, V. A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0188371 · Cited by 10

The synthesis of iron oxide nanoparticles in confined space

Zhao, Y., Wu, L., Li, Y., Mao, Y., & Gu, N. (2024) · Science China Materials · doi:10.1007/s40843-024-2875-3 · Cited by 8

Novel Protein Mg2046 Regulates Magnetosome Synthesis in Magnetospirillum gryphiswaldense MSR-1 by Modulating a Proper Redox Status

Wang, X., Zheng, H., Wang, Q., Jiang, W. Z., Wen, Y., Tian, J., Sun, J., Li, Y., & Li, J. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01478 · Cited by 9

A Two‐Protein Chemoreceptor Complex Regulates Oxygen Thresholds in Bacterial Magneto‐Aerotaxis

Herz, J., Weigel, C., Scheder, L., Zarivach, R., Algov, I., Chemla, Y., Popp, F., Riese, C. N., Charsooghi, M. A., Alfonta, L., et al. (2025) · Advanced Science · doi:10.1002/advs.202417315 · Cited by 7

Assessing the effects of NapA gene overexpression on denitrification and denitrogenation in magnetospirillum gryphiswaldense MSR-1

Hu, J., Liu, M., Li, L., Hu, J., & Wang, C. (2024) · Archives of Microbiology · doi:10.1007/s00203-024-04158-2 · Cited by 7

Biosynthesis and Intracellular Organization of Magnetosomes in Magnetotactic Bacteria

Schüler, D., & Müller, F. D. (2020) · Microbiology monographs · doi:10.1007/978-3-030-60173-7_3 · Cited by 7

Genetic engineered molecular imaging probes for applications in cell therapy: emphasis on MRI approach.

Cho, I. K., Wang, S., Mao, H. Z., & Chan, A. W. S. (2016) · Europe PMC (PubMed Central) · Cited by 7

Global Analysis of Biomineralization Genes in Magnetospirillum magneticum AMB-1

McCausland, H. C., Wetmore, K. M., Arkin, A. P., & Komeili, A. (2022) · mSystems · doi:10.1128/msystems.01037-21 · Cited by 7

Effects of static magnetic field on the sulfate metabolic pathway involved in Magnetospirillum magneticum AMB-1 cell growth and magnetosome formation

Chen, H., Shi, H., Chen, C., Jiao, Y., Wang, P., Chen, C., Li, J., Wu, L., & Song, T. (2023) · Journal of Applied Microbiology · doi:10.1093/jambio/lxad302 · Cited by 6

Magnetochrome-catalyzed oxidation of ferrous iron by MamP enables magnetite crystal growth in the magnetotactic bacterium AMB-1

Amor, M., Chevrier, D. M., Siponen, M. I., Egli, R., Scoppola, E., Marcano, L., Li, C., Choueikani, F., & Faivre, D. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2410245121 · Cited by 6

Marine Biominerals with a Biotechnological Future

Barre, S., & Bates, S. S. (2018) · Blue Biotechnology · doi:10.1002/9783527801718.ch27 · Cited by 6

Biochar incorporation to paddy soils increased Cd accumulation in rice grains through priming effects of rhizosphere microorganisms

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