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. 2007 Feb 16;73(8):2513–2521. doi: 10.1128/AEM.02909-06

TABLE 1.

16S rRNA gene-targeted PCR screening of an Aroclor 1260-dechlorinating JN culture for known dechlorinating bacterial groups

Dechlorinating group PCR result at DNA dilution showna
Positive control Primersb
Direct
Nested
U 1/10 1/100 U 1/5 1/50
Dehalococcoides + + + D. ethenogenes 195 DHC 1 (F) and DHC 1377 (R) (31)
Anaeromyxobacter Anaeromyxobacter dehalogenans strain 2CP-C A60-86F and A447-465R (21)
Desulfitobacterium Desulfitobacterium sp. strain Viet 1 Dd1 (F) and Dd2 (R) (23)
Desulfuromonas Desulfuromonas michiganensis strain BB1 BB1F and BB1R (41)
Dehalobacter Dehalobacter sp. deb 179f and deb 1007r (54)
Sulfurospirillum (formerly Dehalospirillum) Sulfurospiriillum multivorans JPDF 121 and JPDR 557 (50)
Sulfurospirillum halorespirans DHSPM 576 and DHSPM 1210c
Geobacter (SZ type) Geobacter lovleyi strain SZ 196F and 999R (58)
o-17/DF-1-type Chloroflexi NDd Clone of o-17 16S rRNA gene 14F (22) and 1265R (61)
a

U, undiluted.

b

References for some primers are shown in parentheses.

c

R. C. Ebersole and E. R. Hendrickson, U.S. patent application 20030077601.

d

ND, not determined. Nested PCR was not performed because the 14F primer shares the same recognition site as the bacterial universal primer 27F used in the initial round of PCR amplification.