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Bacterial chemolithoautotrophy via manganese oxidation

  • 1.

    Beijerinck, M. Oxydation des mangancarbonates durch Bakterien und Schimmelpilze. Folia Microbiol. (Delft) 2, 123–134 (1913).

    Google Scholar 

  • 2.

    Nealson, K. H., Tebo, B. M. & Rosson, R. A. Occurrence and mechanisms of microbial oxidation of manganese. Adv. Appl. Microbiol. 33, 279–318 (1988).

    CAS  Google Scholar 

  • 3.

    Tebo, B. M., Johnson, H. A., McCarthy, J. K. & Templeton, A. S. Geomicrobiology of manganese(II) oxidation. Trends Microbiol. 13, 421–428 (2005).

    CAS  Google Scholar 

  • 4.

    Hansel, C. & Learman, D. R. in Ehrlich’s Geomicrobiology (eds Ehrlich, H. L. et al.) 401–452 (CRC, 2015).

  • 5.

    Myers, C. R. & Nealson, K. H. Bacterial manganese reduction and growth with manganese oxide as the sole electron acceptor. Science 240, 1319–1321 (1988).

    ADS  CAS  Google Scholar 

  • 6.

    Lovley, D. R. & Phillips, E. J. Novel mode of microbial energy metabolism: organic carbon oxidation coupled to dissimilatory reduction of iron or manganese. Appl. Environ. Microbiol. 54, 1472–1480 (1988).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 7.

    Winogradsky, S. Über schwefelbakterien. Bot. Ztg 45, 489ff (1887).

    Google Scholar 

  • 8.

    Kelly, D. P. & Wood, A. P. in The Prokaryotes: Prokaryotic Communities and Ecophysiology (eds Rosenberg, E. et al.) 275–287 (Springer, 2013).

  • 9.

    Daims, H. et al. Complete nitrification by Nitrospira bacteria. Nature 528, 504–509 (2015).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  • 10.

    Könneke, M. et al. Isolation of an autotrophic ammonia-oxidizing marine archaeon. Nature 437, 543–546 (2005).

    ADS  Google Scholar 

  • 11.

    Strous, M. et al. Missing lithotroph identified as new planctomycete. Nature 400, 446–449 (1999).

    ADS  CAS  Google Scholar 

  • 12.

    van Kessel, M. A. H. J. et al. Complete nitrification by a single microorganism. Nature 528, 555–559 (2015).

    ADS  PubMed  PubMed Central  Google Scholar 

  • 13.

    Watson, S. W. & Waterbury, J. B. Characteristics of two marine nitrite oxidizing bacteria, Nitrospina gracilis nov. gen. nov. sp. and Nitrococcus mobilis nov. gen. nov. sp. Arch. Mikrobiol. 77, 203–230 (1971).

    Google Scholar 

  • 14.

    Lovley, D. R., Holmes, D. E. & Nevin, K. P. in Advances in Microbial Physiology (ed Poole, R. K.) 219–286 (Elsevier, 2004).

  • 15.

    Henkel, J. V. et al. A bacterial isolate from the Black Sea oxidizes sulfide with manganese(IV) oxide. Proc. Natl Acad. Sci. USA 116, 12153–12155 (2019).

    CAS  Google Scholar 

  • 16.

    Ghiorse, W. C. & Ehrlich, H. L. Microbial biomineralization of iron and manganese. Catena Suppl. 21, 75–99 (1992).

    Google Scholar 

  • 17.

    Ehrlich, H. L. & Salerno, J. C. Energy coupling in Mn2+ oxidation by a marine bacterium. Arch. Microbiol. 154, 12–17 (1990).

    CAS  Google Scholar 

  • 18.

    Ehrlich, H. L. Manganese as an energy source for bacteria. Environ. Biogeochem. 2, 633–644 (1976).

    CAS  Google Scholar 

  • 19.

    Dick, G. J. et al. Genomic insights into Mn(II) oxidation by the marine alphaproteobacterium Aurantimonas sp. strain SI85-9A1. Appl. Environ. Microbiol. 74, 2646–2658 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 20.

