52ISV01Die verborgene Welt der Bakterien und ihre Bedeutung fürdas Leben auf der ErdeK.-H. SchleiferTechnische Universität München, Mikrobiologie, München, GermanyBei Bakterien denken die meisten Menschen an Krankheitserreger. Dochdie überwiegende Mehrheit dieser Organismen ist harmlos oder sogarnützlich. Sie spielen e<strong>in</strong>e wichtige Rolle bei der Herstellung fermentierterLebensmittel oder <strong>in</strong> der weißen Biotechnologie. Die zellkernlosenProkaryoten (Bakterien + Archaeen) s<strong>in</strong>d jedoch noch aus anderenGründen sehr wichtig. Sie kommen <strong>in</strong> ungeheuer großen Zahlen vor undmachen ca. 50% der globalen Biomasse aus. Leider ist bisher nur e<strong>in</strong>Bruchteil von ihnen bekannt, da sie als Re<strong>in</strong>kultur nicht zugänglich s<strong>in</strong>d.Durch genotypische Methoden, <strong>in</strong>sbesondere durch vergleichendeSequenzanalyse der 16S-rRNS Gene ist es allerd<strong>in</strong>gs möglich, dieOrganismen auch ohne vorherige Kultivierung zu identifizieren. Mit Hilfemaßgeschneiderter, fluoreszenzmarkierter Oligonukleotidsonden, die ankomplementäre Sequenzen der 16S-rRNS b<strong>in</strong>den, lassen sich dieOrganismen auch <strong>in</strong> situ nachweisen und identifizieren. Dies soll anhandverschiedener Beispiele belegt werden.Die Prokaryoten s<strong>in</strong>d die Wegbereiter der Biosphäre. Für m<strong>in</strong>destens 2Milliarden Jahre waren sie die e<strong>in</strong>zigen Lebewesen auf unserem Planeten.Sie waren an der Entstehung der höheren Lebewesen (Eukaryoten)beteiligt, und die Cyanobakterien sorgten für den nötigen Sauerstoff aufder Erde. Der Nährstoffkreislauf, <strong>in</strong>sbesondere Stickstoff-und Schwefelkreislauf,wäre ohne die Prokaryoten unvollständig. Überdies zeichnen siesich durch e<strong>in</strong>zigartige Mechanismen der Energiegew<strong>in</strong>nung aus, und siesetzen auch die Grenzen des Lebens fest. Sie wachsen überall, wo nochflüssiges Wassers vorkommt.Die Bakterien spielen auch e<strong>in</strong>e besondere Rolle <strong>in</strong> der Evolution undÖkologie der Eukaryoten. Sie können als Kommensalen, Endo- oderEktosymbionten vorkommen. Dies soll an verschiedenen Beispielengezeigt werden.Bakterien und Archaeen s<strong>in</strong>d durch ihre vielfältigen Aktivitäten wichtigfür Umwelt und Klima. Sie s<strong>in</strong>d entscheidend an Aufbau und Erhalt derBiosphäre beteiligt. Ohne sie wäre die M<strong>in</strong>eralisierung organischer Stoffeunvollständig und ohne sie gäbe es auch nicht die typischen Eukaryoten.Der Vorläufer der heutigen Mitochondrien, den Energiekraftwerken dereukaryotischen Zellen, gehört zu den Alpha-Proteobakterien und dieChloroplasten, <strong>in</strong> denen die Photosynthese stattf<strong>in</strong>det, stammen vonCyanobakterien ab. All dies spricht dafür, dass es ohne Bakterien ke<strong>in</strong>Leben auf unserem Planeten gäbe.ISV02From microorganisms to the atmosphere: flooded soils and themethane cycleR. ConradMax-Planck-Institut für terrestrische Mikrobiologie, Biogeochemie,Marburg, GermanyFlooded soils such as rice fields and wetlands are the most importantsource for the greenhouse gas methane. Rice fields, <strong>in</strong> particular, serve asmodel for study<strong>in</strong>g the role of the structure of anaerobic microbialcommunities for ecosystem function<strong>in</strong>g and the partition<strong>in</strong>g of carbon fluxalong different paths of degradation of organic matter to methane. Floodedsoils are relatively rapidly depleted of oxygen and other oxidants such asferric iron and sulfate. Then, organic matter degradation results <strong>in</strong> theproduction methane. Methane is eventually produced from different typesof organic matter, ma<strong>in</strong>ly from plant litter, root exudates, and soil organicmatter. Methane production is achieved by a community consist<strong>in</strong>g ofhydrolytic, ferment<strong>in</strong>g and methanogenic microorganisms. Acetate andhydrogen (plus CO 2) are the two most important fermentation productsthat are used as methanogenic substrates to different extent. The transportof