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VAAM-Jahrestagung 2012 18.–21. März in Tübingen

VAAM-Jahrestagung 2012 18.–21. März in Tübingen

VAAM-Jahrestagung 2012 18.–21. März in Tübingen

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219showed reduced N 2O emissions <strong>in</strong> the biochar treatments up to 84%. Ingeneral N 2O emissions were 30 times higher under anoxic conditionscompared to the emissions from the oxic microcosms. Decreased N 2Oemissions were correlated to an <strong>in</strong>crease <strong>in</strong> the relative abundance of nitrousoxide reductase (nosZ) gene copy numbers dur<strong>in</strong>g the first two weeks afterbiochar addition. Our results further showed that reduced N 2O emissions frombiochar amended soils were directly l<strong>in</strong>ked to changes <strong>in</strong> the functionalcomposition, nitrogen compound utilization, and activity of the nitrogentransform<strong>in</strong>gmicrobial community. Overall, soil biochar amendment promotedcomplete denitrification via stimulation of growth and activity of nosZconta<strong>in</strong><strong>in</strong>g,nitrous oxide reduc<strong>in</strong>g denitrifiers. Our f<strong>in</strong>d<strong>in</strong>gs will facilitate thedevelopment of new mitigation strategies for anthropogenic GHGs.SMP023Microbial and metabolic analysis and optimization of CH 4production from wheat stillage at elevated temperaturesI. Röske* 1 , W. Sabra 2 , A. Sorger 1 , K. Sahm 1 , R. Daniel 3 , A.-P. Zeng 2 ,G. Antranikian 11 Hamburg University of Technology, Institute of Technical Microbiology,Hamburg, Germany2 Hamburg University of Technology, Institute for Bioprocess and BiosystemsEngeneer<strong>in</strong>g, Hamburg, Germany3 Georg-August-University, Department of Genomic and Applied Microbiology,Gött<strong>in</strong>gen, GermanyDevelopment of an efficient bioethanol production plant based on biomassrequires the <strong>in</strong>tegration of various biological and non-biological processes.After the bioconversion of wheat to ethanol and the distillation processhigh amounts of lignocellulose and dead yeast cells still rema<strong>in</strong> untreated(stillage). From a high-temperature biogas plant, us<strong>in</strong>g corn and chickenmanure as biogas substrates, a microbial community was enriched able toconvert wheat stillage to methane at 55°C.In order to <strong>in</strong>vestigate the microbial community <strong>in</strong> the model biogasreactor pyrosequence analysis of 16S rRNA gene-tags was conductedresult<strong>in</strong>g <strong>in</strong> 23,000 gene sequences. The studies <strong>in</strong>dicate the predom<strong>in</strong>anceof Archaea of the genera Methanosaeta and Methanothermobacter andBacteria of the families Thermotogaceae, Anaerol<strong>in</strong>eaceae,Synergistaceae and Thermodesulfobiaceae.The archaeon Methanothermobacter thermautotrophicus and the bacteriaLutispora thermophila, Thermoanaerobacter thermosaccharolyticum,Clostridium succ<strong>in</strong>ogenes and Thermohydrogenium kirishiense wereisolated by anaerobic serial dilution techniquesTo improve biogas production we <strong>in</strong>vestigated different stra<strong>in</strong>s for theirbioaugmentation potential. We could demonstrate that the addition of apure culture of Caldicellulosiruptor saccharolyticus to the exist<strong>in</strong>g biogascommunity resulted <strong>in</strong> a considerable biogas <strong>in</strong>tensification rate with aconstant CO 2/CH 4 ratio.To <strong>in</strong>vestigate dynamics and stability of the microbial community dur<strong>in</strong>gprocess modifications such as <strong>in</strong>crease <strong>in</strong> load<strong>in</strong>g rate and addition ofaccumulat<strong>in</strong>g <strong>in</strong>termediates, denatur<strong>in</strong>g gradient gel electrophoresis andfluorescence <strong>in</strong>-situ hybridization was employed. The results revealed thepresence of a robust consortium of methanogenic Archaea.The