Toxic polychlorinated dibenzo-p-dioxins and dibenzofurans(PCDD/Fs) with chlorines substituted at the lateral 2, 3, 7, and8 positions are of great environmental concern. We investigatedthe dechlorination of 1,2,3,4,7,8-hexachlorodibenzofuran (1,2,3,4,7,8-HxCDF) and 1,2,3,4,6,7,8,9-octachlorodibenzo-p-dioxin (OCDD)by a mixed culture containingDehalococcoides ethenogenesstrain 195. The 1,2,3,4,7,8-HxCDF was dechlorinated to 1,3,4,7,8-pentachlorodibenzofuran and 1,2,4,7,8-pentachlorodibenzofuranand further to two tetrachlorodibenzofuran congeners, whichwere identified as 1,3,7,8-tetrachlorodibenzofuran and 1,2,4,8-tetrachlorodibenzofuran. Because no 2,3,7,8-substituted congenerswere formed as dechlorination products from 1,2,3,4,7,8-HxCDF, this dechlorination represents a detoxification reaction.Tetrachloroethene (PCE) and 1,2,3,4-tetrachlorobenzene (1,2,3,4-TeCB) were added as additional halogenated substrates toenhance the degree of 1,2,3,4,7,8-HxCDF dechlorination. The 1,2,3,4-TeCB enhanced the extent of dechlorination of 1,2,3,4,7,8-HxCDF approximately 3-fold compared to PCE or no additionalsubstrate amendment. No dechlorination products weredetected from OCDD. Bioremediation of PCDD/Fs by bacterialreductive dechlorination should address the pathway ofdechlorination to ensure detoxification.
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