FULL POSTER SESSION ABSTRACTS668. Population shifts and mating-type heterokaryosis in Aspergillus flavus. Rodrigo A. Olarte 1 , Bruce W. Horn 2 , Carolyn J. Worthington 1 , Rakhi Singh 1 ,Ignazio Carbone 1 . 1) Department of Plant Pathology, North Carolina State University, Raleigh, NC; 2) National Peanut Research Laboratory, AgriculturalResearch Service, U.S. Department of Agriculture, Dawson, GA.Aspergillus flavus is a heterothallic fungal pathogen of many economically important crops worldwide. We sampled A. flavus strains from a cornfield inRocky Mount, North Carolina, USA. Plots were inoculated at tasselling with either A. flavus AF36 or NRRL 21882 (=Afla-Guard) nonaflatoxigenic biocontrolstrains, both of which are mating type MAT1-2. Subsequently, aflatoxigenic strain NRRL 3357 (MAT1-1) was applied to all plots, including control plots notinoculated with biocontrol strains. Sclerotia were harvested from infected corn ears and ninety single-ascospore isolates were obtained from ascocarpsoriginating from plots treated with AF36 and NRRL 21882. In addition, eighty A. flavus isolates were collected from soil one month after planting (beforebiocontrol application) and one year after biocontrol application, for a grand-total of 250 isolates. PCR amplification revealed grouping of isolates intothree distinct mating-type classes: MAT1-1, MAT1-2 and MAT1-1/MAT1-2. An overwhelming majority (54%) of isolates sampled prior to biocontroltreatments were heterokaryotic for mating type (MAT1-1/MAT1-2), but was shifted to only 9% of isolates from soil after biocontrol treatments; 39% ofisolates obtained from ascospores were heterokaryotic, with the remaining comprising either MAT1-1 or MAT1-2. Multilocus genotyping indicated thatascospores might have originated from Afla-Guard as a putative parent; there was no evidence of AF36 or NRRL 3357 in ascospores or in pre- or posttreatmentsoil samples, which may explain the genetic structure of the indigenous population. The vertical transmission of MAT1-1/MAT1-2 to progenyascospore isolates suggests that heterokaryosis can be maintained in subsequent generations. Furthermore, matings were performed to determinefunctionality of these MAT1-1/MAT1-2 strains and all isolates tested were strictly functional as MAT1-2. Further characterization of heterokaryons andtheir frequency in A. flavus populations may be important in understanding the adaptation of these fungi to changing environmental conditions and couldlead to better and more effective biocontrol strategies specific to a geographic region. Understanding population structure is the key to unlocking thesecrets of a successful biocontrol strain.669. Structural variation of trichothecene mycotoxins has resulted from multiple evolutionary processes in the fungal order Hypocreales. R. H. Proctor 1 ,A. M. Stanley 1 , M. G. Malmierca 2 , N. J. Alexander 1 , S. Gutiérrez 2 , S.P. McCormick 1 . 1) Bacterial Foodborne Pathogens and Mycology, USDA ARS NCAUR,Peoria, IL; 2) Universitary School of Agricultural Engineers, University of León, Ponferrada, Spain.Trichothecenes are secondary metabolites produced by fungi in at least six genera of the order Hypocreales. These metabolites are of concern becausethey are toxic to humans and other animals and can accumulate in grain used for food and feed. They also contribute to plant pathogenesis of Fusariumand to biological control activity of Trichoderma. Although all trichothecenes share the same molecular skeleton, a tricyclic structure with a12,13-epoxide,different genera produce trichothecenes that differ in patterns of oxygenation and acylation. To investigate how such structural variation has evolved, weexamined 1) variation in gene function and content in homologs of the trichothecene biosynthetic gene (TRI) cluster and 2) phylogenetic relationships ofTRI genes among trichothecene-producing genera. The results suggest that the ancestral hypocrealean TRI cluster consisted of at least seven genes,including the enzyme-encoding genes TRI4 and TRI5 responsible for synthesis of the trichothecene skeleton, the regulatory genes TRI6 and TRI10, and thetransporter gene