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Publications

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2016 Žure, M., A. Fernandez-Guerra, C.B. Munn and J. Harder (2016)
Geographic distribution at subspecies resolution level: closely related Rhodopirellula species in European coastal sediments. ISME J. 2016 Nov 1. doi: 10.1038/ismej.2016.123. [Epub ahead of print]
  Weidenweber, S., R. Marmulla, U. Ermler and J. Harder (2016)
X-ray structure of linalool dehydratase/isomerase from Castellaniella defragrans reveals enzymatic alkene synthesis. FEBS Letters 590, 1375-1383, doi: 10.1002/1873-3468.12165
  Strijkstra A, Trautwein K, Roesler S, Feenders C, Danzer D, Riemenschneider U, Blasius B, Rabus R. (2016)
High performance CCD camera system for digitalisation of 2D DIGE gels. Proteomics 16:1975-1979.
  Panschin, I., M. Becher, S. Verbarg, C. Spröer, M. Rohde, M. Schüler, R.I. Amann, J. Harder, B.J. Tindall, R.L. Hahnke (2016)
Description of Gramella forsetii sp. nov., a marine Flavobacteriaceae isolated from North Sea water, and emended description of Gramella gaetbulicola Cho et al. 2011. Int J Syst Evol Microbiol. 2016 Nov 28. doi: 10.1099/ijsem.0.001700. [Epub ahead of print]
  Marmulla, R., B. Šafarić, S. Markert, T. Schweder and J. Harder (2016)
Linalool isomerase, a membrane-anchored enzyme in the anaerobic monoterpene degradation in Thauera linaloolentis 47Lol. BMC Biochemistry 17, 6, doi: 10.1186/s12858-016-0062-0
  Marmulla, R., E.P. Cala, S. Markert, T. Schweder and J. Harder (2016)
The anaerobic linalool metabolism in Thauera linaloolentis 47Lol. BMC Microbiology 16,76, doi: 10.1186/s12866-016-0693-8.
  Laso-Pérez, R., G. Wegener, K. Knittel, F. Widdel, K.J. Harding, V. Krukenberg, D.V. Meier, M. Richter, H.E. Tegetmeyer, D. Riedel, H.H. Richnow, L. Adrian, T. Reemtsma, O.J. Lechtenfeld, and F. Musat (2016)
Thermophilic archaea activate butane via alkyl-coenzyme M formation. Nature 539, 396-401.
  Dörries M, Wöhlbrand L, Kube M, Reinhardt R, Rabus R. (2016)
Genome and catabolic subproteomes of the marine, nutritionally versatile, sulfate-reducing bacterium Desulfococcus multivorans DSM 2059. BMC Genomics 17:918.
  Dörries M, Wöhlbrand L, Rabus R. (2016)
Differential proteomic analysis of the metabolic network of the marine sulfate-reducer Desulfobacterium autotrophicum HRM2. Proteomics 16:2878-2893.
  Avci, B., R.L. Hahnke, M. Chafee, T. Fischer, H. Gruber-Vodicka, H.E. Tegetmeyer, J. Harder, B.M. Fuchs, R.I. Amann and H. Teeling (2016)
Genomic and physiological analyses of ‘Reinekea forsetii’ reveal a versatile opportunistic lifestyle during spring algae blooms. Environmental Microbiology, in press
2015 Žure, M., C.B. Munn, and J. Harder (2015)
Diversity of Rhodopirellula and related planctomycetes in a North Sea coastal sediment employing carB as molecular marker. FEMS Microbiol Lett 362, fnv127.
  Xing, P., R. L. Hahnke, F. Unfried, S. Markert, S. Huang, T. Barbeyron, J. Harder, D. Becher, T. Schweder, F.O. Glöckner, R.I. Amann and H. Teeling (2015)
Niches of two polysaccharide-degrading Polaribacter isolates from the North Sea during a spring diatom bloom. ISME Journal 9, 1410-22, doi: 10.1038/ismej.2014.225
  Rabus, R., S.S. Venceslau, L. Wöhlbrand, G. Voordouw, J.D. Wall, I.A. Pereira (2015)
A post-genomic view of the ecophysiology, catabolism and biotechnological relevance of sulphate-reducing prokaryotes. Adv Microb Physiol 66, 55-321.
  Kizina, J., M. Žure, E. Rhiel, C.B. Munn, M. Richter, J. Harder (2015)
Permanent draft genome of ´Rhodopirellula islandica´strain K833. Marine Genomics 24, 249-251, doi:10.1016/j.margen.2015.07.011
  Kleiner, M., C. Wentrup, T. Holler, G. Lavik, J. Harder, C. Lott, S. Littmann, M.M.M. Kuypers and N. Dubilier (2015)
Use of carbon monoxide and hydrogen by a bacteria–animal symbiosis from seagrass sediments. Environmental Microbiology 17, 5023-35, doi:10.1111/1462-2920.12912
  Jarling R, Kühner S, Basílio Janke E, Gruner A, Drozdowska M, Golding BT, Rabus R, Wilkes H. (2015)
Versatile transformations of hydrocarbons in anaerobic bacteria: substrate ranges and regio- and stereo-chemistry of activation reactions. Front Microbiol 6:880.
  Hahnke, R.L., C.M. Bennke, B.M. Fuchs, A.J. Mann, E. Rhiel, H. Teeling, R.I. Amann and J. Harder (2015)
Dilution cultivation of marine heterotrophic bacteria abundant after a spring phytoplankton bloom in the North Sea. Environmental Microbiology 17, 3515-3526, doi: 10.1111/1462-2920.12479
  Büsing I, Kant M, Dörries M, Wöhlbrand L, Rabus R. (2015b)
The predicted σ(54)-dependent regulator EtpR is essential for expression of genes for anaerobic p-ethylphenol and p-hydroxyacetophenone degradation in "Aromatoleum aromaticum" EbN1. BMC Microbiol 15:251.
  Büsing I, Höffken W, Breuer M, Wöhlbrand L, Hauer B, Rabus R. (2015a)
Molecular genetic and crystal structural analysis of 1-(4-hydroxyphenyl)-ethanol dehydrogenase from "Aromatoleum aromaticum" EbN1. J Mol Microbiol Biotechnol 25:327-339.
  Beese-Vasbender, P.F., J.P. Grote, J. Garrelfs, M. Stratmann and K.J. Mayrhofer (2015) Selective microbial electrosynthesis of methane by a pure culture of a marine lithoautotrophic archaeon. Bioelectrochemistry 102, 50-55.
2014 Wiegmann K, Hensler M, Wöhlbrand L, Ulbrich M, Schomburg D, Rabus R. (2014)
Carbohydrate catabolism in Phaeobacter inhibens DSM 17395, member of the marine Roseobacter clade. Appl Environ Microbiol 80:4725-4737.
  Wegner, C.-E., M. Richter, T. Richter-Heitmann, A. Klindworth, C.S. Frank, F.O. Glöckner, and J. Harder (2014)
Permanent draft genome of Rhodopirellula sallentina SM41. Marine Genomics 13, 17-18.
  Strijkstra A, Trautwein K, Jarling R, Wöhlbrand L, Dörries M, Reinhardt R, Drozdowska M, Golding BT, Wilkes H, Rabus R. (2014)
Anaerobic activation of p-cymene in denitrifying Betaproteobacteria: methyl group hydroxylation versus addition to fumarate. Appl Environ Microbiol 80:7592-7603.
  Richter-Heitmann, T., M. Richter, A. Klindworth, C.-E. Wegner, C.S. Frank, F.O. Glöckner, and J. Harder (2014)
Permanent draft genomes of the two Rhodopirellula europaea strains 6C and SH398. Marine Genomics 13,15-16.
  Richter, M., T. Richter-Heitmann, A. Klindworth, C.-E. Wegner, C.S. Frank, J. Harder, and F.O. Glöckner (2014)
Permanent draft genomes of the three Rhodopirellula baltica strains SH28, SWK14 and WH47. Marine Genomics 13, 13-14.