CH 4 to the atmosphere is ma<strong>in</strong>ly partitioned between transport throughthe aerenchyma system of plants, gas ebullition and diffusion. Transportthrough oxygenated zones such as the surface soil or the rhizosphereresults <strong>in</strong> oxidation of a substantial percentage of methane bymethanotrophic bacteria thus attenuat<strong>in</strong>g the methane flux <strong>in</strong>to theatmosphere. Tracer experiments (e.g. us<strong>in</strong>g stable carbon isotopes) areuseful for quantify<strong>in</strong>g the partition<strong>in</strong>g of carbon flux along different pathsand for elucidat<strong>in</strong>g the active microbial groups <strong>in</strong>volved <strong>in</strong> carbontransformation.ISV03Physiology, mechanisms and habitats of microbial Fe(II) oxidationA. KapplerUniversity of Tüb<strong>in</strong>gen, Geomicrobiology, Center for AppliedGeosciences, Tüb<strong>in</strong>gen, GermanyThe two most important redox states of iron <strong>in</strong> the environment are Fe(II)[ferrous iron] and Fe(III) [ferric iron]. Dissolved Fe(II), relatively solubleFe(II) m<strong>in</strong>erals and poorly soluble Fe(III) m<strong>in</strong>erals are abundant <strong>in</strong> pHneutralsoils and sediments. Redox transformation of iron lead<strong>in</strong>g either todissolution, transformation or precipitation of iron m<strong>in</strong>erals is used bymany microorganisms to produce energy and to grow. Oxidation ofdissolved ferrous iron [Fe(II)] at neutral pH can be catalyzed byacidophilic aerobic and neutrophilic microaerophilic, nitrate-reduc<strong>in</strong>g andeven phototrophic microorganisms. This contribution will present thecurrent knowledge and new results regard<strong>in</strong>g mechanisms, physiology,ecology and environmental implications of microbial Fe(II) oxidation.Special focus will be on microaerophilic Fe(II)-oxidiz<strong>in</strong>g bacteria thatthrive <strong>in</strong> gradients of ferrous iron and oxygen (e.g. at the surface of riceroots <strong>in</strong> paddy soil), phototrophic Fe(II)-oxidiz<strong>in</strong>g autotrophs liv<strong>in</strong>g <strong>in</strong>surface near environments such as littoral sediments, and f<strong>in</strong>ally on nitratereduc<strong>in</strong>gbacteria oxidiz<strong>in</strong>g Fe(II) <strong>in</strong> soils and sediments.ISV04Assembly and function of archaeal surface structuresS.-V. AlbersMax-Planck-Institut für terrestrische Mikrobiologie, Marburg, GermanyArchaea, the third doma<strong>in</strong> of life, possess a variety of surface structuressuch as pili and flagella. These structures have <strong>in</strong> common that they arecomposed of subunits that are found <strong>in</strong> bacterial type IV pili which amongothers are <strong>in</strong>volved <strong>in</strong> bacterial pathogenesis. The archaeal pili and flagellasystems appear to be much simpler than their bacterial counterparts and aretherefore well suited model systems to understand the mechanistic of theassembly process.The thermoacidophilic archaeon Sulfolobus acidocaldariusexhibits three different surface appendages, (i) flagella, (ii) th<strong>in</strong> pili, and (iii) UVlight <strong>in</strong>duced pili. In Sulfolobus the flagellum is ma<strong>in</strong>ly <strong>in</strong>volved <strong>in</strong> adhesion andsurface motility, which seems to be <strong>in</strong>hibited by the th<strong>in</strong> pili. The UV <strong>in</strong>ducedpili <strong>in</strong>itiate cell aggregation after DNA damage and subsequent DNA repair byconjugation. Next to the physiological function of these surface structures ourunderstand<strong>in</strong>g of their assembly will be discussed.ISV05Current views on the role as well as the fate of host cellsdur<strong>in</strong>g <strong>in</strong>fectionThomas F. Meyer and coworkersDepartment of Molecular Biology, Max Planck Institute for Infection Biology,Berl<strong>in</strong>, GermanyInfectious disease research has led us to the realization that the <strong>in</strong>itiationand progression of <strong>in</strong>fection are critically dependent on both pathogen andhost