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. 2006 May;72(5):3626–3636. doi: 10.1128/AEM.72.5.3626-3636.2006

TABLE 1.

Primer sequences used in this study for specific amplification of 18S rRNA gene sequences from environmental DNAa

Primer set Primer Sequence (5′-3′) Reference
1 EukA AAC CTG GTT GAT CCT GCC AGT 51
EukB TGA TCC TTC TGC AGG TTC ACC TAC 51
2 Euk82F GAA DCT GYG AAY GGC TC 40
U1391R GGG CGG TGT GTA CAA RGR 37
3 Euk360F CGG AGA RGG MGC MTG AGA 51
U1517R ACG GCT ACC TTG TTA CGA CTT 66
4 18S-6-Cil-F AAY CTG GTT GAT CCT GCC AG 28
18S-1101-Cil-R AGG YTR AGG TCT CGT TCG TT 28
a

Mixed base sites are designated according to the IUB code. F, forward; R, reverse; Cil, ciliate specific; Euk, eukaryote specific; U, universal. The numbers refer to Escherichia coli 16S rRNA gene positions. Primer EukA is a forward primer referring to Saccharomyces cerevisiae 18S rRNA gene positions 2 to 22. Primer EukB is a reverse primer referring to S. cerevisiae 18S rRNA gene positions 1795 to 1772. In the OTU analysis of the pooled data sets only overlapping regions were considered in each case. A figure showing the fragment overlaps between the different primer sets is provided in the supplemental material.