set of primers developed <strong>in</strong> this study provides a tool for monitor<strong>in</strong>gmethanogenic communities from a wide range of biogas processes.SMP024Methanogenic communities and their response to Holoceneand Late Pleistocene climate changes <strong>in</strong> permafrostenvironmentsD. Wagner* 1 , J. Griess 1 , K. Mangelsdorf 21 Alfred Wegener Institute for Polar and Mar<strong>in</strong>e Research, Research UnitPotsdam, Potsdam, Germany2 Helmholtz Zentrum Potsdam Deutsches Geoforschungszentrum, Section 4.3,Potsdam, GermanyThe currently observed climate change due to global warm<strong>in</strong>g is expectedto have a strong impact, notably on Arctic permafrost environments. Thethaw<strong>in</strong>g of permafrost is suggested to be associated with a massive releaseof greenhouse gases, <strong>in</strong> particular methane. Thus, Arctic permafrostregions play a fundamental role with<strong>in</strong> the global carbon cycle and thefuture development of Earth’s climate. To understand how the system willrespond to climate changes it is not only important to <strong>in</strong>vestigate thecurrent status of carbon turnover but also how the system reacted toclimate changes <strong>in</strong> the past.This presentation therefore takes a journey through time from the recentactive layer of permafrost to Holocene and Late Pleistocene permafrostdeposits <strong>in</strong> the Siberian Arctic, to reconstruct the microbial driven methanedynamics. Generally, <strong>in</strong>-situ methane contents of the deposits reflect theTOC profile with depth underl<strong>in</strong><strong>in</strong>g the correlation of the distribution oforganic matter and methanogenesis. Significant amounts of methane couldalso be found <strong>in</strong> Late Pleistocene deposits of an age of 30 and 41 ka,respectively. Lipid biomarkers and amplifiable DNA were successfullyrecovered throughout the whole permafrost sequences with an age of up to42 ka. Analysis of the abundance and distribution of archaeol, an <strong>in</strong>dicatorfor fossil methanogenic communities, revealed a temperature response toclimate changes dur<strong>in</strong>g the Late Pleistocene and Holocene. Past warm<strong>in</strong>gtrends seem to cause an enhanc<strong>in</strong>g of methanogenic communities, whilecool<strong>in</strong>g trends conversely caused them to decrease. Furthermore,<strong>in</strong>dications for recently liv<strong>in</strong>g archaeal communities <strong>in</strong> frozen groundcould be found, us<strong>in</strong>g phospholipid ether lipids (PLEL) and 16S rRNAf<strong>in</strong>gerpr<strong>in</strong>ts as specific markers. The obta<strong>in</strong>ed data on present and pastmethanogenic communities suggest a response to future warm<strong>in</strong>g events aswas reconstructed from previous warmer periods.SMP025FISH <strong>in</strong> soil: applications for the <strong>in</strong> situ <strong>in</strong>vestigation ofmicroorganismsH. Schmidt*, T. EickhorstUniversity of Bremen, Soil Science, Bremen, GermanyFluorescence <strong>in</strong> situ hybridization (FISH) represents a powerful methodfor the phylogenetic identification, enumeration, and visualization ofs<strong>in</strong>gle microbial cells <strong>in</strong> soil. The applicability of this tool for studies <strong>in</strong>soil microbiology is exemplarily shown on the basis of several FISHapproaches which are used <strong>in</strong> our lab.For rout<strong>in</strong>e applications of FISH <strong>in</strong> soil, the amplification of fluorescentsignals (CARD) is necessary for a clear discrim<strong>in</strong>ation of target signalsfrom the <strong>in</strong>tense background <strong>in</strong>duced by organic matter, high contents ofclay, and plant tissue. CARD-FISH <strong>in</strong> soil provides quantitative data ofs<strong>in</strong>gle microbial cells, and thus gives <strong>in</strong>sight <strong>in</strong>to the composition ofmicrobial consortia associated