Skip to main content
. 2003 Mar;69(3):1372–1376. doi: 10.1128/AEM.69.3.1372-1376.2003

TABLE 1.

Detection by RT-PCR of chlorocatechol dioxygenase genes from groundwater and aquifer samples retrieved from different sectors of in situ reactor columns 1a (RA4) and 1b (Z, RB3, RB4, RB5, RB7, RB9)

Sample type Operation day Gene RT-PCR products detected at the following sampling stationsa:
Z RB3 RB4 RB5 RB7 RB9 RA4
Ground water 733 Chlorocatechol 1,2-dioxygenase + + + NDb + ND ND
Chlorocatechol 2,3-dioxygenase + ND ND ND
775 Chlorocatechol 1,2-dioxygenase + + + ND ND
Chlorocatechol 2,3-dioxygenase +c ND ND
Aquifer 803 Chlorocatechol 1,2-dioxygenase +c ND
Chlorocatechol 2,3-dioxygenase +c ND
845 Chlorocatechol 1,2-dioxygenase +c ND ND + + ND
Chlorocatechol 2,3-dioxygenase + ND ND ND
859 Chlorocatechol 1,2-dioxygenase + + + + + ND
Chlorocatechol 2,3-dioxygenase + +c ND
895 Chlorocatechol 1,2-dioxygenase + + + +
Chlorocatechol 2,3-dioxygenase +
a

The sampling stations were the following distances from the reactor bottom: Z, 0 m; RB3, 0.1 m; RB4, 0.35 m; RB5, 0.8 m; RB7, 2.5 m; RB9, 5.5 m; and RA4, 0.35 m.

b

ND, not determined.

c

The RT-PCR products were cloned and screened for variety by RFLP analysis, and selected clones were sequenced.