EMP049Identification and characterization of aerobicchloroethene degrading bacteriaS. Mungenast* 1 , T. Teutenberg 2 , T. Schwartz 2 , K.R. Schmidt 1 , A. Tiehm 11 Department of Environmental Biotechnology, Water Center Technology(TZW), <strong>Karlsruhe</strong>, Germany2 Department of Interface Microbiology, <strong>Karlsruhe</strong> Institute of Technology(KIT), <strong>Karlsruhe</strong>, GermanyThe extensive use of chloroethenes as solvents and synthetic feed stocksover decades made those compounds to a major source of groundwater andsoil contamination. The bioremediation of chlorinated ethenes such as vinylchloride (VC) in groundwater via oxidation by aerobic microorganisms is acost-effective alternative to physical and chemical approaches. Metabolicpathways that use the target pollutant as growth substrate are favourable forbioremediation processes, as compared to cometabolic degradation in thepresence of auxiliary substrates. Several mixed cultures and pure bacterialstrains that can use VC as sole carbon and energy source have beenpublished and examined in regard to application as bioremediation agent.Recently, metabolic cis-1,2-dichloroethene (cDCE) degradation has beenreported for a mixed culture enriched at TZW [1; 2]. Concentration andtemperature range as well as starvation capacity and effects of cocontaminatingchloroethenes were determined. In our current joint study,also molecular biological approaches are applied. Two aerobic metabolicallyVC-degrading isolates from two different sites in Germany were identifiedby sequence analysis at KIT. Hydrogenophaga taeniospiralis andMycobacterium tusciae were identified as VC-degrading bacteria. PCR-DGGE and 16S-DNA sequence analysis allowed the identification andcharacterization of the degrading organisms using the basic local alignmentsearch tool of the NCBI database. The design of PCR primers andfluorescence in-situ hybridisation (FISH) probes for bacteria involved in theprocess of aerobic degradation is part of this project.Funding by BMWi and AiF (grant no. 16224 N) is gratefully acknowledged.[1] Schmidt K.R. et al (2010): Aerobic biodegradation of cis-1,2-dichloroethene as sole carbon source:Stable carbon isotope fractionation and growth characteristics. Chemosphere 78:527-532.[2] Zhao H.-P. et al (2010): Inhibition of aerobic metabolic cis-1,2-di-chloroethene biodegradation byother chloroethenes. Water Research 44:2276-2282.EMP050Occurrence of acidophilic and halotolerant Fe(II)-oxidizing microorganisms in high saline mine tailingsfrom the Atacama desert, ChileH. Korehi* 1 , D. Kock 1 , B. Dold 2 , A. Schippers 11 Federal Institute for Geosciences and Natural Resources , Microbiology,Hannover, Germany2 Institute of Applied Economic Geology (GEA), Department ofMicrobiology, University of Concepcion, Concepcion, ChileA marine shore copper mine waste tailings deposit in arid climate atChañaral, Chile, was studied to understand the influence of high salinity onthe microbial community composition and biogeochemical processes in thisextreme environment. Samples were taken from the oxidized zones atseveral sites which had a paste pH in the range of 2-8. The microbialcommunity was quantitatively analyzed using different methods: 1) total cellnumbers by SYBR Green II direct counting, 2) quantitative real-time PCR,3) most probable number cultivation of acidophilic Fe(II)-oxidizers. Theresults showed that the composition of microbial communities and the cellnumbers of different microbial groups are highly variable at differentsampling sites. Depth profiles of cell numbers of the mine tailings depositshowed total cell numbers in the range of 10 4 - 10 8 cells g -1 tailings. Bacteriadominated over Archaea in the mine tailings. The acidophilic Fe(II)- and/orsulfur-oxidizing Acidithiobacillus spp. dominated over the acidophilicFe(II)-oxidizing Leptospirillum spp. among the Gram-negative Bacteria. Inparallel to the microbial community analyses, novel acidophilic halotolerantFe(II)-oxidizing microorganisms were enriched at salt concentrations of upto 1 M probable suitable for metal bioleaching using seawater. Growth of upto 10 7 cells/ml was observed in case of complete oxidation of ferrous iron inthe medium. The growth of these microorganisms and its ability to oxidizeferrous iron were depended on pH, temperature, initial concentration offerrous iron, and the inoculum. High ferric to ferrous ratios exhibited aninhibitory effect on bacterial growth.EMP051Metagenome approach of two microbial biofilms in abiogas systemA. Rademacher* 1 , M. Zakzewski 2 , A. Schlüter 2 , M. Klocke 11 Department of Biotechnology, Leibniz Institute for Argicultural TechnologyPotsdam-Bornim e.V., Potsdam, Germany2 Centrum für Biotechnologie (CeBiTec), University of