determ<strong>in</strong>ants. Microbial virulence factors have been studied <strong>in</strong> greatdetail over the past decades; however, the role of host determ<strong>in</strong>ants as thecounterparts of pathogen virulence factors and signal transductionelements has been less <strong>in</strong>tensely pursued. With the discovery of RNAi, anextremely useful tool has become available that facilitates the assessmentof host-cell determ<strong>in</strong>ants and their role <strong>in</strong> <strong>in</strong>fection at the genome-widelevel. Here, I present two examples of global host-cell function analysis,address<strong>in</strong>g <strong>in</strong>fluenza virus and Chlamydia <strong>in</strong>fections (1,2), and discuss theimplications for the development of a novel class of therapeutic drugs aswell as for our future understand<strong>in</strong>g of host susceptibility to <strong>in</strong>fection andmorbidity/mortality determ<strong>in</strong>ants.Host cells are not merely vehicles for pathogen replication; it appears hostcells are also subject to genetic and epigenetic modifications dur<strong>in</strong>g<strong>in</strong>fection, and are therefore capable of acquir<strong>in</strong>g heritable features that mayunderlie pathological sequelae, <strong>in</strong>clud<strong>in</strong>g cancer. The gastric pathogenHelicobacter pylori is the paradigm of a cancer-<strong>in</strong>duc<strong>in</strong>g bacterium (3).We, and others, can show that H. pylori and other bacterial pathogens arecapable of caus<strong>in</strong>g genetic and epigenetic lesions <strong>in</strong> <strong>in</strong>fected cells (4).However, DNA damage alone does not seem to be sufficient <strong>in</strong> itself forcarc<strong>in</strong>ogenesis. Other features such as persistence of <strong>in</strong>fection andmitogenic stimuli are likely cofactors (5).1. Karlas, A., N.Machuy, Y.Sh<strong>in</strong>, K.-P.Pleissner, A.Artar<strong>in</strong>i, D.Heuer, D.Becker, H.Khalil, L.A.Ogilvie,S.Hess, A.P.Mäurer, E.Müller, T.Wolff, T.Rudel, and T.F.Meyer. 2010. Genome-wide RNAi screenidentifies human host factors crucial for <strong>in</strong>fluenza virus replication. Nature 463:818-822.2. Gurumurthy, R.K., A.P.Mäurer, N.Machuy, S.Hess, K.P.Pleissner, J.Schuchhardt, T.Rudel, andT.F.Meyer. 2010. A loss-of-function screen reveals Ras- and Raf-<strong>in</strong>dependent MEK-ERK signal<strong>in</strong>g dur<strong>in</strong>gChlamydia trachomatis <strong>in</strong>fection. Science Signal<strong>in</strong>g 3:ra21.3. Bauer, B., and T.F.Meyer. 2011. The human gastric pathogen Helicobacter pylori and its association withgastric cancer and ulcer disease. Ulcers. doi:10.1155/2011/3401574. Fassi Fehri, L., C.Rechner, S.Janssen, T.N.Mak, C.Holland, S.Bartfeld, H.Bruggemann, and T.F.Meyer.2009. Helicobacter pylori-<strong>in</strong>duced modification of the histone H3 phosphorylation status <strong>in</strong> gastric epithelialcells reflects its impact on cell cycle regulation. Epigenetics. 4:577-586.5. Kessler, M., J.Zielecki, O.Thieck, H.J.Mollenkopf, C.Fotopoulou, and T.F.Meyer. 2011. ChlamydiaTrachomatis Disturbs Epithelial Tissue Homeostasis <strong>in</strong> Fallopian Tubes via Paracr<strong>in</strong>e Wnt Signal<strong>in</strong>g. Am. JPathol..180:186-198.ISV06No abstract submitted!BIOspektrum | Tagungsband <strong>2012</strong>
53ISV07Teichoic acids <strong>in</strong> Gram-positive cell wall function and host<strong>in</strong>teractionA. PeschelUniversitätskl<strong>in</strong>ikum Tüb<strong>in</strong>gen, Medical Microbiology and HygieneDepartment, Tüb<strong>in</strong>gen, GermanyThe presence of teichoic acids or related polyanionic glycopolymers hasrema<strong>in</strong>ed an enigmatic trait of most Gram-positive bacterial cellenvelopes. Recent advances <strong>in</strong> teichoic acids biosynthesis and theavailability of def<strong>in</strong>ed mutants now permit to explore the roles of teichoicacids, which exhibit extensive species or stra<strong>in</strong>-specific differences <strong>in</strong>composition and glycosylation but share polyanionic properties. Althoughnot essential to