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. 2000 Jul;66(7):2873–2881. doi: 10.1128/aem.66.7.2873-2881.2000

TABLE 3.

Results of PCR experiments with Mono Lake DNA extractsa

Sample
Expt
rRNA sequence obtained
Direct amplification of genomic DNA extracts with:
Two-stage amplification: reamplification of EUB amplification product with:
P2P3 amplification: reamplification of NitA-NitB amplification product with:
Laboratory A Laboratory B
No. Depth (m) EUB NitA-NitB NitD-NitB NitA-NitB NitD-NitB NOC1-NOC2 P2P3 N.euro*
4.2 1 + + + + + +
4.7 1 + + + + +
4.5 5 + + + + + + + 4.5PCR 4.5-A–4.5-E
4.8 5 + + + + + + + 4.8PCR 4.8-A–4.8-E
4.3 10 + + + + + +
4.9 10 + + + +
4.10 11 + +
4.11 12 + + + + +
4.12 12 +
4.13 13 + + + + + +
4.14 15 + + + + +
4.15 15 + + + + + +
4.16 17 + + + +
4.17 20 +
4.20 20 + +
4.18 23 + + + + + + + 4.18.4, 4.18.8 4.18-A–4.18-J
4.19 25 +
7.6 1 + ND ND
7.15 1 + + + + + + 7.15PCR 7.15-A–7.15-J
7.2 5 + + ND ND ND
7.5 5 + + + +
7.4 7 + +
7.7 10 + ND ND
7.13 10 + + + + + +
7.19 10 + + + + +
7.3 12 + + ND ND ND
7.12 13 + + + +
7.11 14 + + + +
7.1 15 + +
7.1 17 + + + +
7.18 20 + + + + + + + 7.18.5, 7.18.6 7.18-B–7.18-H
7.14 23 + + + + + +
7.17 25 + + + + + +
a

See Table 1 for primer abbreviations. The names of the rDNA sequences reflect derivation as sequenced directly from the PCR fragment (e.g., 4.5PCR) or from a cloned PCR fragment (e.g., 4.18.4). +, detection of expected size PCR fragment by agarose gel electrophoresis; −, denotes no PCR fragments detected; ND, no data due to insufficient sample to perform this analysis; N. euro*, detection of a band corresponding to the position of the N. europaea standard band in DGGE.