Bielefeld, Bielefeld,GermanyBiogas production forms a substantial component amongst the renewableenergy technologies converting biomass to methane. In order to improvebiogas production, a profound knowledge about the involvedmicroorganisms is essential.We investigated two biofilms of a thermophilic (55°C) two-phase leach-bedsystem in laboratory scale using a metagenome approach. This biogassystem with two internal circulations of leachate consisted of a gastighthydrolysis reactor, an effluent storage reactor and a downstream anaerobicfilter reactor. The retention time of the rye silage and the winter barley straw(w/w 10/1) was 21 days. Afterwards, samples of the digestate of thehydrolysis reactor (cellulolytic biofilm) and from a tower packing of theanaerobic filter reactor (methanogenic biofilm) were taken. The extractedDNA was sequenced by means of 454-pyrosequencing technology in aGenome Sequencer FLX Titanium System resulting in altogether 552,268reads with a total of 218 mb sequence information. The average read lengthwas 395 bases. Efficient characterization based on reads was applied usingseveral software pipelines as RDP classifier or CARMA software fortaxonomical analyses and Pfam or COG classification for functionalanalyses.Up to 30% of the obtained reads could be assigned to taxonomic ranksindicating that many up to now unknown microorganisms are participatingin the formation of methane. However, Clostridia, Thermotogae and Bacilliare the most prevalent classes among the bacteria in the cellulolytic biofilmsample and therefore may play a key role in carbohydrate degradation. Pfamcharacterization of enzymes also revealed Clostridia and Bacilli as prevalentfor carbohydrate degradation supporting the previous findings. In contrast,pfam analysis of the methanogenic biofilm sample showed a high abundanceof methanogenic enzymes for Methanobacteriales, whereas taxonomicalanalyses revealed that Methanosarcinales is highly abundant. These resultssuggest that the biofilm-based methanogenesis is not only driven by thehydrogenothrophic, but also by the acetoclastic pathway.In conclusion, the two biofilms, sampled from one biogas reactor, revealedstrong differences in taxonomical and functional analysis caused presumablyby reactor compartmentation.EMP052Genetic and biochemical characterization of ahydrothermal vent enrichment with autotrophichydrogen oxidizersM. Hansen*, M. PernerDepartment of Microbiology and Biotechnology, University of Hamburg,Hamburg, GermanyAn enrichment culture for autotrophic hydrogen oxidizing microbes,inoculated with diffuse fluids from the hydrothermal vent system SistersPeak (5°S on the Mid-Atlantic Ridge) was investigated with respect to themicrobial community composition, as well as the genetic and biochemicalfeatures with regard to hydrogen oxidation and CO 2 fixation.According to phylogenetic analyses (16S rRNA genes) Alpha- andGammaproteobacteria were detected, whereby the majority of sequenceswas related to Thalassospira. In contrast, 16S rRNA sequences generatedfrom isolated RNA by RT-PCR were mostly assigned to Thiomicrospiracrunogena. Interestingly, the relative abundances of Alpha- andGammaproteobacteria were 10 % and 11 %, respectively, whereas nearly 80% of all DAPI-stained cells could not be assigned to any bacterial group,although common probes targeting different Proteobacteria were used.None of the identified species are known for their ability to oxidize H 2.The only NiFe uptake hydrogenase (responsible for energy yielding H 2oxidation) identified by a PCR based screening of a metagenomic libraryfrom the culture using different primer sets was most similar to therespective gene from T. crunogena, which up to now has not been cultivatedwith H 2 as electron donor. But the transcription of this gene could not beconfirmed by RT-PCR yet. Recent investigations hint at the presence of ahydrogenase from Alteromonas macleodii, which was not amplified duringthe screening. But this needs further investigations to be confirmed. Theuptake hydrogenase activity of membrane associated proteins wasspektrum | Tagungsband <strong>2011</strong>