bacterial viability recent studies <strong>in</strong>dicate that teichoic acidare crucial for direct<strong>in</strong>g cell envelope metabolism and turn-over and forgovern<strong>in</strong>g the capacity of host-adapted Gram-positive bacteria to colonizeand <strong>in</strong>fect mammalian host organisms. Therefore, teichoic acids representattractive targets for new antibacterial therapeutics aga<strong>in</strong>st staphylococciand other Gram-positive human pathogens.ISV08Out of the iron age: the battle for z<strong>in</strong>cJ. TommassenUtrecht University, Molecular Microbiology, Utrecht, NetherlandsThe cell envelope of Gram-negative bacteria consists of two membranes,which are separated by the periplasm conta<strong>in</strong><strong>in</strong>g the peptidoglycan layer.The outer membrane is an asymmetrical bilayer consist<strong>in</strong>g ofphospholipids <strong>in</strong> the <strong>in</strong>ner leaflet and lipopolysaccharides <strong>in</strong> the outerleaflet. It functions as a barrier for harmful compounds from theenvironment <strong>in</strong>clud<strong>in</strong>g many antibiotics. In contrast to the <strong>in</strong>nermembrane, the outer membrane is not energized by a proton gradient andATP is not available <strong>in</strong> the periplasm. The lack of direct energy sourcesmay complicate transport processes across the outer membrane.Nevertheless, nutrients are taken up from the environment and prote<strong>in</strong>s,<strong>in</strong>clud<strong>in</strong>g tox<strong>in</strong>s and hydrolytic enzymes, are secreted.Most nutrients pass the outer membrane by passive diffusion via outermembrane prote<strong>in</strong>s, collectively called por<strong>in</strong>s, which form large openchannels <strong>in</strong> the outer membrane. Hence, <strong>in</strong> this case, energy availability isnot an issue. However, diffusion is an option only when the extracellularconcentration of the solute is high. The uptake of nutrients that are toodilute <strong>in</strong> the environment or whose size exceeds the exclusion limit of thepor<strong>in</strong>s is dependent on specific receptors and requires energy. The energysource utilized is the proton-motive force across the <strong>in</strong>ner membrane,which is coupled to the transport process <strong>in</strong> the outer membrane via acomplex of three prote<strong>in</strong>s, the TonB complex. The receptors <strong>in</strong>volved arecalled TonB-dependent family (Tdf) members.In the vertebrate host, iron is sequestered by the iron-transport and -storageprote<strong>in</strong>s transferr<strong>in</strong> and lactoferr<strong>in</strong>. Hence, the concentration of free iron isextremely low and restricts microbial growth, a mechanism known asnutritional immunity. Many Gram-negative pathogens respond to ironlimitation by the production and secretion of small iron-chelat<strong>in</strong>gcompound, called siderophores, which b<strong>in</strong>d ferric ions with very highaff<strong>in</strong>ity. In addition, they produce Tdf receptors for the uptake of ferricsiderophorecomplexes. Other pathogens, <strong>in</strong>clud<strong>in</strong>g Neisseria men<strong>in</strong>gitidis,do not produce siderophores, but they produce receptors for the ironb<strong>in</strong>d<strong>in</strong>gprote<strong>in</strong>s of the host.S<strong>in</strong>ce efficient iron acquisition is an important virulence factor, it has beenstudied extensively <strong>in</strong> many pathogens. However, nutritional immunity <strong>in</strong>the host is not restricted to iron limitation. Also other metals, <strong>in</strong>clud<strong>in</strong>gz<strong>in</strong>c, manganese and nickel, can be limit<strong>in</strong>g <strong>in</strong> the host, which responds to<strong>in</strong>fections by the production of metal-b<strong>in</strong>d<strong>in</strong>g prote<strong>in</strong>s, such asmetallothione<strong>in</strong>s and calprotect<strong>in</strong>. How these metals are transported acrossthe outer membrane is largely unknown.N. men<strong>in</strong>gitidis normally lives as a commensal <strong>in</strong> the