TRI12. Phylogenetic analyses indicate that oxygenation of carbon atom 4 (C-4), which occurs in all trichothecene-producing genera, likelyarose when different genera acquired different C-4 hydroxylase genes: e.g. TRI11b in Trichoderma and Myrothecium and TRI13 in Fusarium. In contrast, C-3 oxygenation, which occurs in only one genus, likely arose by a change in function of TRI4, a gene that exists in all genera. These results, and those fromstudies of Fusarium and Trichoderma, indicate that structural variation of trichothecenes has arisen by recruitment, changes in function, and deletion ofTRI genes during evolution of the Hypocreales.670. Evidence for birth-and-death evolution and horizontal transfer of the fumonisin mycotoxin biosynthetic gene cluster in Fusarium. R.H Proctor 1 , F.Van Hove 2 , A. Susca 3 , G. Stea 3 , M. Busman 1 , T. van der Lee 4 , C. Waalwijk 4 , A. Moretti 3 , T.J.. Ward 1 . 1) Bacterial Foodborne Pathogens and Mycology, USDAARS NCAUR, Peoria, IL; 2) Earth and Life Science Institute, Université catholique de Louvain, Louvain, Belgium; 3) Institute of Sciences of Food Production,National Research Council, Bari, Italy; 4) Plant Research International B.V., Wageningen, The Netherlands.In fungi, genes required for synthesis of secondary metabolites are often clustered. The FUM gene cluster is required for synthesis of fumonisins, a familyof toxic secondary metabolites produced predominantly by species in the Fusarium (Gibberella) fujikuroi species complex (FFSC). Fumonisins are a healthand agricultural concern because their consumption is epidemiologically associated with multiple diseases in humans and other animals. Among FFSCspecies, the FUM cluster is discontinuously distributed but uniform in gene order and orientation. In this study, we demonstrate that the FUM clusterexists in at least four different genomic contexts within the FFSC and that phylogenetic relationships derived from analyses of FUM cluster genes arecorrelated with genomic context, but are inconsistent with species relationships inferred from analyses of primary-metabolism genes. In addition, analysesof synonymous site divergence suggested that FUM cluster divergence predated divergence of the FFSC. These results are not consistent with transspeciesevolution of ancestral cluster alleles or with interspecies hybridization, but suggest duplication of the cluster within an FFSC ancestor andsubsequent loss and sorting of paralogous clusters in a manner consistent with the birth-and-death model of evolution previously described for multigenefamilies. A model based on horizontal gene transfer (HGT) could also explain these observations, but seems unlikely because it requires independenttransfer events from multiple unknown donors to multiple FFSC recipients. However, analyses of phylogenetic relationships and synonymous sitedivergence provided strong evidence that F. oxysporum strain FRC O-1890 acquired the FUM cluster via a relatively recent HGT event from F. bulbicola or aclosely related species within the FFSC. These results indicate that, as with other secondary metabolite clusters, species phylogenies do not provide anadequate picture of the complex evolutionary history of the FUM cluster within Fusarium.671. Chemotype predominance in Fusarium graminearum is not directly affected by the use of the fungicides trifloxystrobin and isopyrazam. MatiasPasquali, Tiphaine Dubos, Friederike Pogoda, Lucien Hoffmann, Marco Beyer. Environment and Agro-biotechnologies Department, CRP GABRIELLIPPMANN, Belvaux, Luxembourg.Mitochondrial respiration inhibitors are effective fungicides used to control wheat diseases in Europe. Since the beginning of the monitoring ofchemotype diversity in wheat fields in Luxembourg, we are trying to identify factors involved in the shift of chemotype prevalence (nivalenol vs. 15ADONvs. 