    Nealson, K. H. in The Prokaryotes (eds Dworkin, M. et al.) 222–231 (Springer, 2006).

  • 21.

    van Veen, W. L. Biological oxidation of manganese in soils. Antonie van Leeuwenhoek 39, 657–662 (1973).

    Google Scholar 

  • 22.

    Morgan, J. J. Kinetics of reaction between O2 and Mn(II) species in aqueous solutions. Geochim. Cosmochim. Acta 69, 35–48 (2005).

    ADS  CAS  Google Scholar 

  • 23.

    Kits, K. D. et al. Kinetic analysis of a complete nitrifier reveals an oligotrophic lifestyle. Nature 549, 269–272 (2017).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  • 24.

    Flagan, S. F. & Leadbetter, J. R. Utilization of capsaicin and vanillylamine as growth substrates by Capsicum (hot pepper)-associated bacteria. Environ. Microbiol. 8, 560–565 (2006).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 25.

    Kanzler, B. E. M., Pfannes, K. R., Vogl, K. & Overmann, J. Molecular characterization of the nonphotosynthetic partner bacterium in the consortium “Chlorochromatium aggregatum”. Appl. Environ. Microbiol. 71, 7434–7441 (2005).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 26.

    Emerson, D. & Moyer, C. Isolation and characterization of novel iron-oxidizing bacteria that grow at circumneutral pH. Appl. Environ. Microbiol. 63, 4784–4792 (1997).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 27.

    Neidhardt, F. C. Escherichia coli and Salmonella: Cellular and Molecular Biology, vol. 1 (ASM, 1996).

  • 28.

    Kostanjšek, R., Pašić, L., Daims, H. & Sket, B. Structure and community composition of sprout-like bacterial aggregates in a dinaric karst subterranean stream. Microb. Ecol. 66, 5–18 (2013).

    Google Scholar 

  • 29.

    Wrighton, K. C. et al. Fermentation, hydrogen, and sulfur metabolism in multiple uncultivated bacterial phyla. Science 337, 1661–1665 (2012).

    ADS  CAS  Google Scholar 

  • 30.

    Parks, D. H. et al. Recovery of nearly 8,000 metagenome-assembled genomes substantially expands the tree of life. Nat. Microbiol. 2, 1533–1542 (2017).

    CAS  Google Scholar 

  • 31.

    Castelle, C. et al. A new iron-oxidizing/O2-reducing supercomplex spanning both inner and outer membranes, isolated from the extreme acidophile Acidithiobacillus ferrooxidans. J. Biol. Chem. 283, 25803–25811 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 32.

    Jeans, C. et al. Cytochrome 572 is a conspicuous membrane protein with iron oxidation activity purified directly from a natural acidophilic microbial community. ISME J. 2, 542–550 (2008).

    CAS  Google Scholar 

  • 33.

    Croal, L. R., Jiao, Y. & Newman, D. K. The fox operon from Rhodobacter strain SW2 promotes phototrophic Fe(II) oxidation in Rhodobacter capsulatus SB1003. J. Bacteriol. 189, 1774–1782 (2007).

    CAS  Google Scholar 

  • 34.

    Jiao, Y. & Newman, D. K. The pio operon is essential for phototrophic Fe(II) oxidation in Rhodopseudomonas palustris TIE-1. J. Bacteriol. 189, 1765–1773 (2007).

    CAS  Google Scholar 

  • 35.

    He, S., Barco, R. A., Emerson, D. & Roden, E. E. Comparative genomic analysis of neutrophilic iron(II) oxidizer genomes for candidate genes in extracellular electron transfer. Front. Microbiol. 8, 1584 (2017).

    PubMed  PubMed Central  Google Scholar 

  • 36.

    Richardson, D. J. et al. The ‘porin-cytochrome’ model for microbe-to-mineral electron transfer. Mol. Microbiol. 85, 201–212 (2012).

    CAS  Google Scholar 

  • 37.

