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dc.contributor.authorCaton, Todd M.en_US
dc.contributor.authorSantos-Caton, Ingrid R.en_US
dc.contributor.authorWitte, Lisa R.en_US
dc.contributor.authorSchneegurt, Mark A.en_US
dc.date.accessioned2012-01-24T17:49:57Z
dc.date.available2012-01-24T17:49:57Z
dc.date.issued2009-10en_US
dc.identifier19306116en_US
dc.identifierP20 RR16475en_US
dc.identifier7500663en_US
dc.identifier.citationMicrobial ecology. 2009 Oct; 58(3): 519-28.en_US
dc.identifier.issn1432-184Xen_US
dc.identifier.issn0095-3628en_US
dc.identifier.urihttp://dx.doi.org/10.1007/s00248-009-9507-y
dc.identifier.urihttp://hdl.handle.net/10057/4205
dc.descriptionClick on the DOI link below to access the article (may not be free).en_US
dc.description.abstractThe Great Salt Plains of Oklahoma is a natural inland terrestrial hypersaline environment that forms evaporite crusts of mainly NaCl. Previous work described the bacterial community through the characterization of 105 isolates from 46 phylotypes. The current report describes the archaeal community through both microbial isolation and culture-independent techniques. Nineteen distinct archaea were isolated, and ten were characterized phenetically. Included were isolates phylogenetically related to Haloarcula, Haloferax, Halorubrum, Haloterrigena, and Natrinema. The isolates were aerobic, non-motile, Gram-negative organisms and exhibited little capacity for fermentation. All of the isolates were halophilic, with most requiring at least 15% salinity for growth, and all grew at 30% salinity. The isolates were mainly mesothermic and could grow at alkaline pH (8.5). A 16S rRNA gene library was generated by polymerase chain reaction amplification of direct soil DNA extracts, and 200 clones were sequenced and analyzed. At 99% and 94% sequence identity, 36 and 19 operational taxonomic units (OTUs) were detected, respectively, while 53 and 22 OTUs were estimated by Chao1, respectively. Coverage was relatively high (100% and 59% at 89% and 99% sequence identity, respectively), and the Shannon Index was 3.01 at 99% sequence identity, comparable to or somewhat lower than hypersaline habitats previously studied. Only sequences from Euryarchaeota in the Halobacteriales were detected, and the strength of matches to known sequences was generally low, most near 90% sequence identity. Large clusters were observed that are related to Haloarcula and Halorubrum. More than two-thirds of the sequences were in clusters that did not have close relatives reported in public databases.en_US
dc.description.sponsorshipNCRR NIH HHSen_US
dc.language.isoengen_US
dc.publisherSpringer New Yorken_US
dc.relation.ispartofseriesMicrobial ecologyen_US
dc.sourceNLMen_US
dc.subjectResearch Support, N.I.H., Extramuralen_US
dc.subjectResearch Support, U.S. Gov't, Non-P.H.S.en_US
dc.subject.meshBiodiversityen_US
dc.subject.meshDNA, Archaeal/geneticsen_US
dc.subject.meshGene Libraryen_US
dc.subject.meshHalobacteriaceae/classificationen_US
dc.subject.meshOklahomaen_US
dc.subject.meshPhylogenyen_US
dc.subject.meshRNA, Ribosomal, 16S/geneticsen_US
dc.subject.meshSalinityen_US
dc.subject.meshSequence Analysis, DNAen_US
dc.subject.meshSodium Chlorideen_US
dc.subject.meshSoil Microbiologyen_US
dc.subject.meshHalobacteriaceae/geneticsen_US
dc.subject.meshHalobacteriaceae/isolation & purificationen_US
dc.titleArchaeal diversity at the great salt plains of Oklahoma described by cultivation and molecular analysesen_US
dc.typeArticleen_US
dc.description.versionpeer revieweden_US
dc.rights.holderCopyright © 2009, Springer Science+Business Media, LLCen_US


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