Abstract
PCR primers targeting conserved regions of the SSU rRNA gene are commonly used in bacterial community studies. For microbes associated with eukaryotes, co-amplification of eukaryotic DNA may preclude the analysis. We present a simple and efficient PCR strategy to obtain pure bacterial rDNA amplicons from samples predominated by eukaryotic DNA.
Copyright © 2010 Elsevier B.V. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Bacteria / genetics*
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Bacteria / growth & development
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Bacteria / isolation & purification*
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DNA Primers / genetics
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DNA, Bacterial / genetics*
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DNA, Bacterial / isolation & purification*
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DNA, Ribosomal / genetics
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DNA, Ribosomal / isolation & purification
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Eukaryota / genetics*
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Eukaryota / growth & development
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Metagenomics / methods*
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Polymerase Chain Reaction / methods*
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RNA, Ribosomal, 16S / genetics
Substances
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DNA Primers
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DNA, Bacterial
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DNA, Ribosomal
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RNA, Ribosomal, 16S