with different microenvironments (e.g. bulksoil and rhizosphere).With CARD-FISH applied to roots, the enumeration of s<strong>in</strong>gle cells as wellas the analysis of the spatial distribution of these microbes on therhizoplane gives additional <strong>in</strong>formation for comprehensive studies <strong>in</strong> thesoil-root <strong>in</strong>terface. Especially on roots, sequential hybridizations withfluorochromes of different spectral characteristics have shown to be usefulfor the analysis of microorganisms on doma<strong>in</strong> specific or hierarchic levels.The comb<strong>in</strong>ation of FISH and micropedology (res<strong>in</strong> embedd<strong>in</strong>g and th<strong>in</strong>section<strong>in</strong>g of soil samples) allows for the <strong>in</strong> situ detection of s<strong>in</strong>glemicroorganisms <strong>in</strong> the undisturbed soil matrix. The simultaneous use ofmultiple oligonucleotide probes thereby provides <strong>in</strong>formation on thespatial distribution of microorganisms belong<strong>in</strong>g to different taxonomicdivisions.In the recently developed gold-FISH protocol, conjugates labelled withfluorochromes and nanogold particles allow the comb<strong>in</strong>ative approach ofanalyz<strong>in</strong>g microorganisms by epifluorescence and scann<strong>in</strong>g electronmicroscopy. It is therefore possible to identify and localize s<strong>in</strong>gle microbialcells <strong>in</strong> situ on an ultrastructural level. Furthermore, the biochemical conditions<strong>in</strong> the microbial habitat of gold-FISH detected cells can be characterized byelement mapp<strong>in</strong>g generated with energy dispersive X-ray spectroscopy.SMP026Bacterial communities change along a glacier forefieldtransect - A comb<strong>in</strong>ed approach of molecular f<strong>in</strong>gerpr<strong>in</strong>ts (T-RFLP) and environmental analysesF. Bajerski*, D. WagnerAlfred Wegener <strong>in</strong>stitute for polar and mar<strong>in</strong>e research, PeriglacialResearch, Potsdam, GermanyGlacier forefields are known to be a pioneer site for primary successionand <strong>in</strong>habit extreme climatic and environmental conditions. Retreat<strong>in</strong>gglaciers expose new terrestrial terra<strong>in</strong> that becomes accessible for soilformation and microbial colonisation. Pioneer microorganisms supportweather<strong>in</strong>g processes and the colonisation of more complex microbialcommunities or plants. Because <strong>in</strong>creas<strong>in</strong>g temperatures due to climatechange enhance glacial degradation, it is important to understand howbacterial communities react to chang<strong>in</strong>g environmental conditions. Acomb<strong>in</strong>ed approach of geochemical and microbiological exam<strong>in</strong>ations willbe used to describe the habitat characteristics and the complex system ofmicrobial communities <strong>in</strong> two glacier forefields on Larsemann Hills, EastAntarctica. Term<strong>in</strong>al Restriction Length Polymorphism Analyses showthat bacterial community structures vary significantly between glacierforefields of different development status. Although relatively low,enzyme activities <strong>in</strong>crease with an advanced forefield development anddecrease with <strong>in</strong>creas<strong>in</strong>g depth. The extreme habitat conditions becomeapparent with<strong>in</strong> the geochemical and geochemical properties. The studysite is characterised by very low nutrient and water availability and acoarse gra<strong>in</strong> size. Statistics reveal a connection between environmental andbiological data and the position of the sample <strong>in</strong> the glacier forefield.Altogether our results show a high abundance and variability ofmicroorganisms <strong>in</strong> the hardly developed habitat glacier forefield.BIOspektrum | Tagungsband <strong>2012</strong>

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