Bedard DL, Deweerd KA
GE Corporate Research and Development, Schenectady, New York 12301.
Appl Environ Microbiol. 1998 May 1;64(5):1786-95. doi: 10.1128/AEM.64.5.1786-1795.1998.
The upper Housatonic River and Woods Pond (Lenox, Mass.), a shallow impoundment on the river, are contaminated with polychlorinated biphenyls (PCBs), the residue of partially dechlorinated Aroclor 1260. Certain PCB congeners have the ability to activate or "prime" anaerobic microorganisms in Woods Pond sediment to reductively dehalogenate the Aroclor 1260 residue. We proposed that brominated biphenyls might have the same effect and tested the priming activities of 14 mono-, di-, and tribrominated biphenyls (350 µM) in anaerobic microcosms of sediment from Woods Pond. All of the brominated biphenyls were completely dehalogenated to biphenyl, and 13 of them primed PCB dechlorination. Measured in terms of chlorine removal and decrease in the proportion of hexa- through nonachlorobiphenyls, the microbial PCB dechlorination primed by several brominated biphenyls was nearly twice as effective as that primed by chlorinated biphenyls. Congeners containing a meta bromine primed Dechlorination Process N (flanked meta dechlorination), and congeners containing an unflanked para bromine primed Dechlorination Process P (flanked para dechlorination). Two ortho-substituted congeners, 2-bromobiphenyl and 2,6-dibromobiphenyl (2-BB and 26-BB), also primed Process N dechlorination. The most effective primers were 26-BB, 245-BB, 25-3-BB, and 25-4-BB. The microbial dechlorination primed by 26-BB converted ~75% of the hexa- through nonachlorobiphenyls to tri- and tetrachlorobiphenyls in 100 days and removed ~75% of the PCBs that are most persistent in humans. These results represent a major step toward identifying an effective method for accelerating PCB dechlorination in situ. The challenge now is to identify naturally occurring compounds that are safe and effective primers.
胡萨托尼克河上游及伍兹池塘(马萨诸塞州莱诺克斯),该池塘是河流上的一个浅水库,受到多氯联苯(PCBs)污染,这些是部分脱氯的氯丹1260的残留物。某些多氯联苯同系物能够激活或“引发”伍兹池塘沉积物中的厌氧微生物,使其对氯丹1260残留物进行还原性脱卤。我们推测溴化联苯可能有相同效果,并在来自伍兹池塘沉积物的厌氧微观世界中测试了14种单溴、二溴和三溴联苯(350µM)的引发活性。所有溴化联苯都完全脱卤生成联苯,其中13种引发了多氯联苯脱氯。以氯去除量和六氯至九氯联苯比例的降低来衡量,几种溴化联苯引发的微生物多氯联苯脱氯效果几乎是氯化联苯引发效果的两倍。含有间位溴的同系物引发脱氯过程N(间位脱氯两侧),含有未邻位取代的对位溴的同系物引发脱氯过程P(对位脱氯两侧)。两种邻位取代的同系物,2 - 溴联苯和2,6 - 二溴联苯(2 - BB和26 - BB),也引发了过程N脱氯。最有效的引发剂是26 - BB、245 - BB、25 - 3 - BB和25 - 4 - BB。26 - BB引发的微生物脱氯在100天内将约75%的六氯至九氯联苯转化为三氯和四氯联苯,并去除了约75%在人体内最持久的多氯联苯。这些结果是朝着确定一种加速多氯联苯原位脱氯的有效方法迈出的重要一步。现在的挑战是确定安全有效的天然存在的引发化合物。