1997
DOI: 10.1099/00221287-143-9-2983
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Ribosome analysis reveals prominent activity of an uncultured member of the class Actinobacteria in grassland soils

Abstract: A 16s rRNA-based molecular ecological study was performed to search for dominant bacterial sequences in Drentse A grassland soils (The Netherlands). In the first step, a library of 165 clones was generated from PCR-amplified 165 rDNA. By sequence comparison, clone DA079 and two other identical clones could be affiliated to a group of recently described uncultured Actinobacteria. This group contained 165 rDNA clone sequences obtained from different environments across the world. To determine whether such uncult… Show more

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Cited by 347 publications
(216 citation statements)
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References 27 publications
(42 reference statements)
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“…The clone library was not used in this work for covariation analysis because of its qualitative nature and the uncertainty of its reproducibility (25)(26)(27). However, with the rapid development of high-throughput sequencing techniques (12,28), sequencing-based analysis will eventually become quantitative and cost-effective enough for this type of analysis.…”
Section: Discussionmentioning
confidence: 99%
“…The clone library was not used in this work for covariation analysis because of its qualitative nature and the uncertainty of its reproducibility (25)(26)(27). However, with the rapid development of high-throughput sequencing techniques (12,28), sequencing-based analysis will eventually become quantitative and cost-effective enough for this type of analysis.…”
Section: Discussionmentioning
confidence: 99%
“…Universal bacterial primers: 8F (5 0 -CACGGATCCAGAC TTTGAT(C/T)(A/C)TGGCTCAG-3 0 ) and 1512R (5 0 -GTG AAGCTTACGG(C/T)TAGCTTGTTACGACTT-3 0 ), based on Escherichia coli positions, were used to amplify internal fragments of 16S rRNA gene (Felske et al, 1997). Eight microliters of a bacterial suspension was transferred to a sterile thin-walled PCR tube.…”
Section: Identification Of Egg Mass-degrading Bacteriamentioning
confidence: 99%
“…Universal bacterial primers 8f and 1512r (Felske et al, 1997) were used to amplify internal fragments of the 16S rRNA gene of strain MM2LB T . Purified PCR products were sequenced with primers 8f, 534r, 968f and 1512r as described in detail by Raats & Halpern (2007).…”
mentioning
confidence: 99%