  Richter, M., T. Richter-Heitmann, A. Klindworth, C.-E. Wegner, C.S. Frank, J. Harder, and F.O. Glöckner  (2014)
Permanent draft genomes of the Rhodopirellula maiorica strain SM1. Marine Genomics 13, 19-20.
  Petasch, J., E.M. Disch, S. Markert, D. Becher, T. Schweder, B. Hüttel, R. Reinhardt and J. Harder (2014)
The oxygen-independent metabolism of cyclic monoterpenes in Castellaniella defragrans 65Phen. BMC Microbiology 14, 164, doi: 10.1186/1471-2180-14-164
  Marmulla R., and J. Harder (2014)
Microbial monoterpene transformations - a review. Frontiers in Microbiology 5:346. doi: 10.3389/fmicb.2014.00346
  Lahme S, Trautwein K, Strijkstra A, Dörries M, Wöhlbrand L, Rabus R. (2014)
Benzoate mediates the simultaneous repression of anaerobic 4-methylbenzoate and succinate utilization in Magnetospillum sp. strain pMbN1. BMC Microbiology 14:269.
  Klindworth, A., M. Richter, T. Richter-Heitmann, C.-E. Wegner, C.S. Frank, F.O. Glöckner, and J. Harder (2014)
Permanent draft genome of Rhodopirellula rubra SWK7. Marine Genomics 13, 11-12.
  Farnelid, H., J. Harder, M. Bentzon-Tilia, L. Riemann (2014)
Isolation of heterotrophic diazotrophic bacteria from estuarine surface waters. Environmental Microbiology 16, 3072-3082, DOI:10.1111/1462-2920.12335
  Drüppel K, Hensler M, Trautwein K, Koßmehl S, Wöhlbrand L, Schmidt-Hohagen K, Ulbrich M, Bergen N, Meier-Kolthoff JP, Göker M, Klenk HP, Schomburg D, Rabus R. (2014)
Pathways and substrate-specific regulation of amino acid degradation in Phaeobacter inhibens DSM 17395 (archetype of the marine Roseobacter clade). Environ Microbiol 16:218-238
  Bondoso, J., L. Albuquerque, A. Lobo-da-Cunha, M.S. da Costa, J. Harder and O.M. Lage (2014)
Rhodopirellula lusitana sp. nov. and Rhodopirellula rubra sp. nov., isolated from the  surface of macroalgae. Systematic and Applied Microbiology 37, 157-164, doi: 10.1016/j.syapm.2013.11.004
  Ameryk, A., R.L. Hahnke, , S. Gromisz, J. Kownacka, M. Zalewski, L. Szymanek, J. Całkiewicz, J. Dunalska and J. Harder (2014)
Bacterial community structure influenced by Coscinodiscus sp. in the Vistula river plume. Oceanologia 56, 825–856.
  Rabus, R, K. Trautwein, and L. Wöhlbrand (2014)
Towards habitat-oriented systems biology of “Aromatoleum aromaticum” EbN1. Chemical sensing, catabolic network modulation and growth control in anaerobic aromatic compound degradation. Appl. Microbiol. Biotechnol, in press.
  Jaekel, U., C. Vogt, A. Fischer, H.H. Richnow, and F. Musat (2014)
Carbon and hydrogen stable isotope fractionation associated with the anaerobic degradation of propane and butane by marine sulfate-reducing bacteria. Environ. Microbiol. 16, 130–140
  Enning, D., and J. Garrelfs (2014)
Corrosion of iron by sulfate-reducing bacteria: New views of an old problem. Appl. Environ. Microbiol. 80, 1226–1236.
2013

Zech, H., M. Hensler, S. Koßmehl, K. Drüppel, L. Wöhlbrand, K. Trautwein, R. Hulsch, U. Maschmann, T. Colby, J. Schmidt, R. Reinhardt, K. Schmidt-Hohagen, D. Schomburg, and R. Rabus (2013)
Adaptation of Phaeobacter inhibens DSM 17395 to growth with complex nutrients. Proteomics 13, 2851–2868.

 

Wöhlbrand, L., K. Trautwein, and R. Rabus (2013)
Proteomic tools for environmental microbiology-A roadmap from sample preparation to protein identification and quantification. Proteomics 13, 2700–2730.

  Wegner, C.-E., T. Richter-Heitmann, A. Klindworth, C. Klockow, M. Richter, T. Achstetter, F.O. Glöckner, and J. Harder (2013)
Expression of sulfatases in Rhodopirellula baltica and the diversity of sulfatases in the genus Rhodopirellula. Marine Genomics 9, 51–61.
  Spring, S., T. Riedel, C. Spröer, S. Yan, J. Harder, and B.M. Fuchs (2013)
Taxonomy and evolution of bacteriochlorophyll a-containing members of the OM60/NOR5 clade of marine Gammaproteobacteria: Description of Luminiphilus syltensis gen. nov., sp. nov., reclassification of Haliea rubra as Pseudohaliea rubra gen. nov., comb. nov., and emendation of Chromatocurvus halotolerans. BMC Microbiol.13, 118.
  Rabus R. (2013)
Editorial – Environmental microbial proteomics: new avenues for a molecular understanding of the functional role of microorganisms in the natural environment. Proteomics 13, 2697–2699.
  Milucka, J., F. Widdel, and S. Shima (2013)
Immunological detection of enzymes for sulfate reduction in anaerobic methane-oxidizing consortia. Environ. Microbiol. 15, 1561–1571.
  Mann, A.J., R.L. Hahnke, S. Huang, J. Werner, P. Xing, T. Barbeyron, B. Huettel, K. Stüber, R. Reinhardt, J. Harder, F.O. Glöckner, R.I. Amann, and H. Teeling (2013)
The genome of the algae-associated marine flavobacterium Formosa agariphila KMM 3901T reveals a broad potential for the degradation of algal polysaccharides. Appl. Environ. Microbiol. 79, 6813–6822.
  Koßmehl, S., L. Wöhlbrand, K. Drüppel, C. Feenders, B. Blasius, and R. Rabus (2013)
Subcellular protein localization (cell envelope) in Phaeobacter inhibens DSM 17395. Proteomics 13, 2743–2760.
  Hahnke, R.L., C. Probian, B.M. Fuchs, and J. Harder (2013)
Variations in pelagic bacterial communities in the North Atlantic Ocean coincide with water bodies. Aquatic Microbial Ecol. 71, 131–140.
  Hahnke, R.L., and J. Harder (2013) Phylogenetic diversity of Flavobacteria isolated from the North Sea on solid media. Systematic and Applied Microbiology 36, 497–504.
  Frank, C.S.,C. Klockow, M. Richter, F.O. Glöckner, and J. Harder (2013)
Genetic diversity of Rhodopirellula strains. Antonie van Leeuwenhoek 104, 547–550.
  Ebert, M., S. Laaß, M. Burghartz, J. Petersen, S. Koßmehl, L. Wöhlbrand, R. Rabus, C. Wittmann, P. Tielen, and D. Jahn (2013)
Transposon mutagenesis identified chromosomal and plasmid genes essential for adaptation of the marine bacterium Dinoroseobacter shibae to anaerobic conditions. J Bacteriol 195:4769–4777.
  Drüppel, K., M. Hensler, K. Trautwein, S. Koßmehl, L. Wöhlbrand, K. Schmidt-Hohagen, M. Ulbrich, N. Bergen, J.P. Meier-Kolthoff, M. Göker, H.P. Klenk, D. Schomburg, and R. Rabus (2013)
Pathways and substrate-specific regulation of amino acid degradation in Phaeobacter inhibens DSM 17395 (archetype of the marine Roseobacter clade). Environ. Microbiol. doi: 10.1111/1462-2920.12276.
   Bondoso, J., J. Harder, and O.M. Lage (2013)
rpoB gene as a novel marker to infer phylogeny in Planctomycetales. Antonie van Leeuwenhoek 104, 477–488.