    Luther, G. W., III. Manganese(II) oxidation and Mn(IV) reduction in the environment—two one-electron transfer steps versus a single two-electron Step. Geomicrobiol. J. 22, 195–203 (2005).

    CAS  Google Scholar 

  • 38.

    Lücker, S. et al. A Nitrospira metagenome illuminates the physiology and evolution of globally important nitrite-oxidizing bacteria. Proc. Natl Acad. Sci. USA 107, 13479–13484 (2010).

    ADS  Google Scholar 

  • 39.

    Mundinger, A. B., Lawson, C. E., Jetten, M. S. M., Koch, H. & Lücker, S. Cultivation and transcriptional analysis of a canonical Nitrospira under stable growth conditions. Front. Microbiol. 10, 1325 (2019).

    PubMed  PubMed Central  Google Scholar 

  • 40.

    Koch, H. et al. Growth of nitrite-oxidizing bacteria by aerobic hydrogen oxidation. Science 345, 1052–1054 (2014).

    ADS  CAS  Google Scholar 

  • 41.

    Levicán, G., Ugalde, J. A., Ehrenfeld, N., Maass, A. & Parada, P. Comparative genomic analysis of carbon and nitrogen assimilation mechanisms in three indigenous bioleaching bacteria: predictions and validations. BMC Genomics 9, 581 (2008).

    PubMed  PubMed Central  Google Scholar 

  • 42.

    Berg, I. A. Ecological aspects of the distribution of different autotrophic CO2 fixation pathways. Appl. Environ. Microbiol. 77, 1925–1936 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 43.

    Thauer, R. K., Jungermann, K. & Decker, K. Energy conservation in chemotrophic anaerobic bacteria. Bacteriol. Rev. 41, 100–180 (1977).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 44.

    Baradaran, R., Berrisford, J. M., Minhas, G. S. & Sazanov, L. A. Crystal structure of the entire respiratory complex I. Nature 494, 443–448 (2013).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  • 45.

    Chadwick, G. L., Hemp, J., Fischer, W. W. & Orphan, V. J. Convergent evolution of unusual complex I homologs with increased proton pumping capacity: energetic and ecological implications. ISME J. 12, 2668–2680 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 46.

    Lücker, S., Nowka, B., Rattei, T., Spieck, E. & Daims, H. The genome of Nitrospina gracilis illuminates the metabolism and evolution of the major marine nitrite oxidizer. Front. Microbiol. 4, 27 (2013).

    PubMed  PubMed Central  Google Scholar 

  • 47.

    Watson, S. W., Bock, E., Valois, F. W., Waterbury, J. B. & Schlosser, U. Nitrospira marina gen. nov. sp. nov.: a chemolithotrophic nitrite-oxidizing bacterium. Arch. Microbiol. 144, 1–7 (1986).

    Google Scholar 

  • 48.

    Hippe, H. Leptospirillum gen. nov. (ex Markosyan 1972), nom. rev., including Leptospirillum ferrooxidans sp. nov. (ex Markosyan 1972), nom. rev. and Leptospirillum thermoferrooxidans sp. nov. (Golovacheva et al. 1992). Int. J. Syst. Evol. Microbiol. 50, 501–503 (2000).

    Google Scholar 

  • 49.

    Henry, E. A. et al. Characterization of a new thermophilic sulfate-reducing bacterium Thermodesulfovibrio yellowstonii, gen. nov. and sp. nov.: its phylogenetic relationship to Thermodesulfobacterium commune and their origins deep within the bacterial domain. Arch. Microbiol. 161, 62–69 (1994).

    CAS  Google Scholar 

  • 50.

    Lin, X., Kennedy, D., Fredrickson, J., Bjornstad, B. & Konopka, A. Vertical stratification of subsurface microbial community composition across geological formations at the Hanford site. Environ. Microbiol. 14, 414–425 (2012).

    CAS  Google Scholar 

  • 51.