upper respiratorytract of up to 20% of the population but occasionally causes sepsis anmen<strong>in</strong>gitis. A broadly cross-protective vacc<strong>in</strong>e is not available. Thepresence of 12 Tdf receptors has been identified by analyz<strong>in</strong>g the availablegenome sequences. Five of these receptors have well-def<strong>in</strong>ed roles <strong>in</strong> ironacquisition and their expression is <strong>in</strong>duced under iron limitation.Microarray studies revealed that the expression of several other Tdfreceptors is unresponsive to iron availability; hence, we considered thepossibility that these receptors are <strong>in</strong>volved <strong>in</strong> the uptake of other metals.We have studied the response of N. men<strong>in</strong>gitidis to z<strong>in</strong>c limitation andfound that the expression of two Tdf receptors is specifically <strong>in</strong>ducedunder those conditions. We have demonstrated that these receptors are<strong>in</strong>volved <strong>in</strong> z<strong>in</strong>c acquisition and identified their ligands. The resultsdemonstrate how N. men<strong>in</strong>gitidis evades nutritional immunity imposed bythe metal-b<strong>in</strong>d<strong>in</strong>g prote<strong>in</strong>s of the host. The receptors <strong>in</strong>volved areattractive vacc<strong>in</strong>e candidates.ISV09Orig<strong>in</strong>s and proliferation of L-form (cell-wall deficient)Bacillus subtilisP. Domínguez-Cuevas, R. Mercier, Y. Kawai, J. Err<strong>in</strong>gton*Newcastle University, Centre for Bacterial Cell Biology, Institute for Celland Molecular Biosciences, Newcastle upon Tyne, United K<strong>in</strong>gdom.The cell wall is a def<strong>in</strong><strong>in</strong>g structure of bacterial cells. It provides aprotective outer shell and is crucial <strong>in</strong> pathogenesis as well as the target forimportant antibiotics. Synthesis of the wall is organised by cytoskeletalprote<strong>in</strong>s homologous to tubul<strong>in</strong> (FtsZ) and act<strong>in</strong> (MreB). Because all majorbranches of the bacterial l<strong>in</strong>eage possess both wall and cytoskeleton, thesewere probably present <strong>in</strong> the last common ancestor of the bacteria. L-formsare unusual variants of bacteria that lack the wall and are found <strong>in</strong> variousspecialised habitats, possibly responsible for a range of chronic andpersistent diseases. We have developed a model system for study<strong>in</strong>g the L-form state <strong>in</strong> Bacillus subtilis (Leaver et al., 2009, Nature 457, 849-53).Molecular genetic analysis has revealed a number of discrete stepsrequired for the transition from the walled to the non-walled state(Domnguez-Cuevas et al., <strong>2012</strong>, Mol Microbiol 83, 52-66). Unexpectedly,it has also shown that proliferation of L-forms is completely <strong>in</strong>dependentof the normally essential FtsZ or MreB cytoskeletal systems and occurs bya membrane blebb<strong>in</strong>g or tubulation process. Genetic analysis has identifiedfactors required for proliferation of L-forms, and so far these results po<strong>in</strong>tto membrane dynamics as be<strong>in</strong>g of critical importance. L-forms mayprovide an <strong>in</strong>terest<strong>in</strong>g model for consider<strong>in</strong>g how primitive cellsproliferated before the <strong>in</strong>vention of the cell wall.ISV10Positive regulation of cell division site position<strong>in</strong>g <strong>in</strong> bacteriaby a ParA prote<strong>in</strong>L. Søgaard-AndersenMax-Planck-Institut für terrestrische Mikrobiologie, Marburg, Germany.In all cells, accurate position<strong>in</strong>g of the division site is essential forgenerat<strong>in</strong>g appropriately-sized daughter cells with a correct chromosomenumber. In bacteria, cell division generally occurs at midcell and <strong>in</strong>itiateswith assembly of the tubul<strong>in</strong> homologue FtsZ <strong>in</strong>to a circumferential r<strong>in</strong>glikestructure, the Z-r<strong>in</strong>g, underneath the cell membrane at the <strong>in</strong>cipientdivision site. Subsequently, FtsZ recruits the rema<strong>in</strong><strong>in</strong>g components of thedivision mach<strong>in</strong>ery needed to carry out cytok<strong>in</strong>esis. Thus, the position ofZ-r<strong>in</strong>g formation dictates the division site. Consistently, all known systemsthat regulate position<strong>in</strong>g of the division site control Z-r<strong>in</strong>g position<strong>in</strong>g.These systems act as negative regulators to <strong>in</strong>hibit Z-r<strong>in</strong>g formation at thecell poles and over the nucleoid, leav<strong>in</strong>g only midcell free for Z-r<strong>in</strong>gformation. Here we show that the ParA homologue PomZ positivelyregulates Z-r<strong>in</strong>g position<strong>in</strong>g <strong>in</strong> Myxococcus xanthus. Lack of PomZ results<strong>in</strong> division defects, a reduction <strong>in</strong> Z-r<strong>in</strong>g formation, and abnormalposition<strong>in</strong>g of the few Z-r<strong>in</strong>gs formed. PomZ localization is cell cycleregulated and culm<strong>in</strong>ates at midcell before and <strong>in</strong>dependently of FtsZsuggest<strong>in</strong>g that PomZ recruits FtsZ to midcell. FtsZ alone does notpolymerize, however, FtsZ polymerization is directly stimulated by PomZ<strong>in</strong> vitro. Thus, PomZ positively regulates position<strong>in</strong>g of the division site byrecruit<strong>in</strong>g FtsZ and provid<strong>in</strong>g positional <strong>in</strong>formation for Z-r<strong>in</strong>g formationand coupl<strong>in</strong>g it to cell cycle progression. Models will be discussed for howPomZ identifies midcell.ISV11Integration of signals <strong>in</strong> the regulation of bacterial nitrogenassimilationA.J. N<strong>in</strong>faUniversity of Michigan Medical School, Department of BiologicalChemistry, Ann Arbor, MI, United StatesIn bacteria, nitrogen assimilation is coord<strong>in</strong>ated with other aspects ofmetabolism and cellular energy status. Three major signals are known tocontrol the expression of nitrogen regulated genes and the activity of theenzyme glutam<strong>in</strong>e synthetase, which plays a key role <strong>in</strong> the assimilation ofthe preferred nitrogen source, ammonia. These three signals are (i)glutam<strong>in</strong>e, (ii) a-ketoglutarate, and (iii) the ratio of ATP to ADP, which isan <strong>in</strong>dicator of the cellular adenylylate energy charge. In this presentation,I will review our understand<strong>in</strong>g of how these signals function to controlnitrogen assimilation <strong>in</strong> Escherichia coli.The expression of nitrogen-regulated (Ntr) genes <strong>in</strong> E. coli is controlled bya cascade-type system consist<strong>in</strong>g of two l<strong>in</strong>ked covalent modificationcycles, <strong>in</strong> which the downstream cycle is comprised of a two-componentregulatory system that directly controls gene expression. The regulation ofglutam<strong>in</strong>e synthetase activity is also controlled by a cascade-type systemcomprised of two l<strong>in</strong>ked covalent modification cycles, <strong>in</strong> which thedownstream cycle is comprised of glutam<strong>in</strong>e synthetase and the enzymethat controls its activity by reversible adenylylation. The two signall<strong>in</strong>gsystems are connected, as the upstream cycle for both systems is the same.In this upstream covalent modification cycle, the PII signal transductionBIOspektrum | Tagungsband <strong>2012</strong>
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152OTP065The role of GvpM in gas ve
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154OTP074Comparison of Faecal Cultu
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156OTP084The Use of GFP-GvpE fusion
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158compared to 20 ºC. An increase
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160characterised this plasmid in de
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162Streptomyces sp. strain FLA show
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164The study results indicated that