3ADON). In this study we investigated whether the use of fungicides belonging to the respiratory inhibitors complex II and III (that are used in wheatfields for treating other diseases) may play a role in selecting a specific F. graminearum chemotype. Strains from Luxembourg and from a world collectionwith isolation dates ranging from 1969 to 2011 were chemotyped by genetic means and then analysed for their sensitivity to trifloxystrobin (inhibitor ofrespiratory complex III) and isopyrazam (inhibitor of respiratory complex II) using a microplate in vitro test on conidia. The maximum level of inhibitionwhich could be obtained by trifloxystrobin ranged from 14 to 65% for the 55 strains analyzed with no complete inhibition up to a concentration of 3mM.Fortyone isolates tested for their sensitivity towards isopyrazam were insensitive with the average rate of inhibition converging towards 28%. For bothfungicides, EC50 values did not significantly depend on the chemotype, suggesting that these two fungicides do not exert a direct pressure on the selection286
FULL POSTER SESSION ABSTRACTSof chemotypes in F. graminearum. Our study also suggests that F. graminearum seems to be significantly insensitive to respiratory complex inhibitors (IIand III). Molecular mechanisms involved in the insensitivity are under investigation.672. Evolution of races within f.sp lycopersici of Fusarium oxysporum. BV. Chellappan, PM. Houterman, M. Rep, BJC. Cornelissen. Molecular PlantPathology, University of Amsterdam, SILS, Science Park 904, 1090 GE Amsterdam, The Netherlands.Three physiological races (1, 2 and 3) of Fusarium oxysporum f.sp lycopersici (Fol) have been identified based on their inability to infect tomato cultivarscarrying Fol resistance genes (I, I-2 or I-3, respectively). We wished to unravel the molecular mechanisms underlying the evolution of Fol races. It isgenerally assumed that race 2 evolved from race 1 by loss of AVR1 and that race 3 evolved from race 2 by a point mutation in AVR2, thus overcoming I andI-2 mediated resistance, respectively. We have sequenced a genomic region of approximately 100 kb containing AVR1 in race 1 isolate Fol004 andcompared it to the sequenced genome of race 2 isolate Fol4287. A genomic fragment of 30.5 kb containing AVR1 was found to be missing in Fol4287.Further analysis suggests that race 2 evolved from race 1 by deletion of this 30.5 kb fragment, most likely due to recombination between helitronsbordering the fragment. A worldwide collection of Fol isolates was subjected to PCR analysis of the AVR1 genomic region, including the two borderinghelitrons. The results suggest that, based on the deletion event that led to loss of AVR1, Fol isolates can be divided into distinct lineages that coincide withtheir geographical origin. Our results also suggest that transposable elements played a major role in the evolution of races within f.sp lycopersici ofFusarium oxysporum.673. Detection of Mitochondrial DNA Heteroplasmy in the progeny of crossed genetically divergent isolates of Arbuscular Mycorrhizal Fungi. MaryamNadimi, Ivan de la Providencia, Gabriela Rodriguez, Denis Beaudet, Moahmed Hijri. IRBV, Biological Sciences Dep., University of Montreal, Montreal, QC,Canada.Nonself fusion and nuclear genetic exchange has been documented in arbuscular mycorrhizal fungi (AMF) particularly in Glomus irregulare, which is acommon and widespread species. However, mitochondrial transmission accompanying nonself fusion of genetically divergent isolates remains unknown.We developed a series of crossing experiments between different isolates of G. irregulare, harboring genetically divergent mitochondrial DNA (mtDNA)haplotypes. We tested the hypothesis that heteroplasmy (i.e. mixture of genetically different mtDNA in a common cytoplasm) occurs in the progenies ofthe crossed isolates. Three isolates of geographically distant locations were used to investigate nonself fusions and mtDNA transmission in the progeny. Tobe able to trace the mtDNA haplotypes, we sequenced two mtDNAs of two G. irregulare isolates (DAOM-240415 and DAOM-234328) additional to thecurrent available isolate DAOM-197198. We developed isolate-specific markers in variable regions of intergenic mtDNAs (cox3-rnl) of these isolates. Threecrossing combinations in pre-symbiotic and symbiotic phases were performed. Interestingly, nonself fusion frequency was low and was usually associatedwith irregular shape and aborted spores, although