    Flagan, S., Ching, W.-K. & Leadbetter, J. R. Arthrobacter strain VAI-A utilizes acyl-homoserine lactone inactivation products and stimulates quorum signal biodegradation by Variovorax paradoxus. Appl. Environ. Microbiol. 69, 909–916 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 52.

    Leadbetter, J. R. & Greenberg, E. P. Metabolism of acyl-homoserine lactone quorum-sensing signals by Variovorax paradoxus. J. Bacteriol. 182, 6921–6926 (2000).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 53.

    Krumbein, W. E. & Altmann, H. J. A new method for the detection and enumeration of manganese oxidizing and reducing microorganisms. Helgol. Wiss. Meeresunters. 25, 347–356 (1973).

    CAS  Google Scholar 

  • 54.

    Emerson, D. & Revsbech, N. P. Investigation of an iron-oxidizing microbial mat community located near Aarhus, Denmark: laboratory studies. Appl. Environ. Microbiol. 60, 4032–4038 (1994).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 55.

    Parada, A. E., Needham, D. M. & Fuhrman, J. A. Every base matters: assessing small subunit rRNA primers for marine microbiomes with mock communities, time series and global field samples. Environ. Microbiol. 18, 1403–1414 (2016).

    CAS  Google Scholar 

  • 56.

    Illumina. 16S Metagenomic sequencing library preparation, https://support.illumina.com/downloads/16s_metagenomic_sequencing_library_preparation.html (2013).

  • 57.

    Caporaso, J. G. et al. QIIME allows analysis of high-throughput community sequencing data. Nat. Methods 7, 335–336 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 58.

    Edgar, R. C. Search and clustering orders of magnitude faster than BLAST. Bioinformatics 26, 2460–2461 (2010).

    CAS  Google Scholar 

  • 59.

    Quast, C. et al. The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Res. 41, D590–D596 (2013).

    CAS  Google Scholar 

  • 60.

    Lane, D. J. in Nucleic Acid Techniques in Bacterial Systematics (eds Stackebrandt, E. & Goodfellow, M.) 115–175 (John Wiley & Sons, 1991).

  • 61.

    Ludwig, W. et al. ARB: a software environment for sequence data. Nucleic Acids Res. 32, 1363–1371 (2004).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 62.

    Parks, D. H. et al. A standardized bacterial taxonomy based on genome phylogeny substantially revises the tree of life. Nat. Biotechnol. 36, 996–1004 (2018).

    CAS  Google Scholar 

  • 63.

    Schönmann, S. et al. 16S rRNA gene-based phylogenetic microarray for simultaneous identification of members of the genus Burkholderia. Environ. Microbiol. 11, 779–800 (2009).

    Google Scholar 

  • 64.

    Greuter, D., Loy, A., Horn, M. & Rattei, T. probeBase—an online resource for rRNA-targeted oligonucleotide probes and primers: new features 2016. Nucleic Acids Res. 44, D586–D589 (2016).

    CAS  Google Scholar 

  • 65.

    Amann, R. I. et al. Combination of 16S rRNA-targeted oligonucleotide probes with flow cytometry for analyzing mixed microbial populations. Appl. Environ. Microbiol. 56, 1919–1925 (1990).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 66.

    Stoecker, K., Dorninger, C., Daims, H. & Wagner, M. Double labeling of oligonucleotide probes for fluorescence in situ hybridization (DOPE-FISH) improves signal intensity and increases rRNA accessibility. Appl. Environ. Microbiol. 76, 922–926 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 67.

    Schramm, A., Fuchs, B. M., Nielsen, J. L., Tonolla, M. & Stahl, D. A. Fluorescence in situ hybridization of 16S rRNA gene clones (Clone-FISH) for probe validation and screening of clone libraries. Environ. Microbiol. 4, 713–720 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 68.

    Daims, H., Stoecker, K. & Wagner, M. in Molecular Microbial Ecology (eds Osborn, M. A. and Smith, C. J.) 208–228 (Taylor & Francis, 2004).

  • 69.