 2012 Wolfsheimer, S., A. Hartmann, R. Rabus, and G. Nuel (2012)
Computing posterior probabilities for score-based alignments using ppALIGN. Stat. Appl. Gene. Mol. Biol. 11, Article 1. doi: 10.1515/1544–6115.1702
  Steinbach, A., S. Fraas, J. Harder, E. Warkentin, P. Kroneck, and U. Ermler (2012)
Crystal structure of a ring-cleaving cyclohexane-1,2-dione hydrolase, a novel member of the thiamine diphosphate enzyme family. FEBS J. 279, 1209–1219.
  Lüddeke, F., A. Wülfing, M. Timke, F. Germer, J. Weber, A. Dikfidan, T. Rahnfeld, D. Linder, A. Meyerdierks, and J. Harder (2012)
Geraniol and geranial dehydrogenases induced in anaerobic monoterpene degradation by Castellaniella defragrans. Applied Environmental Microbiology 78, 2128–2136.
  Lüddeke, F., A. Dikfidan, and J. Harder (2012)
Physiology of deletion mutants in the anaerobic β-myrcene degradation pathway in Castellaniella defragrans. BMC Microbiol. 12, 192.
  Lenk, S., C. Moraru, S. Hahnke, J. Arnds, M. Richter, M. Kube, R. Reinhardt, T. Brinkhoff, J. Harder, R. Amann, and M. Mußmann (2012)
Roseobacter clade bacteria are abundant in coastal sediments and encode a novel combination of sulfur oxidation genes. ISME J. 6, 2178–2187.
  Harder, J. (2012)
Vielfalt der marinen Mikroorganismen. In: E. Beck . Hrsg. Die Vielfalt des Lebens. Wiley-VCH, Weinheim.
  Halder T, and R. Rabus (2012)
Dynamik kataboler Netzwerke in Umweltbakterien. Anpassung an wechselnde Umwelt (Nährstoff)bedingungen entschlüsselt durch quantitative Massenspektrometrie. Systembiologie.de 4, 58–61.
  Alain, K., J. Harder, F. Widdel, and K. Zengler (2012)
Anaerobic utilization of toluene by marine alpha- and gammaproteobacteria reducing nitrate. Microbiol. 158, 2946–2957.
  Enning D, Venzlaff H, Garrelfs J, Dinh HT, Meyer V, Mayrhofer K, Hassel AW, Stratmann M and Widdel F (2012)
Marine sulfate-reducing bacteria cause serious corrosion of iron under electroconductive biogenic mineral crust.
Environ Microbiol 14: 1772-1787
DOI: 10.1111/j.1462-2920.2012.02778.x
  Holler T, Wegener G, Niemann H, Deusner C, Ferdelman TG, Boetius A, Brunner B and Widdel F (2012)
Carbon and sulfur back flux during anaerobic microbial oxidation of methane and coupled sulfate reduction.
Proc Natl Acad Sci USA 108: E1484-E1490
DOI: 10.1073/pnas.1106032108
  Jarling R, Sadeghi M, Drozdowska M, Lahme S, Buckel W, Rabus R, Widdel F, Golding BT and Wilkes H (2012)
Stereochemical investigations reveal the mechanism of the bacterial activation of n-alkanes without oxygen.
Angew Chem Int Ed Engl 51: 1334-1338
DOI: 10.1002/anie.201106055
  Jaekel U, Musat N, Adam B, Kuypers M, Grundmann O and Musat F (2012)
Anaerobic degradation of propane and butane by sulfate-reducing bacteria enriched from marine hydrocarbon cold seeps.
ISME J.
doi: 10.1038/ismej (20129)
  Kube M, Mitrovic J, Duduk B, Rabus R and Seemüller E (2012)
Current view on phytoplasma genomes and encoded metabolism.
ScientificWorldJournal: 185942
DOI: 10.1100/2012/185942
  Lahme S, Eberlein C, Jarling R, Kube M, Boll M, Wilkes H, Reinhardt R and Rabus R (2012)
Anaerobic degradation of 4-methylbenzoate via a specific 4-methylbenzoyl-CoA pathway.
Environ Microbiol 14: 1118-1132
DOI: 10.1111/j.1462-2920.2011.02693.x
  Milucka J, Ferdelman TG, Polerecky L, Franzke D, Wegener G, Schmid M, Lieberwirth I, Wagner M, Widdel F and Kuypers MM (2012)
Zero-valent sulphur is a key intermediate in marine methane oxidation.
Nature 491:541-546
DOI: 10.1038/nature11656
  Milucka J, Widdel F and Shima S (2012)
Immunological detection of enzymes for sulfate reduction in anaerobic methane-oxidizing consortia.
Environ Microbiol.
doi: 10.1111/1462-2920.12003
  Rabus R (2012)
An overview of 2D DIGE analysis of marine (environmental) bacteria.
Methods Mol Biol 854: 355-372
DOI: 10.1007/978-1-61779-573-2_25
  Rabus R, Jarling R, Lahme S, Kühner S, Heider J, Widdel F and Wilkes H (2012)
Co-metabolic conversion of toluene in anaerobic n-alkane-degrading bacteria.
Environ Microbiol 13: 2576-2586
DOI: 10.1111/j.1462-2920.2011.02529.x
  Trautwein K, Grundmann O, Wöhlbrand L, Eberlein C, Boll M and Rabus R (2012)
Benzoate mediates repression of C4-dicarboxylate utilization in Aromatoleum aromaticum EbN1.
J Bacteriol 194: 518-528
DOI: 10.1128/JB.05072-11
  Trautwein K, Wilkes H and Rabus R (2012)
Proteogenomic evidence for β-oxidation of plant-derived 3-phenylpropanoids in Aromatoleum aromaticum EbN1.
Proteomics 12: 1402-1413
DOI: 10.1002/pmic.201100279
  Venzlaff H, Enning D, Srinivasan J, Mayrhofer K, Hassel AW, Widdel F and Stratmann M (2012)
Accelerated cathodic reaction in microbial corrosion of iron due to direct electron uptake by sulphate-reducing bacteria.
Corros. Sci.,
doi: 10.1016/j.corsci.2012.09.006
  Wöhlbrand L, Kube M, Mussmann M, Jarling R, Beck A, Amann R, Wilkes H, Reinhardt R and Rabus R (2012)
Complete genome, catabolic sub-proteomes and key-metabolites of Desulfobacula toluolica Tol2, a marine, aromatic compound-degrading, sulfate-reducing bacterium.
Environ Microbiol.
doi: 10.1111/j.1462-2920.2012.02885.x
  Zech H, Echtermeyer C, Wöhlbrand L, Blasius B and Rabus R (2012)
Biological versus technical variability in 2-D DIGE experiments with environmental bacteria.
Proteomics 11: 3380-3389. (Erratum: Proteomics, 2011, 11:3942)
DOI: 10.1002/pmic.201100071
2011 Basen M, Krüger M, Milucka J, Kuever J, Kahnt J, Grundmann O, Meyerdierks A, Widdel F and Seigo Shima S (2011)
Bacterial enzymes for dissimilatory sulfate reduction in a marine microbial mat (Black Sea) mediating anaerobic oxidation of methane.
Environ. Microbiol.,
DOI: 10.1111/j.1462-2920.2011.02443.x
  Frank C S, Langhammer P, Fuchs B M and Harder J (2011)
Ammonia and attachment of Rhodopirellula baltica.
Archives of Microbiology 193: 365−372
DOI: 10.1007/s00203-011-0681-1
  Holler T, Widdel F, Knittel K, Amann R, Kellermann M Y, Hinrichs K-U, Teske A , Boetius A and Wegener G (2011)
Thermophilic anaerobic oxidation of methane by marine microbial consortia
ISME J. 5, 1946–1956
DOI: 10.1038/ismej.2011.77
  Jarling R, Sadeghi M, Drozdowska M, Lahme S, Buckel W, Rabus R, Widdel F, Golding B T and Wilkes H (2011)
Stereochemical investigations reveal the mechanism of the bacterial activation of n-alkanes without oxygen.
Angew Chem Int Ed,
DOI: 10.1002/anie.201106055
  Lahme S, Harder J and Rabus R (2011)
Anaerobic degradation of 4-methylbenzoate by a new denitrifying bacterium, strain pMbN1.
Appl. Environ. Microbiol.,
DOI: 10.1128/AEM.06552-11
  Lüddeke F and Harder J (2011)
Enantiospecific (S)-(+)-linalool formation from β-myrcene by linalool dehydratase-isomerase.
Z. Naturforsch. 66c, 409−412
  Rabus R, Jarling R, Lahme S, Kühner S, Heider J, Widdel F and Wilkes H (2011)
Co-metabolic conversion of toluene in anaerobic n-alkane-degrading bacteria.
Environ. Microbiol. 13, 2576−2586
DOI: 10.1111/j.1462-2920.2011.02529.x
  Rotaru A-E, Schauer R, Probian C, Mußmann M and Harder J (2011)
Visualization of candidate division OP3 cocci in limonene degrading methanogenic cultures.
J. Microbiol. Biotechnol. 22, 457–461
DOI: 10.4014/jmb.1110.10055
  Steinbach A K, Fraas S, Harder J, Tabbert A, Brinkmann H, Meyer A, Ermler U and Kroneck P M H (2011)
Cyclohexane-1,2-dione hydrolase from denitrifying Azoarcus sp. strain 22Lin, a novel member of the thiamine diphosphate enzyme family.
J. Bacteriology 193, 6760-6769
DOI: 10.1128/JB.05348-11
  Zech H, Echtermeyer C, Wöhlbrand L, Blasius B and Rabus R (2011)
Biological versus technical variability in 2D DIGE experiments with environmental bacteria.
Proteomics 11, 3380−3389
DOI: 10.1002/pmic.201100071
2010 Amann J, Lange D, Schüler M and Rabus R (2010)
Substrate-dependent regulation of carbon catabolism in marine sulfate-reducing Desulfobacterium autotrophicum HRM2.
J Mol Microbiol Biotechnol 18:74–84
DOI: 10.1159/000277655
  Brodkorb D, Gottschall M, Marmulla R, Lüddeke F and Harder J (2010)
Linalool dehydratase-isomerase, a bifunctional enzyme in the anaerobic degradation of monoterpenes.
J. Biol. Chem. 285, 30436−30442
DOI: 10.1074/jbc.M109.084244
  Harder J (2010)
Anaerobic degradation of isoprene-derived compounds.
In: Handbook of hydrocarbon and lipid microbiology. Timmis, K.N. (ed.), Springer, Heidelberg.
DOI: 10.1007/978-3-540-77587-4_68
  Harder J (2010)
Isoprene, isoprenoids and sterols.
In: Handbook of hydrocarbon and lipid microbiology. Timmis, K.N. (ed.), Springer, Heidelberg.
DOI: 10.1007/978-3-540-77587-4_7
  Musat F, Wilkes H, Behrends A, Woebken D and Widdel F (2010)
Microbial nitrate-dependent cyclohexane degradation coupled with anaerobic ammonium oxidation.
ISME J. 4, 1290–1301
DOI: 10.1038/ismej.2010.50
  Neumann J, Grundmann O, Thöming J, Schulte S and Stolte S (2010)
Anaerobic biodegradability of ionic liquid cations under denitrifying conditions.
Green Chem. 12, 620-627
DOI: 10.1039/B918453H
  Rabus R and Trautwein K (2010)
Proteogenomics to study the anaerobic degradation of aromatic compounds and hydrocarbons.
In: Handbook of hydrocarbon and lipid microbiology. Timmis, K.N. (ed.), Springer, Heidelberg
DOI: 10.1007/978-3-540-77587-4_344
  Rotaru A-E, Probian C, Wilkes H and Harder J (2010)
Highly enriched Betaproteobacteria growing anaerobically with p-xylene and nitrate.
FEMS Microbiol. Ecol. 71:460-468
DOI: 10.1111/j.1574-6941.2009.00814.x
  Schauer R, Bienhold C, Ramette A and Harder J (2010)
Bacterial diversity and biogeography in deep-sea surface sediments of the South Atlantic Ocean.
ISME J. 4:159-170
DOI: 10.1038/ismej.2009.106
  Widdel F and Musat F (2010)
Energetic and other quantitative aspects of microbial hydrocarbon utilization.
In: Handbook of hydrocarbon and lipid microbiology. Timmis, K.N. (ed.), Springer, Heidelberg
DOI: 10.1007/978-3-540-77587-4_57
  Widdel F and Grundmann O (2010)
Biochemistry of the anaerobic degradation of non-methane alkanes.
In: Handbook of hydrocarbon and lipid microbiology. Timmis, K.N. (ed.), Springer, Heidelberg
DOI: 10.1007/978-3-540-77587-4_64
  Widdel F and Musat F (2010)
Diversity and common principles in enzymatic activation of hydrocarbons.
In: Handbook of hydrocarbon and lipid microbiology. Timmis, K.N. (ed.), Springer, Heidelberg
DOI: 10.1007/978-3-540-77587-4_70
  Widdel F, Knittel K and Galushko A (2010)
Anaerobic hydrocarbon-degrading microorganisms: an overview.
In: Handbook of hydrocarbon and lipid microbiology. Timmis, K.N. (ed.), Springer, Heidelberg
DOI: 10.1007/978-3-540-77587-4_146
  Widdel F (2010)
Cultivation of anaerobic microorganisms with hydrocarbons as growth substrates.
In: Handbook of hydrocarbon and lipid microbiology. Timmis, K.N. (ed.), Springer, Heidelberg
DOI: 10.1007/978-3-540-77587-4_298
  Winkelmann N, Jaekel U, Meyer C, Serrano W, Rachel R, Rosselló-Mora R and Harder J (2010)
Determination of the Diversity of Rhodopirellula Isolates from European Seas by Multilocus Sequence Analysis.
Appl. Environ. Microbiol. 76: 776–785
DOI: 10.1128/AEM.01525-09
  Zedelius J, Rabus R, Grundmann O, Werner I, Brodkorb D, Schreiber F, Ehrenreich P, Behrends A, Wilkes H, Kube M, Reinhardt R and Widdel F (2010)
Alkane degradation under anoxic conditions by a nitrate-reducing bacterium with possible involvement of the electron acceptor in substrate activation.
Environ. Microbiol. Reports 3, 125−135
DOI: 10.1111/j.1758-2229.2010.00198.x
  Zink K and Rabus R (2010)
Stress-induced changes in phospholipids in betaproteobacterium Aromatoleum aromaticum strain EbN1 due to alkylbenzene growth substrates.
J. Mol. Microbiol. Biotechnol. 18:92–101
DOI: 10.1159/000287988

 

2009Carvallo, C., Hickey, S., Faivre, D. and Menguy, N. (2009)
Formation of magnetite in Magnetospirillum gryphiswaldense studied with FORC diagrams.
Earth Planets and Space 61(1):143-150
Fraas, S., A.K. Steinbach, A. Tabbert, J. Harder, U. Ermler, K. Tittmann, A. Meyer and P.M.H. Kroneck (2009)
Cyclohexane-1,2-dione hydrolase: A new tool to degrade alicyclic compounds.
J. Mol. Cat. B: Enzymatic 61:47-49
Heip, C., H. Hummel, P. van Avesaath, W. Appeltans, C. Arvanitidis, R. Aspden, M. Austen, F. Boero, T.J. Bouma, C. Boxshall, F. Buchholz, T. Crowe, A. Delaney, T. Deprez, C. Embow, J.P. Feral, J.M. Gasol, A. Gooday, J. Harder, A. Ianora, A. Kraberg, B. Mackenzie, H. Ojaveer, D. Paterson, H. Rumohr, D. Schiedek, A. Sokolowski, P. Somerfield, I. Sousa Pinto, M. Vincx, J.M. Weslawski, R. Nash (2009)
Marine biodiversity and ecosystem functioning. Róisín Nash (ed.), Printbase, Dublin, Ireland.
Marine Biodiversity and Ecosystem Functioning EU Network of Excellence, Sustainable development, global change and ecosystems, GOCE-CT-2003-505446, ISSN 2009-2539 (2009), 100pp.
Holler T., G. Wegener, K. Knittel, A. Boetius, B. Brunner, M.M.M. Kuypers and F. Widdel (2009)
Substantial 13C/12C and D/H fractionation during anaerobic oxidation of methane by marine consortia enriched in vitro.
Environmental Microbiology Reports 1(5):370-376
DOI: 10.1111/j.1758-2229.2009.00074.x
Lin, Y. S., Biddle, J. F., Lipp, J. S., Holler, T., Teske, A., Hinrichs, K. U. (2009)
Stable carbon isotope probing of intact polar lipids from benthic archaea in marine subsurface sediment.
Geochimica et Cosmochimica Acta, Goldschmidt Conference Abstracts 73 (13,Suppl. S): A767
Lopez, O., Zuddas, P., Faivre, D. (2009)
The influence of temperature and seawater composition on calcite crystal growth mechanisms and kinetics: Implications for Mg incorporation in calcite lattice.
Geochimica et Cosmochimica Acta 73(2):337-347
Musat, F., Galushko, A., Jacob, J., Widdel, F., Kube, M., Reinhardt, R., Wilkes, H., Schink, B., Rabus, R. (2009)
Anaerobic degradation of naphthalene and 2-methylnaphthalene by strains of marine sulfate-reducing bacteria.
Environmental Microbiology 11(1):209–219
DOI: 10.1111/j.1462-2920.2008.01756.x
Strittmatter A. W., H. Liesegang, R. Rabus, I. Decker, J. Amann, S. Andres, A. Henne, W. F. Fricke, R.Martinez-Arias, D. Bartels, A. Goesmann, L. Krause, A. Pühler, H.-P. Klenk, M. Richter, M. Schüler, F. O. Glöckner, A. Meyerdierks, G. Gottschalk and R. Amann (2009)
Genome sequence of Desulfobacterium autotrophicum HRM2, a marine sulfate reducer oxidizing organic carbon completely to carbon dioxide.
Environ. Microbiol. 11(5):1038-1055
DOI: 10.1111/j.1462-2920.2008.01825.x
Tamang, D.G., R. Rabus, R.D. Barabote and M.H. Saier, Jr. (2009)
Comprehensive analyses of transport proteins encoded within the genome of Aromatoleum aromaticum strain EbN1.
J. Membr. Biol. 229(2):53-90
DOI: 10.1007/s00232-009-9168-2
Wecker, P., C. Klockow, A. Ellrott, C. Quast, P. Langhammer, J. Harder, and F. O. Glöckner (2009)
Transcriptional response of the model planctomycete Rhodopirellula baltica SH1T to changing environmental conditions.
BMC Genomics 10:410
DOI: 10.1186/1471-2164-10-410
Wietz, M., Hall, M. R., Høj, L. (2009)
Effects of seawater ozonation on biofilm development in aquaculture tanks.
Systematic and Applied Microbiology 32:266–277
DOI: 10.1016/j.syapm.2009.04.001
Winkelmann, N. and J. Harder (2009)
An improved isolation method for attached-living Planctomycetes of the genus Rhodopirellula.
J. Microb. Meth. 77:276-284
DOI: 10.1016/j.mimet.2009.03.002
Wöhlbrand L. and Rabus R. (2009)
Development of a genetic system for the denitrifying bacterium Aromatoleum aromaticum strain EbN1.
J. Mol. Microbiol. Biotechnol. 17:41–52
DOI: 10.1159/000159194
Yan, S., B.M. Fuchs, S. Lenk, J. Harder, J. Wulf, N.-Z. Jiao and R. Amann (2009)
Biogeography and phylogeny of the NOR5/OM60 clade of Gammaproteobacteria.
Syst. Appl. Microbiol. 32:124-139
DOI: 10.1016/j.syapm.2008.12.001
Zech, H., S. Thole, K. Schreiber, D. Kalhöfer, S. Voget, T. Brinkhoff, M. Simon, D. Schomburg and R. Rabus (2009)
Growth phase-dependent global protein and metabolite profiles of Phaeobacter gallaeciensis strain DSM 17395, a member of the marine Roseobacter-clade.
Proteomics 9:3677-3697
DOI: 10.1002/pmic.200900120
2008Amann, R., W. Goebel, B. Reinhold-Hurek, B. Schink, and F. Widdel (eds.) (2008)
Life strategies of microorganisms in the environment and in host organisms.
Nova Acta Leopoldina NF 96: 356
Faivre D., N. Menguy, M. Pósfai and D. Schüler (2008)
Environmental parameters affect the physical properties of fast-growing magnetosomes.
American Mineraolgist 93:463-469
DOI: 10.2138/am.2008.2678
Grundmann O., Behrends A., Rabus R., Amann J., Halder T., Heider J., Widdel, F. (2008)
Genes encoding the candidate enzyme for anaerobic activation of n-alkanes in the denitrifying bacterium, strain HxN1.
Environ. Microbiol. 10(2):376-385
DOI: 10.1111/j.1462-2920.2007.01458.x
Hünken M., Harder J., Kirst G.O. (2008)
Epiphytic bacteria on the Antarctic ice diatom Amphiprora kufferathii Manguin cleave hydrogen peroxide produced during algal photosynthesis.
Plant Biol. 10:519-526
DOI: 10.1111/j.1438-8677.2008.00040.x
Kamp A., Røy H., Schulz-Vogt H.N. (2008)
Video-supported analysis of Beggiatoa filament growth, breakage, and movement.
Microb. Ecol. 56:484-491
DOI: 10.1007/s00248-008-9367-x
Krüger M., H. Wolters, M. Gehre, S.B. Joye and H.-H. Richnow (2008)
Tracing the slow growth of anaerobic methane-oxidizing communities by 15N-labelling techniques.
FEMS Microbiol. Ecol. 63:401-411
DOI: 10.1111/j.1574-6941.2007.00431.x
Kühn S.F.and Köhler-Rink S.(2008)
pH effect on the susceptibility to parasitoid infection in the marine diatom Coscinodiscus spp. (Bacillariophyceae).
Mar. Biol 154:109-116
DOI: 10.1007/s00227-008-0904-4
Liebner S., J. Harder and D. Wagner (2008)
Bacterial diversity and community structure in polygonal tundra soils from Samoylov Island, Lena Delta, Siberia.
International Microbiology 11:195–202
DOI: 10.2436/20.1501.01.60
Mayr S., C. Latkoczy, M. Krüger, D. Günther, S. Shima, R.K. Thauer, F. Widdel and B. Jaun (2008)
Structure of an F430 variant from Archaea associated with anaerobic oxidation of methane.
J. Am. Chem. Soc. 130:10758–10767
DOI: 10.1021/ja802929z
Musat F., Galushko A., Jacob J., Widde, F., Kube M., Reinhardt R., Wilkes H., Schink B., Rabus R. (2008)
Anaerobic degradation of naphthalene and 2 methylnaphthalene by strains of marine sulfate-reducing bacteria.
Environ. Microbiol. 11(1):209-219
DOI: 10.1111/j.1462-2920.2008.01756.x
Musat F., Widdel F. (2008)
Anaerobic degradation of benzene by a marine sulfate-reducing enrichment culture, and cell hybridization of the dominant phylotype.
Environ. Microbiol. 10(1):10-19
DOI: 10.1111/j.1462-2920.2007.01425.x
Scheffel A., Gärdes A., GrünbergK ., Wanner G. and D. Schüler (2008)
The major magnetosome proteins MamGFDC are not essential for magnetite biomineralization in Magnetospirillum gryphiswaldense but regulate the size of megnetosome crystals.
Journal of Bacteriology 190(1):377-386
DOI: 10.1128/​JB.01371-07
Trautwein K., Kühner S., Wöhlbrand L., Halder T., Kuchta K., Steinbüchel A., Rabus R. (2008)
Solvent stress response of the denitrifying bacterium Aromatoleum aromaticum strain EbN1.
Appl. Environ. Microbiol. 74(8):2267-2274
DOI: 10.1128/AEM.02381-07
Widdel F. (2008)
Erneuerbare Energieträger aus Mikroorganismen – Möglichkeiten und Grenzen.
In: Die Zukunft der Energie. Gruss, P., Schüth, F. (Hrsg.), C.H. Beck, München
Wöhlbrand L., Rabus R. (2008)
Development of a Genetic System for the Denitrifying Bacterium Aromatoleum aromaticum Strain EbN1.
J. Mol. Microbiol. Biotechnol.
DOI: 10.1159/000159194
Wöhlbrand L., Wilkes H., Halder T., Rabus R. (2008)
Anaerobic degradation of p-Ethylphenol by Aromatoleum aromaticum strain EbN1: pathway, regulation, and involved proteins.
J. Bacteriol. 190(16):5699-5709
DOI: 10.1128/JB.00409-08
2007Büttner, M., P. Weber, F. Schmidl, A. Steppke, V. Grosse, T. Müller, M. Röder, P. Görnert, C. Lang, D. Schüler, and P. Seidel (2007)
Temperature-dependent Néel relaxation (TMRX) measurements on magnetosomes.
J. Magnetism and Magnetic Materials
Coker, V. S., C. I. Pearce, C. Lang, G. van der Laan, R.A.D. Pattrick, N. D. Telling, D. Schüler, E. Arenholz and J. R. Lloyd (2007)
Cation site occupancy of biogenic magnetite compared to polygenic ferrite spinels determined by X-ray magnetic circular dichroism.
European Journal of Mineralogy 19:707-716
DOI: 10.1127/0935-1221/2007/0019-1758
Faivre D. (2007)
Biomimetic Formation of Magnetite Nanoparticles.
In: Handbook of Biomineralization (Vol. 2): Biomimetic and Bio-inspired Materials Chemistry. E. Bäuerlein and P. Behrens (eds.), Wiley-VCH, Weinheim
DOI: 10.1002/9783527619443.ch33
Faivre D. , Böttger L., Matzanke B.F., and Schüler D. (2007)
Intracellular Magnetite Biomineralization in Bacteria Proceeds by a Distinct Pathway Involving Membrane-Bound Ferritin and an Iron (II) Species.
Angewandte Chemie International Edition 46: 8495-8499 and Angewandte Chemie 119: 8647-8652
DOI: 10.1002/anie.200700927
Hartung, A., M.R. Lisy, K.-H. Herrmann, I. Hilger, D. Schüler, C. Lang, M. E. Bellemann, W. A. Kaiser, and J. R. Reichenbach (2007)
Labeling macrophages using bacterial magnetosomes and their characterization by magnetic resonance imaging.
J. Magnetism and Magnetic Materials 311: 454-459
DOI: 10.1016/j.jmmm.2006.10.1153
Heider J., and Rabus R. (2007)
Genomic insights in the anaerobic biodegradation of organic pollutants.
In: Microbial biodegradation: genomics and molecular biology, E. Diaz (ed), Horizon Scientific Press
Knaust, F., M. Kube, R. Reinhardt, R. Rabus (2007)
Analyses of the vrl gene cluster in Desulfococcus multivorans: homologous to the virulence associated locus of the ovine footrot pathogen Dichelobacter nodosus strain A198.
J. Mol. Microbiol. Biotechnol. 13:156-164
DOI: 10.1159/000103607
Kniemeyer, O., F. Musat, S.M. Sievert, K. Knittel, H. Wilkes, M. Blumenberg, W. Michaelis, A. Classen, C. Bolm, S.B. Joye, and F. Widdel (2007)
Anaerobic oxidation of short-chain hydrocarbons by marine sulphate-reducing bacteria.
Nature 449:898-901
DOI: 10.1038/nature06200
Lang C., Schüler D. and Faivre D. (2007)
Synthesis of Magnetite Nanoparticles for Bio- and Nanotechnology: Genetic Engineering and Biomimetics of Bacterial Magnetosomes.
Macromolecular Bioscience 7:144-151
DOI: 10.1002/mabi.200600235
Lisy, M. R., A. Hartung, C. Lang, D. Schüler, W. Richter, J. R. Reichenbach, W. A. Kaiser, and I. Hilger (2007)
Fluoresecent bacterial magnetic nanoparticles as bimodal contrast agents.
Investigative Radiology 42:235-241
DOI: 10.1097/01.rli.0000255832.44443.e7
Meyer, B., and J. Kuever (2007)
Phylogeny of the alpha and beta subunits of the dissimilatory adenosine-5’-phosphosulfate (APS) reductase from sulfate-reducing prokaryotes – origin and evolution of the dissimilatory sulfate-reduction pathway.
Microbiology 153:2026-2044
DOI: 10.1099/mic.0.2006/003152-0
Meyer, B., and J. Kuever (2007)
Molecular analysis of the distribution and phylogeny of dissimilatory adenosine-5′-phosphosulfate reductase-encoding genes (aprBA) among sulfur-oxidizing prokaryotes.
Microbiology 153: 3478-3498
DOI: 10.1099/mic.0.2007/008250-0
Meyer, B., Imhoff, J.F., and J. Kuever (2007)
Molecular analysis of the distribution and phylogeny of the soxB gene among sulfur-oxidizing bacteria-evolution of the sulfur-oxidation (Sox)-sulfur-oxidation enzyme system.
Environ. Microbiol. 9(12):2957-2978
DOI: 10.1111/j.1462-2920.2007.01407.x
Meyer, B., and J. Kuever (2007)
Molecular analysis of the diversity of sulfate-reducing and sulfur-oxidizing prokaryotes in the environment, using aprA as functional marker gene.
Appl. Environ. Microbiol. 73(23):7664-7679
DOI: 10.1128/​AEM.01272-07
Meyer, B., and J. Kuever (2007)
Phylogenetic diversity and spatial distribution of the microbial community associated with the Caribbean deep-water sponge Polymastia cf. corticata by 16S rRNA, aprA and amoA gene analysis.
Microbial Ecology 56, 306-321,
DOI: 10.1007/s00248-007-9348-5
Nauhaus, K., M. Albrecht, M. Elvert, A. Boetius, and F. Widdel (2007)
In vitro cell growth of marine archaeal-bacterial consortia during anaerobic oxidation of methane with sulfate.
Environ. Microbiol. 9(1):187-196
DOI: 10.1111/j.1462-2920.2006.01127.x
Rabus R, and A. Strittmatter (2007)
Functional genomics of sulfate-reducing prokaryotes.
In: Sulphate-reducing bacteria - environmental and engineered systems. L.L. Barton and W.A. Hamilton (ed.), Cambridge University Press, Cambridge
DOI: 10.1017/CBO9780511541490.004
Richter, M., M. Kube, D. A. Bazylinski, T. Lombardot, F. O. Glöckner, R. Reinhardt, and D. Schüler (2007)
Comparative genome analysis of four magnetotactic bacteria reveals a complex set of group-specific genes implicated in magnetosome biomineralization and function.
J. Bacteriol. 189(13): 4899-4910
DOI: 10.1128/​JB.00119-07
Scheffel, A., and D. Schüler (2007)
The acidic repetitive domain of the Magnetospirillum gryphiswaldense MamJ protein displays hypervariability but is not required for magnetosome chain assembly.
J. Bacteriol. 189(17):6437-6446
DOI: 10.1128/​JB.00421-07
Wacker, R., B. Ceyhan, P. Alhorn, D. Schüler, C. Lang, and C.M. Niemeyer (2007)
Magneto immuno-PCR: A novel Immunoassay based on biogenic magnetosome nanoparticles.
Biochem. Biophys. Res. Commun. 357:391-396
DOI: 10.1016/j.bbrc.2007.03.156
Widdel, F., F. Musat, K. Knittel, and A. Galushko (2007)
Anaerobic degradation of hydrocarbons with sulphate as electron acceptor.
In: Sulphate-reducing bacteria - environmental and engineered systems. L.L. Barton and W.A. Hamilton (ed.), Cambridge University Press, Cambridge
DOI: 10.1017/CBO9780511541490.010
Wöhlbrand L, B. Kallerhoff, D. Lange, P. Hufnagel, J. Thiermann, R. Reinhardt, and R. Rabus (2007)
Functional proteomic view of metabolic regulation in Aromatoleum aromaticum strain EbN1.