designated to be 4 fold higher than the activity of soluble proteins. Theseactivities indicate the oxidation of H 2 in the enrichment culture, but thespecies expressing hydrogenases could not yet be identified.Amplified sequences indicating CO 2 fixation via the Calvin Cycle matchedthe respective gene of T. crunogena.Additionally, to confirm and amend these first results, future investigationsshall include the identification of the hydrogenase expressing species,determination of hydrogen consumption rates and purification of thehydrogenase.EMP053Will not be presented!EMP054Bacterial degradation of 1H-benzotriazoleB. Morasch*, V. Heesel, D. Ilieva, S. HaderleinCenter for Applied Geoscience, Eberhard Karls University, Tübingen,GermanyThe complexing agent 1H-benzotriazole (BT) is a widely-used corrosioninhibitor in cooling and heating fluids, dishwashing detergents, and aircraftde-icing fluids. Due to its apparent persistence against biodegradation, it isubiquitously present in the aquatic environment. This is even more alarmingsince the compound has toxic effects. So far, BT has been considered nonbiodegradableby bacteria under oxic and anoxic conditions.In this study, we investigated the presence of an intrinsic biodegradationpotential for BT in two environmentally relevant compartments: sewagesludge and deep aquifer sediments. An aerobic sewage-sludge-derivedmixed culture coupled BT degradation with bacterial growth. Duringbiodegradation of BT, N-methylaniline and further transformation productswith absorption maxima at 367 and 550 nm were formed. This is the firstreport on bacterial growth with BT at mesophilic temperatures andunderlines that sewage sludge is a habitat of microorganisms can potentiallydegrade BT. The anaerobic intrinsic biodegradation potential for BT wasstudied in deep aquifer sediments eventually contaminated by heat transferfluids leaking from borehole heat exchangers. Concentrations of BT and itsderivative methyl-benzotriazole stayed constant over a period of more than200 days indicating that no intrinsic biodegradation potential was detectableunder the various redox conditions investigated.EMP055Dynamic of microbial communities in anaerobic biogasreactorsK. Heeg* 1,2 , M. Sontag 1 , E. Nettmann 11 APECS Nachwuchsgruppe, Leibniz Institute for Agricultural TechnologyPotsdam-Bornim e.V., Potsdam, Germany2 Department of Environmental Technology, Chair EnvironmentalMicrobiology, Institute of Technology, Berlin, GermanyKnowledge about the composition and function of microbial communitiesresponsible for substrate degradation and formation of biogas in anaerobicdigestion reactors is still rather incomplete. In this study, the dynamic of themicrobial diversity from start-up to the development of a stable biogasformation process into anaerobic digesters was investigated. The anaerobicdigestion was performed into an up-flow leach-bed reactor combined with amethane reactor and recirculation of the liquid phase. Reactors werecontinuously fed with wheat straw and run at thermophilic (56°C) andmesophilic (36°C) conditions. Samples were taken from the liquid phase anddigestate. Additionally, at stable process conditions, carrier bodies from themethane reactor were sampled. Terminal-restriction-fragment polymorphism(T-RFLP) of restriction endonuclease digested PCR-amplified 16S rDNAwas applied to analyse changes into the community structures. Furthermore,16S rRNA gene libraries were constructed to get detailed insights into thecomposition of the microbial communities at the date of start-up phase andstable process of biogas formation. The results of this study provide a basisfor the modelling and optimisation of the overall anaerobic digestion processwithin the APECS project. The aim of APECS (Anaerobic Pathways torenewable Energies and Carbon Sinks) is to provide the scientific andtechnical basis for an efficient and sustainable production of bio-methane asa high quality fuel and biochar as a long lasting carbon sink and an efficientsoil improver.EMP056Comparative and functional genomics ofMethylobacterium and Hyphomicrobium strainsdegrading halogenated methanesE. Muller 1 , A. Lajus 2 , M. Farhan Ul Haque 1 , T. Nadalig 1 , C. Gruffaz 1 ,Y. Louhichi 1 , V. Barbe 2 , S. Mangenot 2 , C. Médigue 2 , F. Bringel 1 ,S. Vuilleumier* 21 University of Strasbourg, Strasbourg, France2 LABGeM, Genoscope-IG-CEA, Evry, FranceThe halogenated methanes dichloromethane and chloromethane are volatiletoxic halogenated solvents produced both naturally and industrially.Dichloromethane- and chloromethane-degrading bacteria have been modelsof choice to study microbial dehalogenation metabolism at thephysiological, biochemical and genetic levels. A comparative analysis ofcomplete genome sequences of halogenated methane degradingMethylobacterium and Hyphomicrobium strains (Vuilleumier et al., 2009;Muller et al., accepted), obtained at Genoscope and the US American JointGenomic Institute, was performed to complement the investigation ofdichloromethane- and chloromethane-degrading bacteria using functionalgenomics approaches (Muller et al., submitted; Roselli et al., submitted).Our study highlights both the importance of horizontal gene transfer in thedissemination of halomethane degradation genes in the environment, and theinvolvement of the Alphaproteobacterial core genome in specific adaptationsto dehalogenative metabolism.