    Daims, H., Lücker, S. & Wagner, M. daime, a novel image analysis program for microbial ecology and biofilm research. Environ. Microbiol. 8, 200–213 (2006).

    CAS  Google Scholar 

  • 70.

    Taylor, G. J. & Crowder, A. A. Use of the DCB technique for extraction of hydrous iron oxides from roots of wetland plants. Am. J. Bot. 70, 1254 (1983).

    CAS  Google Scholar 

  • 71.

    Polerecky, L. et al. Look@NanoSIMS—a tool for the analysis of nanoSIMS data in environmental microbiology. Environ. Microbiol. 14, 1009–1023 (2012).

    CAS  Google Scholar 

  • 72.

    Brewer, P. G. & Spencer, D. W. Colorimetric determination of manganse in anoxic waters. Limnol. Oceanogr. 16, 107–110 (1971).

    ADS  CAS  Google Scholar 

  • 73.

    Oldham, V. E., Miller, M. T., Jensen, L. T. & Luther, G. W. Revisiting Mn and Fe removal in humic rich estuaries. Geochim. Cosmochim. Acta 209, 267–283 (2017).

    ADS  CAS  Google Scholar 

  • 74.

    Suzuki, M. T., Taylor, L. T. & DeLong, E. F. Quantitative analysis of small-subunit rRNA genes in mixed microbial populations via 5′-nuclease assays. Appl. Environ. Microbiol. 66, 4605–4614 (2000).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 75.

    William, S., Feil, H. & Copeland, A. Bacterial genomic DNA isolation using CTAB, Department of Energy Joint Genome Institute, https://jgi.doe.gov/user-programs/pmo-overview/protocols-sample-preparation-information/ (2012).

  • 76.

    Arkin, A. P. et al. KBase: the United States Department of Energy systems biology knowledgebase. Nat. Biotechnol. 36, 566–569 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 77.

    Bolger, A. M., Lohse, M. & Usadel, B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 30, 2114–2120 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 78.

    Bankevich, A. et al. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J. Comput. Biol. 19, 455–477 (2012).

    MathSciNet  CAS  PubMed  PubMed Central  Google Scholar 

  • 79.

    Karst, S. M., Kirkegaard, R. H. & Albertsen, M. mmgenome: a toolbox for reproducible genome extraction from metagenomes. Preprint at https://www.biorxiv.org/content/ 10.1101/059121v1.full (2016).

  • 80.

    Langmead, B. & Salzberg, S. L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 9, 357–359 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 81.

    Chen, I. A. et al. IMG/M v.5.0: an integrated data management and comparative analysis system for microbial genomes and microbiomes. Nucleic Acids Res. 47, D666–D677 (2019).

    CAS  Google Scholar 

  • 82.

    NCBI Resource Coordinators. Database resources of the National Center for Biotechnology Information. Nucleic Acids Res. 46, D8–D13 (2018).

    Google Scholar 

  • 83.

    Bagos, P. G., Liakopoulos, T. D., Spyropoulos, I. C. & Hamodrakas, S. J. PRED-TMBB: a web server for predicting the topology of β-barrel outer membrane proteins. Nucleic Acids Res. 32, W400–W404 (2004).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 84.

    Federhen, S. The NCBI taxonomy database. Nucleic Acids Res. 40, D136–D143 (2012).

    CAS  Google Scholar 

  • 85.

    Parks, D. H., Imelfort, M., Skennerton, C. T., Hugenholtz, P. & Tyson, G. W. CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res. 25, 1043–1055 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 86.

    Pruesse, E., Peplies, J. & Glöckner, F. O. SINA: accurate high-throughput multiple sequence alignment of ribosomal RNA genes. Bioinformatics 28, 1823–1829 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 87.

    Ronquist, F. et al. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst. Biol. 61, 539–542 (2012).

    PubMed  PubMed Central  Google Scholar 

  • 88.

    Letunic, I. & Bork, P. Interactive tree of life (iTOL) v3: an online tool for the display and annotation of phylogenetic and other trees. Nucleic Acids Res. 44, W242–W245 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 89.