normal spores were also observed. Ten progeny spores per crossing combination were genotyped usingisolate-specific markers. We showed the evidence that nonself fusion occurs between isolates originated from different continents both in pre-symbioticand symbiotic phases. Genotyping patterns of individual spores from the progenies clearly showed the presence of markers of the two parental mtDNAhaplotypes. Our results demonstrated the occurrence of mtDNA heteroplasmy in the progeny of crossed isolates. This raises the questions whethermtDNA heteroplasmy is transient or persistent in AMF? What are their consequences in evolution of AMF? Are there any conflicts of the presence ofmtDNA heteroplasmy within an individual? Further studies on vegetative compatibility and incompatibility and putative sex machinery in AMF will providenew information to explore and solve these questions and thereby advance our understanding of the evolution of AMF.674. Evolution of mode of infection in the rice blast fungus and allied species. Ning Zhang 1 , Shuang Zhao 1 , Jing Luo 1 , Guohong Cai 1 , DebashishBhattacharya 2 , Bradley Hillman 1 . 1) Plant Biology and Pathology, Rutgers Univ, New Brunswick, NJ; 2) Ecology, Evolution and Natural Resources, RutgersUniv, New Brunswick, NJ.The family Magnaporthaceae contains devastating fungal cereal and grass pathogens, such as Pyricularia oryzae (Magnaporthe oryzae, rice blast fungus),Magnaporthiopsis poae (Magnaporthe poae, summer patch pathogen of turf grasses), and Gaeumannomyces graminis (take-all fungus of various cerealsand grasses), which are popular model organisms in fungal biology and host-pathogen interaction studies. Despite their ecological and economicimportance, the phylogenetic relationships among the constituent species remain ambiguous due to the lack of convincing morphological characters andpaucity of molecular data for the majority of the non-model species in the family. In this study, our multilocus phylogeny suggests that both Magnaportheand Gaeumannomyces are polyphyletic genera. Therefore, a new genus, Magnaporthiopsis is proposed based on phylogeny and morphology. Thephylogeny also provides insights into fungal biology and pathogenesis. Pyricularia oryzae formed a basal clade, while Magnaporthiopsis poae andMagnaporthiopsis rhizophila formed another well-supported clade with Magnaporthiopsis incrustans (G. incrustans), G. graminis and Nakataea sigmoidea(Magnaporthe salvinii). The basal species infects both root and aerial parts of plant host, while the aerial infection capacity seems to be lost in the taxa ofthe latter clade. The study indicates that anamorphic and ecological features are more informative than the teleomorphic characters in definingmonophyletic groups among these taxa. In addition, we performed genome sequencing for 6 species in Magnaporthaceae: Magnaporthiopsis rhizophila,Magnaporthiopsis incrustans, Harpophora maydis, Nakataea sigmoidea, Ophioceras dolichostomum, and Pseudohalonectria lignicola, in order to conductphylogenomic and comparative genome analyses for both pathogenic and non-pathogenic members of this family.675. WITHDRAWN676. Population genomic analysis reveals a complex evolutionary history of Neurospora tetrasperma. Padraic Corcoran 1 , Fen Chen 2 , Martin Lascoux 1 ,Peixiang Ni 2 , Hanna Johanesson 1 . 1) Uppsala University, Uppsala, Sweden; 2) BGI, Hong Kong, Hong Kong.<strong>Fungal</strong> population genomics as a field of inquiry has seen a rapid growth in the recent years, with ability to sequence the genomes of multiple strains offungi sampled from many populations. These studies have aimed at utilizing a population genomic approach to understanding the evolutionary forces thathave had the greatest effect in shaping the genomes of fungal species. In this study, we extend the use of population genomics to help understand theevolutionary history of Neurospora tetrasperma. Neurospora tetrasperma has been the focus of much research in recent years, with most effort devotedto the study of its predominantly non-recombining mating type chromosomes. Here we present results of analysis on the whole genome resequencing of86 homokaryotic strains of N. tetrasperma, sampled from locations in England, New Zealand and Louisiana, USA, together with one strain each of the closeheterothallic species N. hispaniola and N. sitophila. These genomes were sequenced to a mean depth of between 25 to 30X coverage. Phylogenetic andpopulation structure analysis of the genomewide SNP data produced identified that the sequenced strains of N. tetrasperma belong to 5 previouslyrecognised lineages of N. tetrasperma. Comparisons of the multiple N. tetrasperma genomes with the N. sitophila, N. hispaniola and N. crassa genomesconfirmed previous observations on introgression, but also revealed signatures of introgression between the English population of N. tetrasperma and N.hispaniola. Furthermore, comparisons between the genomes of the two homokaryons isolated from each heterokaryon revealed a large number of<strong>27th</strong> <strong>Fungal</strong> <strong>Genetics</strong> <strong>Conference</strong> | 287
- Page 1:
Asilomar Conference GroundsMarch 12
- Page 7 and 8:
SCHEDULE OF EVENTSFriday, March 157
- Page 10 and 11:
EXHIBITSThe following companies hav
- Page 12 and 13:
CONCURRENT SESSIONS SCHEDULESWednes
- Page 14:
CONCURRENT SESSIONS SCHEDULESWednes
- Page 17 and 18:
CONCURRENT SESSIONS SCHEDULESThursd
- Page 19:
CONCURRENT SESSIONS SCHEDULESFriday
- Page 22 and 23:
CONCURRENT SESSIONS SCHEDULESSaturd
- Page 24:
CONCURRENT SESSIONS SCHEDULESSaturd
- Page 27 and 28:
PLENARY SESSION ABSTRACTSThursday,
- Page 29 and 30:
PLENARY SESSION ABSTRACTSFriday, Ma
- Page 31 and 32:
PLENARY SESSION ABSTRACTSSaturday,
- Page 33 and 34:
CONCURRENT SESSION ABSTRACTSWednesd
- Page 35 and 36:
CONCURRENT SESSION ABSTRACTSUnravel
- Page 37 and 38:
CONCURRENT SESSION ABSTRACTSSynergi
- Page 39 and 40:
CONCURRENT SESSION ABSTRACTSWednesd
- Page 41 and 42:
CONCURRENT SESSION ABSTRACTSWednesd
- Page 43 and 44:
CONCURRENT SESSION ABSTRACTSWednesd
- Page 45 and 46:
CONCURRENT SESSION ABSTRACTSA draft
- Page 47 and 48:
CONCURRENT SESSION ABSTRACTSRegulat
- Page 49 and 50:
CONCURRENT SESSION ABSTRACTSWednesd
- Page 51 and 52:
CONCURRENT SESSION ABSTRACTSThursda
- Page 53 and 54:
CONCURRENT SESSION ABSTRACTSThursda
- Page 55 and 56:
CONCURRENT SESSION ABSTRACTSThursda
- Page 57 and 58:
CONCURRENT SESSION ABSTRACTSThursda
- Page 59 and 60:
CONCURRENT SESSION ABSTRACTSThursda
- Page 61 and 62:
CONCURRENT SESSION ABSTRACTSThe mut
- Page 63 and 64:
CONCURRENT SESSION ABSTRACTSInnate
- Page 65 and 66:
CONCURRENT SESSION ABSTRACTSThursda
- Page 67 and 68:
CONCURRENT SESSION ABSTRACTSGenome-
- Page 69 and 70:
CONCURRENT SESSION ABSTRACTSIdentif
- Page 71 and 72:
CONCURRENT SESSION ABSTRACTSFriday,
- Page 73 and 74:
CONCURRENT SESSION ABSTRACTSFriday,
- Page 75 and 76:
CONCURRENT SESSION ABSTRACTSThe Scl
- Page 77 and 78:
CONCURRENT SESSION ABSTRACTSThe rol
- Page 79 and 80:
CONCURRENT SESSION ABSTRACTSFriday,
- Page 81 and 82:
CONCURRENT SESSION ABSTRACTSCompari
- Page 83 and 84:
CONCURRENT SESSION ABSTRACTSNovel t
- Page 85 and 86:
CONCURRENT SESSION ABSTRACTSFriday,
- Page 87 and 88:
CONCURRENT SESSION ABSTRACTSEffect
- Page 89 and 90:
CONCURRENT SESSION ABSTRACTSCommon
- Page 91 and 92:
CONCURRENT SESSION ABSTRACTSSaturda
- Page 93 and 94:
CONCURRENT SESSION ABSTRACTSSeconda
- Page 95 and 96:
CONCURRENT SESSION ABSTRACTSSheddin
- Page 97 and 98:
CONCURRENT SESSION ABSTRACTSSaturda
- Page 99 and 100:
CONCURRENT SESSION ABSTRACTSSaturda
- Page 101 and 102:
CONCURRENT SESSION ABSTRACTSSaturda
- Page 103 and 104:
CONCURRENT SESSION ABSTRACTSprocess
- Page 105 and 106:
CONCURRENT SESSION ABSTRACTSSpecifi
- Page 107 and 108:
LISTING OF ALL POSTER ABSTRACTSBioc
- Page 109 and 110:
LISTING OF ALL POSTER ABSTRACTS81.
- Page 111 and 112:
LISTING OF ALL POSTER ABSTRACTS160.
- Page 113 and 114:
LISTING OF ALL POSTER ABSTRACTS239.
- Page 115 and 116:
LISTING OF ALL POSTER ABSTRACTS322.
- Page 117 and 118:
LISTING OF ALL POSTER ABSTRACTS401.
- Page 119 and 120:
LISTING OF ALL POSTER ABSTRACTSmedi
- Page 121 and 122:
LISTING OF ALL POSTER ABSTRACTS558.
- Page 123 and 124:
LISTING OF ALL POSTER ABSTRACTS640.
- Page 125 and 126:
LISTING OF ALL POSTER ABSTRACTS723.
- Page 127 and 128:
FULL POSTER SESSION ABSTRACTS5. Cha
- Page 129 and 130:
FULL POSTER SESSION ABSTRACTS13. In
- Page 131 and 132:
FULL POSTER SESSION ABSTRACTSbioche
- Page 133 and 134:
FULL POSTER SESSION ABSTRACTS30. Me
- Page 135 and 136:
FULL POSTER SESSION ABSTRACTS38. Me
- Page 137 and 138:
FULL POSTER SESSION ABSTRACTSidenti
- Page 139 and 140:
FULL POSTER SESSION ABSTRACTSsecret
- Page 141 and 142:
FULL POSTER SESSION ABSTRACTSinvolv
- Page 143 and 144:
FULL POSTER SESSION ABSTRACTSdiploi
- Page 145 and 146:
FULL POSTER SESSION ABSTRACTSSaccha
- Page 147 and 148:
FULL POSTER SESSION ABSTRACTSresist
- Page 149 and 150:
FULL POSTER SESSION ABSTRACTS96. Ce
- Page 151 and 152:
FULL POSTER SESSION ABSTRACTS104. M
- Page 153 and 154:
FULL POSTER SESSION ABSTRACTScan ex
- Page 155 and 156:
FULL POSTER SESSION ABSTRACTSturgor
- Page 157 and 158:
FULL POSTER SESSION ABSTRACTSlike p
- Page 159 and 160:
FULL POSTER SESSION ABSTRACTSIndoor
- Page 161 and 162:
FULL POSTER SESSION ABSTRACTSlength
- Page 163 and 164:
FULL POSTER SESSION ABSTRACTSA scre
- Page 165 and 166:
FULL POSTER SESSION ABSTRACTSthen q
- Page 167 and 168:
FULL POSTER SESSION ABSTRACTS170. S
- Page 169 and 170:
FULL POSTER SESSION ABSTRACTSof sup
- Page 171 and 172:
FULL POSTER SESSION ABSTRACTSis fzo
- Page 173 and 174:
FULL POSTER SESSION ABSTRACTSgrowth
- Page 175 and 176:
FULL POSTER SESSION ABSTRACTSSeq da
- Page 177 and 178:
FULL POSTER SESSION ABSTRACTS212. T
- Page 179 and 180:
FULL POSTER SESSION ABSTRACTSCompar
- Page 181 and 182:
FULL POSTER SESSION ABSTRACTSmore g
- Page 183 and 184:
FULL POSTER SESSION ABSTRACTSmolecu
- Page 185 and 186:
FULL POSTER SESSION ABSTRACTSunexpe
- Page 187 and 188:
FULL POSTER SESSION ABSTRACTSrapid
- Page 189 and 190:
FULL POSTER SESSION ABSTRACTS260. T
- Page 191 and 192:
FULL POSTER SESSION ABSTRACTSFusari
- Page 193 and 194:
FULL POSTER SESSION ABSTRACTSScienc
- Page 195 and 196:
FULL POSTER SESSION ABSTRACTS286. G
- Page 197 and 198:
FULL POSTER SESSION ABSTRACTSincomp
- Page 199 and 200:
FULL POSTER SESSION ABSTRACTSfound
- Page 201 and 202:
FULL POSTER SESSION ABSTRACTS312. I
- Page 203 and 204:
FULL POSTER SESSION ABSTRACTSall th
- Page 205 and 206:
FULL POSTER SESSION ABSTRACTSPia La
- Page 207 and 208:
FULL POSTER SESSION ABSTRACTS335. A
- Page 209 and 210:
FULL POSTER SESSION ABSTRACTS342. F
- Page 211 and 212:
FULL POSTER SESSION ABSTRACTSThis i
- Page 213 and 214:
FULL POSTER SESSION ABSTRACTSJacobs
- Page 215 and 216:
FULL POSTER SESSION ABSTRACTScalciu
- Page 217 and 218:
FULL POSTER SESSION ABSTRACTSThe ab
- Page 219 and 220:
FULL POSTER SESSION ABSTRACTSexpres
- Page 221 and 222:
FULL POSTER SESSION ABSTRACTS394. F
- Page 223 and 224:
FULL POSTER SESSION ABSTRACTS398. U
- Page 225 and 226:
FULL POSTER SESSION ABSTRACTSthe id
- Page 227 and 228:
FULL POSTER SESSION ABSTRACTS415. A
- Page 229 and 230:
FULL POSTER SESSION ABSTRACTSAcuM b
- Page 231 and 232:
FULL POSTER SESSION ABSTRACTSdiverg
- Page 233 and 234:
FULL POSTER SESSION ABSTRACTSBck1 f
- Page 235 and 236:
FULL POSTER SESSION ABSTRACTSin the
- Page 237 and 238:
FULL POSTER SESSION ABSTRACTS455. T
- Page 239 and 240: FULL POSTER SESSION ABSTRACTSor hos
- Page 241 and 242: FULL POSTER SESSION ABSTRACTSfragme
- Page 243 and 244: FULL POSTER SESSION ABSTRACTSenhanc
- Page 245 and 246: FULL POSTER SESSION ABSTRACTSassess
- Page 247 and 248: FULL POSTER SESSION ABSTRACTSmating
- Page 249 and 250: FULL POSTER SESSION ABSTRACTScommon
- Page 251 and 252: FULL POSTER SESSION ABSTRACTSOne of
- Page 253 and 254: FULL POSTER SESSION ABSTRACTScells
- Page 255 and 256: FULL POSTER SESSION ABSTRACTSof Ave
- Page 257 and 258: FULL POSTER SESSION ABSTRACTSascaro
- Page 259 and 260: FULL POSTER SESSION ABSTRACTSis a n
- Page 261 and 262: FULL POSTER SESSION ABSTRACTSand th
- Page 263 and 264: FULL POSTER SESSION ABSTRACTSCiuffe
- Page 265 and 266: FULL POSTER SESSION ABSTRACTSon oth
- Page 267 and 268: FULL POSTER SESSION ABSTRACTScopies
- Page 269 and 270: FULL POSTER SESSION ABSTRACTSChem.
- Page 271 and 272: FULL POSTER SESSION ABSTRACTS593. C
- Page 273 and 274: FULL POSTER SESSION ABSTRACTS601. P
- Page 275 and 276: FULL POSTER SESSION ABSTRACTSE.elym
- Page 277 and 278: FULL POSTER SESSION ABSTRACTSThe de
- Page 279 and 280: FULL POSTER SESSION ABSTRACTSMicrob
- Page 281 and 282: FULL POSTER SESSION ABSTRACTSchromo
- Page 283 and 284: FULL POSTER SESSION ABSTRACTSmating
- Page 285 and 286: FULL POSTER SESSION ABSTRACTSAt the
- Page 287 and 288: FULL POSTER SESSION ABSTRACTSemerge
- Page 289: FULL POSTER SESSION ABSTRACTS666. G
- Page 293 and 294: FULL POSTER SESSION ABSTRACTSthe lo
- Page 295 and 296: FULL POSTER SESSION ABSTRACTSin the
- Page 297 and 298: FULL POSTER SESSION ABSTRACTSpotent
- Page 299 and 300: FULL POSTER SESSION ABSTRACTSpoint
- Page 301 and 302: FULL POSTER SESSION ABSTRACTS716. p
- Page 303 and 304: FULL POSTER SESSION ABSTRACTSnatura
- Page 305 and 306: FULL POSTER SESSION ABSTRACTSelemen
- Page 307 and 308: KEYWORD LISTABC proteins ..........
- Page 309 and 310: KEYWORD LISThigh temperature growth
- Page 311 and 312: AUTHOR LISTBolton, Melvin D. ......
- Page 313 and 314: AUTHOR LISTFrancis, Martin ........
- Page 315 and 316: AUTHOR LISTKawamoto, Susumu... 427,
- Page 317 and 318: AUTHOR LISTNNadimi, Maryam ........
- Page 319 and 320: AUTHOR LISTSenftleben, Dominik ....
- Page 321 and 322: AUTHOR LISTYablonowski, Jacob .....
- Page 323 and 324: LIST OF PARTICIPANTSLeslie G Beresf
- Page 325 and 326: LIST OF PARTICIPANTSTim A DahlmannR
- Page 327 and 328: LIST OF PARTICIPANTSIgor V Grigorie
- Page 329 and 330: LIST OF PARTICIPANTSMasayuki KameiT
- Page 331 and 332: LIST OF PARTICIPANTSGeorgiana MayUn
- Page 333 and 334: LIST OF PARTICIPANTSNadia PontsINRA
- Page 335 and 336: LIST OF PARTICIPANTSFrancis SmetUni
- Page 337 and 338: LIST OF PARTICIPANTSAric E WiestUni