Proteomics 7 2222-2239
DOI: 10.1002/pmic.200600987
2006Amann, R., J. Peplies, D. Schüler (2006)
Diversity and Taxonomy of Magnetotactic Bacteria.
In: Magnetoreception and Magnetosomes in Bacteria. D. Schüler(ed.), Springer Verlag Berlin Heidelberg
DOI: 10.1007/7171_037
Blumenberg M., Krüger M., Nauhaus K., Talbott H. M., Oppermann B. I., Seifert R., Pape T. and Michaelis W. (2006)
Biosynthesis of hopanoids by sulfate-reducing bacteria (genus Desulfovibrio).
Environmental Microbiology,
DOI: 10.1111/j.1462-2920.2006.01014.x
Ceyhan B, Alhorn P, Lang C, Schüler D, Niemeyer CM. (2006)
Semisynthetic biogenic magnetosome nanoparticles for the detection of proteins and nucleic acids.
Small 2(11): 1251-1255
DOI: 10.1002/smll.200600282
Dalisay D.S., Webb J.S., Scheffel A. Svenson C., James S., Holmström C., Egan S. and Kjelleberg S. (2006)
A mannose-sensitive haemagglutinin (MSHA)-like pilus promotes attachment of Pseudoalteromonas tunicata cells to the surface of the green alga Ulva australis.
Microbiology 152:2875-2883
DOI: 10.1099/mic.0.29158-0
Faivre D. and Zuddas P. (2006)
Mineralogical and isotopic properties of biogenic nanocrystalline magnetites.
In: Microbiology Monographs (Vol. 3), Magnetoreception and Magnetosomes in Bacteria, D. Schüler (ed.), Springer, Berlin, Heidelberg
DOI: 10.1007/7171_043
Grabovich M., Gavrish E., Kuever J., Lysenko A.M., Podkopaeva D.and Dubinina G. (2006)
Proposal of Giesbergeria voronezhensis gen. nov., sp. nov. and G. kuznetsovii sp. nov. and reclassification of (Aquaspirillum) anulus, (A.) sinuosum and (A.) giesbergeri as Giesbergeria anulus comb.nov., G.sinuosa comb. nov. and G. giesbergeri com. nov., and (Aquaspirillum) metamorphum and (A.) psychrophilum as Simplicispira metamorpha gen. nov., nov. and S. psychrophila comb. nov.
International Journal of Systematic and Evolutionary Microbiology 56:569-576
DOI: 10.1099/ijs.0.64027-0
Hirt A.M., Brem F., Hanzlik M., and Faivre D. (2006)
Anomalous magnetic properties of brain tissue at low temperature: The 50 K anomaly.
Journal of Geophyical Research 111:B12S06,
DOI: 10.1029/2006JB004570
Höffken H.W., Duong M., Friedrich T., Breuer M., Hauer B., Reinhardt R., Rabus R., Heider J. (2006)
Crystal structure and enzyme kinetics of the (S)-specific 1-phenylethanol dehydrogenase of the denitrifying bacterium strain EbN1.
Biochemistry 45: 82-93
DOI: 10.1021/bi051596b
Hufnagel P., Rabus R. (2006)
Mass spectrometric identification of proteins in complex post-genomic projects. Soluble proteins of the metabolically versatile, denitrifying Aromatoleum sp. strain EbN1.
Journal of Molecular Microbiology and Biotechnology 11:53-81
DOI: 10.1159/000092819
Ianora A., Boersma M., Casotti R., Fontana A., Harder J., Hoffman F., Pavia H., Potin P., Poulet S.A., Toth G. (2006)
New trends in marine chemical ecology.
Estuaries and Coasts 29:531-551
Jogler C., D. Schüler (2006)
Genetic Analysis of Magnetosome Biomineralization.
In: Magnetoreception and Magnetosomes in Bacteria. D. Schüler: (ed.), Springer Verlag Berlin, Heidelberg
DOI: 10.1007/7171_041
Lang, C., and D. Schüler (2006)
Biogenic nanoparticles: production, characterization, and application of bacterial magnetosomes.
Journal of Physics: Condensed Matter 18:S2815-S2828
DOI: 10.1088/0953-8984/18/38/S19
Lang C., Schüler, D. (2006)
Biomineralization of magnetosomes in bacteria: Nanoparticles with potential applications.
In: Microbial bionanotechnology: Biological self-assembly systems and biopolymer-based nanostructures. Rehm B (ed.), Horizon biosciences, Wymondham
Musat F, Harder J, Widdel F (2006)
Study of nitrogen fixation in microbial communities of oil-contaminated marine sediment microcosms.
Environmental Microbiology 8(10):1834-1843
DOI: 10.1111/j.1462-2920.2006.01069.x
Pósfai M., Moskowitz B.M., Arató B., Schüler D., Flies C., Bazylinski D.A., Frankel R.B. (2006)
Properties of intracellular magnetite crystals produced by Desulfovibrio magneticus strain RS-1.
Earth and Planetary Science Letters 249:444-455
DOI: 10.1016/j.epsl.2006.06.036
Rabus, R., T. Hansen and F. Widdel (2006)
Dissimilatory sulfate- and sulfur-reducing prokaryotes.
In: The prokaryotes, electronic edition. pp. 659-768, M. Dworkin, S. Falkow, E. Rosenberg, K.-H. Schleifer, E. Stackebrandt (eds.), Springer, New York
DOI: 10.1007/0-387-30742-7_22
Scheffel A., Gruska M., Faivre D., Linaroudis A., Plitzko J.M., Schüler D. (2006)
An acidic protein aligns magnetosomes along a filamentous structure in magnetotactic bacteria.
Nature 440:110-114
DOI: 10.1038/nature04382
Scheffel, A., and D. Schüler (2006)
Magnetosomes of magnetotactic bacteria.
In: Complex Intrecellular Structures in Prokaryotes. Vol. 1, J. M. Shively (ed.), Springer, Heidelberg
DOI: 10.1007/7171_024
Schübbe S., Würdemann C., Peplies J., Heyen U., Wawer C., Glöckner F.O., Schüler D. (2006)
Transcriptional organization and regulation of magnetosome operons in Magnetospirillum gryphiswaldense.
Applied and Environmental Microbiology 72(9):5757-5765
DOI: 10.1128/​AEM.00201-06
Seifert R., Nauhaus K., Blumenberg M., Krüger M., Michaelis W. (2006)
Methane dynamics in a microbial community of the Black Sea traced by stable carbon isotopes in vitro.
Organic Geochemistry 37:1411-1419
DOI: 10.1016/j.orggeochem.2006.03.007
Würdemann C., Peplies J., Schübbe S., Ellrott A., Schüler D., Glöckner F.O. (2006)
Evaluation of gene expression analysis using RNA-targeted partial genome arrays.
Systematic and Applied Microbiology 29:349-357
DOI: 10.1016/j.syapm.2006.03.005
2005Albrecht M., V. Janke, S. Sievers, U. Siegner, D. Schüler, and U. Heyen (2005)
Scanning force microscopy study of biogenic nanoparticles for medical applications.
J. Magnetism Magnetic Materials 290-291:269-271
DOI: 10.1016/j.jmmm.2004.11.206
Arató, B., Z. Szányi, C. Flies, D. Schüler, R. B. Frankel, P. R. Buseck, and M. Pósfai (2005)
Crystal-size and shape distributions of magnetite from uncultured magnetotactic bacteria as a potential biomarker.
American Mineralogist 90:1233-1241
DOI: 10.2138/am.2005.1778
Brinkhoff T., Kuever J., Muyzer G. and H.W. Jannasch (2005)
Genus VI. Thiomicrospira Kuenen and Veldkamp 1927, 253AL .
In: Bergey's Manual of Determinative Bacteriology. 2nd ed., Vol. II, Part B, D.J. Brenner, N.R. Krieg, J.T. Staley, G.M. Garrity (eds.), Springer, NY, USA
Eller G., P. Deines, J. Grey, H.-H. Richnow and M. Krüger (2005)
Methane cycling in lake sediments and its influence on chironomid larvae δ13C.