[1] Vuilleumier, S. et al (2009): Methylobacterium genome sequences: a reference blueprint toinvestigate microbial metabolism of C1 compounds from natural and industrial sources. PLoS ONE 4,e5584.[2] Muller, E. et al (accepted). Dichloromethane-degrading bacteria in the genomic age. Res.Microbiol.EMP057Metaproteomics to investigate the impact of sampling-sitebiogeochemistry on structure and functionality of leaflitterdegrading microbial communitiesT. Schneider 1 , K. Keiblinger 2 , M. Kucklick* 3 , E. Schmid 1 , L. Eberl 1 ,S. Zechmeister-Boltenstern 2 , K. Riedel 31 Institute of Plant Biology, University of Zürich, Zurich, Switzerland2 Federal Office and Research Center for Forests – BFW, Vienna, Austria3 Institute of Microbiology, University of Technology, Braunschweig,GermanyThe composition of organic matter in natural ecosystems is stronglyinfluenced by the microorganisms present. Conversely, bacteria and fungiare limited by the amount and type of organic matter available in a givenenvironment, most of which is ultimately derived from plants. Changes inthe stoichiometry and biochemical constituents of plant litter may thereforealter species composition and elicit changes in the activities of microbialcommunities and their component parts. The identification of the microbialproteins of a given habitat together with the analysis of their phylogeneticorigin and their spatial and temporal distribution are expected to providefundamentally new insights into the role of microbial diversity inbiogeochemical processes.To relate structure and functionality of microbial communities involved inleaf-litter decomposition we determined biogeochemistry, communitystructure (PFLA-analyses), enzymatic activities, and analysed the proteincomplement of different litter types, which were collected in winter andspring at various Austrian sampling sites, by a semi-quantitative proteomicsapproach (1-D-SDS-PAGE combined with LC-MS/MS). In samples withhigh manganese and phosphor content a significant increase of fungalproteins from February to May was observed, which was in good agreementwith the PFLA-analyses showing similar trends towards an increase of thefungal community. In contrast, the PFLA analysis revealed no temporalchanges in the community at Achenkirch and even a decrease in thefungal/bacterial ratio at Klausen-Leopoldsdorf, two sampling sites low in Pand Mn; similar trends are reflected in our spectral counts. In conclusion,semi-quantitative proteome- and PFLA-analyses suggest that fungal andbacterial abundance positively correlates with the total amount of P and Mnwithin the different litter types. Spectral counts of extracellular enzymesdemonstrated a significant increase of these enzymes in the May, which wasalso mirrored by measurements of total enzymatic activities. The findingthat almost all hydrolytic enzymes identified from litter were of fungalorigin suggests a prominent role of fungi during aerobic litterdecomposition.spektrum | Tagungsband <strong>2011</strong>
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3Vereinigung für Allgemeine und An
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8 GENERAL INFORMATIONGeneral Inform
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12 GENERAL INFORMATION · SPONSORS
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14 GENERAL INFORMATIONEinladung zur
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16 AUS DEN FACHGRUPPEN DER VAAMFach
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18 AUS DEN FACHGRUPPEN DER VAAMFach
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20 AUS DEN FACHGRUPPEN DER VAAMFach
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22 INSTITUTSPORTRAITMicrobiology in
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INSTITUTSPORTRAITGrundlagen der Mik
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26 CONFERENCE PROGRAMME | OVERVIEWT
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28 CONFERENCE PROGRAMMECONFERENCE P
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32 SPECIAL GROUPSACTIVITIES OF THE
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36 SHORT LECTURESMonday, April 4, 0
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42 SHORT LECTURESWednesday, April 6
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ISV01The final meters to the tapH.-
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ISV11No abstract submitted!ISV12Mon
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ISV22Applying ecological principles
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ISV31Fatty acid synthesis in fungal
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GWV012Autotrophic Production of Sta
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EPS matrix showed that it consists