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166have shown direct evidences, for
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168biosurfactant. The putative lipo
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170the absence of legally mandated
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172where lowest concentrations were
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174PSV008Physiological effects of d
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176of pH i in vivo using the pH sen
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178PSP010Crystal structure of the e
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180PSP018Screening for genes of Sta
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182In order to overproduce all enzy
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184substrate specific expression of
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186potential active site region. We
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188PSP054Elucidation of the tetrach
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190family, but only one of these, t
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192network stabilizes the reactive
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194conditions tested. Its 2D struct
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196down of RSs2430 influences the e
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198demonstrating its suitability as
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200RSP025The pH-responsive transcri
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202attracted the attention of molec
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204A (CoA)-thioester intermediates.
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206Ser46~P complex. Additionally, B
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208threat to the health of reefs wo
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210their ectosymbionts to varying s
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212SMV008Methanol Consumption by Me
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214determined as a function of the
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216Funding by BMWi (AiF project no.
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218broad distribution in nature, oc
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220SMP027Contrasting assimilators o
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222growing all over the North, Cent
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224SMP044RNase J and RNase E in Sin
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226labelled hydrocarbons or potenti
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228SSV009Mathematical modelling of
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230SSP006Initial proteome analysis
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232nine putative PHB depolymerases
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234[1991]. We were able to demonstr
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236of these proteins are putative m
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238YEV2-FGMechanistic insight into
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240 AUTORENAbdel-Mageed, W.Achstett
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242 AUTORENFarajkhah, H.HMP002Faral
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244 AUTORENJung, Kr.Jung, P.Junge,
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246 AUTORENNajafi, F.MEP007Naji, S.
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249van Dijk, G.van Engelen, E.van H
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251Eckhard Boles von der Universit
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253Anna-Katharina Wagner: Regulatio
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255Vera Bockemühl: Produktioneiner
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257Meike Ammon: Analyse der subzell
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springer-spektrum.deDas große neue