FEMS Microbiology Ecology 54:339-350
DOI: 10.1016/j.femsec.2005.04.006
Eberbeck, D., V. Janke, S. Hartwig, U. Heyen, D. Schüler, M. Albrecht, and L. Trahms (2005)
Blocking of magnetic moments of magnetosomes measured by magnetorelaxometry and direct observation by magnetic force microscopy.
J. Magnetism Magnetic Materials 289:70-73
DOI: 10.1016/j.jmmm.2004.11.020
Flies, C.B., J. Peplies and D. Schüler (2005)
Combined approach for characterization of uncultivated magnetotactic bacteria from various aquatic environments.
Applied and Environmental Microbiology 71(5):2723-2731
DOI: 10.1128/​AEM.71.5.2723-2731.2005
Flies, C., H.M. Jonkers, D. deBeer, K. Bosselmann, M.E. Böttcher, and D. Schüler (2005)
Diversity and vertical distribution of magnetotactic bacteria along chemical gradients in freshwater microcosms.
FEMS Microbiol. Ecol. 52:185-195
DOI: 10.1016/j.femsec.2004.11.006
Gade, D., J. Gobom and R. Rabus (2005)
Proteomic analysis of carbohydrate catabolism and regulation in the marine bacterium Rhodopirellula baltica.
Proteomics 5:3672-3683
DOI: 10.1002/pmic.200401200
Gade, D., Stührmann, T., Reinhardt, R. and R. Rabus (2005)
Growth phase dependent regulation of protein composition in Rhodopirellula baltica.
Envionmental Microbiology 7(8):1074-1084
DOI: 10.1111/j.1462-2920.2005.00784.x
Gade, D., D. Theiss, D. Lange, E. Mirgorodskaya, T. Lombardot, F.O. Glöckner, M. Kube, R. Reinhardt, R. Amann, H. Lehrach, R. Rabus and J. Gobom (2005)
Towards the proteome of the marine bacterium Rhodopirellula baltica: mapping the soluble proteins.
Proteomics 5:3654-3671
DOI: 10.1002/pmic.200401201
Hergt, R., R. Hiergeist, M. Zeisberger, D. Schüler, U. Heyen, I. Hilger, and W. A. Kaiser (2005)
Magnetic properties of bacterial magnetosomes as potential diagnostic and therapeutic tools.
J. Magnetism Magnetic Materials 293:80-86
DOI: 10.1016/j.jmmm.2005.01.047
Koch, B.P., J. Harder, R. J. Lara and G.Kattner (2005)
The effect of selective microbial degradation on the composition of mangrove derived pentacyclic triterpenols in surface sediments.
Organic Geochemistry 36:273-285
DOI: 10.1016/j.orggeochem.2004.07.019
Krüger M. and T. Treude (2005)
New insights into the physiology and regulation of the anaerobic oxidation of methane.
In: Microorganisms and earth systems - Advances in Geomicrobiology. Gadd, G. M., Semple, K. T. & Lappin-Scott, H. M. (eds.), SGM Microbiology 65, G. M. Gadd, K. T. Temple and H. M. Lappin-Scott (eds.), Cambridge University Press
DOI: 10.1017/CBO9780511754852.015
Krüger M., T. Treude, H. Wolters, K. Nauhaus and A. Boetius (2005)
Microbial methane turnover in different marine habitats.
Palaeogeography, Palaeoclimatology, Palaeoecology 227:6-17
DOI: 10.1016/j.palaeo.2005.04.031
Kube, M., A. Beck, A. Meyerdierks, R. Amann, R. Reinhardt and R. Rabus (2005)
A catabolic gene cluster for anaerobic benzoate degradation in methanotrophic microbial Black Sea mats.
Systematic and Applied Microbiology 28:287-294
DOI: 10.1016/j.syapm.2005.02.006
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Class IV. Deltaproteobacteria.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Order I. Desulfurellales.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Family I. Desulfurellaceae.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Order II. Desulfovibrionales.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Family I. Desulfovibrionaceae.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus I. Desulfovibrio.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Family II. Desulfomicrobiaceae.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Family III. Desulfohalobiaceae.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus III. Desulfothermus.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Family IV. Desulfonatronumaceae.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Order III. Desulfobacterales.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Family I. Desulfobacteraceae.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus I. Desulfobacter.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds),Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus II. Desulfobacterium.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus III. Desulfobacula.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus IV. Desulfobotulus.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus VI. Desulfococcus.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds),Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus VII. Desulfofaba.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus VIII. Desulfofrigus.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus IX. Desulfonema.
In:D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus X. Desulfosarcina.
In:D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus XII. Desulfotignum.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Family II. Desulfobulbaceae.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus I. Desulfobulbus.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus II. Desulfocapsa.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus IV. Desulforhopalus.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus V. Desulfotalea.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Order IV. Desulfarcales.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Family I. Desulfarculaceae.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus I. Desulfarculus.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Order V. Desulfuromonales.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Family I. Desulfuromonaceae.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus I. Desulfuromonas.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Order VI. Syntrophobacterales.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Family I. Syntrophobacteraceae.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus III. Desulforhabdus.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Genus IV. Desulfovirga.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Rainey, F.A., Widdel, F. (2005)
Family II. Syntrophaceae.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Schink, B. (2005)
Genus I. Syntrophus.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuever, J., Schink, B. (2005)
Genus III. Malonomonas.
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Kuehner, S., L. Wöhlbrand, I. Fritz, W. Wruck, C. Hultschig, P. Hufnagel, M. Kube, R. Reinhardt and R. Rabus (2005)
Substrate-dependent regulation of anaerobic degradation pathways for toluene and ethylbenzene in a denitrifying bacterium, strain EbN1.
Journal of Bacteriology 187(4):1493-1503
DOI: 10.1128/​JB.187.4.1493-1503.2005
Nauhaus K., T. Treude, A. Boetius and M. Krüger (2005)
Environmental regulation of the anaerobic oxidation of methane: A comparison of ANME-I or -II communities.
Environmental Microbiology 7(1):98-106
DOI: 10.1111/j.1462-2920.2004.00669.x
Rabus, R. (2005)
Biodegradation of hydrocarbons under anoxic conditions.
In: Petroleum Microbiology, Ollivier, B. and M. Magot (eds.), ASM Press, Washington, D.C.
Rabus, R. (2005)
Functional genomics of an anaerobic aromatic-degrading denitrifying bacterium, strain EbN1.
Applied Microbiology and Biotechnology 68:580-587
DOI: 10.1007/s00253-005-0030-x
Rabus, R., M. Kube, J. Heider, A. Beck, K. Heitmann, F. Widdel and R. Reinhardt (2005)
The genome sequence of an anaerobic aromatic-degrading denitrifying bacterium, strain EbN1.
Archives of Microbiology 183:27-36
DOI: 10.1007/s00203-004-0742-9
Schüler, D. (2005)
Nanokristalle für die Magnetfeldorientierung: Biomineralisation von Magnetosomen in Bakterien.
Biospektrum 3/11:291-294
Schüler, D., and K.H. Schleifer (2005)
Genus IV.The genus Magnetospirillum Schleifer
In: D.J. Brenner, N.R. Krieg, J.T. Staley and G. M. Garrity (eds), Bergey’s Manual of Systematic Bacteriology, second edition, Vol. 2 (The Proteobacteria), part C (The Alpha-, Beta-, Delta-, and Epsilonproteobacteria), Springer, New York
Schultheiss, D., R. Handrick, D. Jendrossek, M. Hanzlik and D. Schüler (2005)
The presumptive magnetosome protein Mms16 is a poly(3-hydroxybutyrate) granule-bound protein (phasin) in Magnetospirillum gryphiswaldense.
Journal of Bacteriology 187(7):2416-2425
DOI: 10.1128/​JB.187.7.2416-2425.2005
Ullrich, S., M. Kube, S. Schübbe, R. Reinhardt and D. Schüler (2005)
A hypervariable 130-kilobase genomic region of Magnetospirillum gryphiswaldense comprises a magnetosome island which undergoes frequent rearrangements during stationary growth.
Journal of Bacteriology 187(21):7176-7184
DOI: 10.1128/​JB.187.21.7176-7184.2005
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