    Stamatakis, A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics 30, 1312–1313 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 90.

    Sievers, F. et al. Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega. Mol. Syst. Biol. 7, 539 (2011).

    PubMed  PubMed Central  Google Scholar 

  • 91.

    Lever, M. A. et al. A modular method for the extraction of DNA and RNA, and the separation of DNA pools from diverse environmental sample types. Front. Microbiol. 6, 476 (2015).

    PubMed  PubMed Central  Google Scholar 

  • 92.

    Kopylova, E., Noé, L. & Touzet, H. SortMeRNA: fast and accurate filtering of ribosomal RNAs in metatranscriptomic data. Bioinformatics 28, 3211–3217 (2012).

    CAS  Google Scholar 

  • 93.

    Bray, N. L., Pimentel, H., Melsted, P. & Pachter, L. Near-optimal probabilistic RNA-seq quantification. Nat. Biotechnol. 34, 525–527 (2016).

    CAS  PubMed  Google Scholar 

  • 94.

    Pimentel, H., Bray, N. L., Puente, S., Melsted, P. & Pachter, L. Differential analysis of RNA-seq incorporating quantification uncertainty. Nat. Methods 14, 687–690 (2017).

    CAS  Google Scholar 

  • 95.

    van Waasbergen, L. G., Hildebrand, M. & Tebo, B. M. Identification and characterization of a gene cluster involved in manganese oxidation by spores of the marine Bacillus sp. strain SG-1. J. Bacteriol. 178, 3517–3530 (1996).

    PubMed  PubMed Central  Google Scholar 

  • 96.

    Jung, W. K. & Schweisfurth, R. Manganese oxidation by an intracellular protein of a Pseudomonas species. Z. Allg. Mikrobiol. 19, 107–115 (1979).

    CAS  Google Scholar 

  • 97.

    Esteve-Núñez, A., Rothermich, M., Sharma, M. & Lovley, D. Growth of Geobacter sulfurreducens under nutrient-limiting conditions in continuous culture. Environ. Microbiol. 7, 641–648 (2005).

    Google Scholar 

  • 98.

    Neubauer, S. C., Emerson, D. & Megonigal, J. P. Life at the energetic edge: kinetics of circumneutral iron oxidation by lithotrophic iron-oxidizing bacteria isolated from the wetland-plant rhizosphere. Appl. Environ. Microbiol. 68, 3988–3995 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  • 99.

    Nowka, B., Daims, H. & Spieck, E. Comparison of oxidation kinetics of nitrite-oxidizing bacteria: nitrite availability as a key factor in niche differentiation. Appl. Environ. Microbiol. 81, 745–753 (2015).

    PubMed  PubMed Central  Google Scholar 

  • 100.

    Ehrich, S., Behrens, D., Lebedeva, E., Ludwig, W. & Bock, E. A new obligately chemolithoautotrophic, nitrite-oxidizing bacterium, Nitrospira moscoviensis sp. nov. and its phylogenetic relationship. Arch. Microbiol. 164, 16–23 (1995).

    CAS  Google Scholar 

  • 101.

    Kim, S. & Lee, S. B. Catalytic promiscuity in dihydroxy-acid dehydratase from the thermoacidophilic archaeon Sulfolobus solfataricus. J. Biochem. 139, 591–596 (2006).

    CAS  Google Scholar 

  • 102.

    Safarian, S. et al. Structure of a bd oxidase indicates similar mechanisms for membrane-integrated oxygen reductases. Science 352, 583–586 (2016).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  • 103.

    Lovley, D. R. & Phillips, E. J. P. Manganese inhibition of microbial iron reduction in anaerobic sediments. Geomicrobiol. J. 6, 145–155 (1988).

    CAS  Google Scholar 

  • 104.

    Perez-Benito, J. F., Arias, C. & Amat, E. A kinetic study of the reduction of colloidal manganese dioxide by oxalic acid. J. Colloid Interface Sci. 177, 288–297 (1996).

    ADS  CAS  Google Scholar 


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