• Media type: E-Article
  • Title: Oligonucleotide Microarray for 16S rRNA Gene-Based Detection of All Recognized Lineages of Sulfate-Reducing Prokaryotes in the Environment
  • Contributor: Loy, Alexander; Lehner, Angelika; Lee, Natuschka; Adamczyk, Justyna; Meier, Harald; Ernst, Jens; Schleifer, Karl-Heinz; Wagner, Michael
  • imprint: American Society for Microbiology, 2002
  • Published in: Applied and Environmental Microbiology
  • Language: English
  • DOI: 10.1128/aem.68.10.5064-5081.2002
  • ISSN: 0099-2240; 1098-5336
  • Keywords: Ecology ; Applied Microbiology and Biotechnology ; Food Science ; Biotechnology
  • Origination:
  • Footnote:
  • Description: <jats:title>ABSTRACT</jats:title> <jats:p> For cultivation-independent detection of sulfate-reducing prokaryotes (SRPs) an oligonucleotide microarray consisting of 132 16S rRNA gene-targeted oligonucleotide probes (18-mers) having hierarchical and parallel (identical) specificity for the detection of all known lineages of sulfate-reducing prokaryotes (SRP-PhyloChip) was designed and subsequently evaluated with 41 suitable pure cultures of SRPs. The applicability of SRP-PhyloChip for diversity screening of SRPs in environmental and clinical samples was tested by using samples from periodontal tooth pockets and from the chemocline of a hypersaline cyanobacterial mat from Solar Lake (Sinai, Egypt). Consistent with previous studies, SRP-PhyloChip indicated the occurrence of <jats:italic>Desulfomicrobium</jats:italic> spp. in the tooth pockets and the presence of <jats:italic>Desulfonema</jats:italic> - and <jats:italic>Desulfomonile</jats:italic> -like SRPs (together with other SRPs) in the chemocline of the mat. The SRP-PhyloChip results were confirmed by several DNA microarray-independent techniques, including specific PCR amplification, cloning, and sequencing of SRP 16S rRNA genes and the genes encoding the dissimilatory (bi)sulfite reductase ( <jats:italic>dsrAB</jats:italic> ). </jats:p>
  • Access State: Open Access