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enzyme was purified via metal ion a
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finally aim at the inactivation of
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Results: 4 of 9 parent strains were
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GWP047Production of microbial biosu
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Based on these foregoing works we h
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function, activity, influence on gl
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selected phyllosphere bacteria was
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groups. Multiple isolates were avai
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Dinoroseobacter shibae for our knoc
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Here, we present a comparative prot
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MPV009Connecting cell cycle to path
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MPV018Functional characterisation o
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dependent polar flagellum. The torq
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(ciprofloxacin, gentamicin, sulfame
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that can confer cell wall attachmen
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hemagglutinates sheep erythrocytes.
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about 600 bacterial proteins from o
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NTP003Resolution of natural microbi
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an un-inoculated reference cell, pr
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NTP019Identification and metabolic
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OTV008Structural analysis of the po
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and at least 99.5% of their respect
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[2] Garcillan-Barcia, M. P. et al (
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OTP022c-type cytochromes from Geoba
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To characterize the gene involved i
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OTP037Identification of an acidic l
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PSP006Investigation of PEP-PTS homo
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The gene product of PA1242 (sprP) c
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PSP022Genome analysis and heterolog
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Correspondingly, P. aeruginosa muta
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RGP002Bistability in myo-inositol u
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a novel initiation mechanism operat
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RGP035Kinase-Phosphatase Switch of
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RGP043Influence of Temperature on e
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[3] was investigated. The specific
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transcriptionally induced in respon
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during development of the symbiotic
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Such a prodrug-activation mechanism
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cations. Besides the catalase depen
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Based on the recently solved 3D-str
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SRP016Effect of the sRNA repeat RSs
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CODH after overexpression in E. col
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acteriocines, proteins involved in
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264 AUTORENBreinig, F.FBP010FBP023B
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266 AUTORENGoerke, C.Goesmann, A.Go
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268 AUTORENKlaus, T.Klebanoff, S. J
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270 AUTORENMüller, Al.Müller, Ane
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272 AUTORENScherlach, K.Scheunemann
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274 AUTORENWagner, J.Wagner, N.Wahl
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276 PERSONALIA AUS DER MIKROBIOLOGI
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278 PROMOTIONEN 2010Lars Schreiber:
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280 PROMOTIONEN 2010Universität Je
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282 PROMOTIONEN 2010Universität Ro
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Die EINE, auf dieSie gewartet haben