We added 2,5,3‘,4‘-tetrachlorobiphenyl (25-34-CB) (350 μM) to slurries of Aroclor 1260-contaminated sediment from Woods Pond (Lenox, MA) in an attempt to stimulate dechlorination of the PCBs. The slurries were incubated under methanogenic conditions at 23−25 °C and analyzed by GC/ECD and GC/MS. The 25-34-CB was stoichiometrically converted to 25-3-CB and stimulated a selective para -dechlorination, which we designate Process P, that decreased the penta- through heptachlorobiphenyls containing 2,3,4- (234-), 245-, or 2345-chlorophenyl groups by up to 83% in 12 weeks. The products were tetra- and pentachlorobiphenyls containing 23-, 25-, and 235-chlorophenyl groups, especially 25-25-CB, 23-25-CB, 24-25-CB, 235-25-CB, and 235-23-CB. Mass balances for key parent congeners and their dechlorination products ranged from 80 to 115%. No dechlorination was detected in autoclaved controls or in live controls that were not amended with 25-34-CB. We propose that the 25-34-CB selectively enriched a population of PCB-dechlorinating microorganisms that can use it as an electron acceptor and thus “primed” the PCB dechlorination. This research demonstrates for the first time a successful strategy for stimulating rapid microbial dechlorination of PCBs that have persisted in sediments for decades and lays a foundation for the development of in situ methods for bioremediation of PCBs.
No takes yet. Share an insight, caveat, or question.
Bedard et al. (1996) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: