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Anaerobic Biodegradation of 245-Trichlorophenoxyacetic Acid in Samples from a Methanogenic Aquifer: Stimulation by Short-Chain Organic Acids and Alcohols

机译:产甲烷层中样品中245-三氯苯氧基乙酸的厌氧生物降解:短链有机酸和醇的刺激

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摘要

The herbicide 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) was dehalogenated in samples from a methanogenic aquifer to form 2,4- and 2,5-dichlorophenoxyacetic acids as the first detected intermediates. Further incubation of the aquifer slurries resulted in the formation of several intermediates including monochlorophenoxyacetic acids, di- and monochlorophenols, as well as phenol. No transformation of the parent substrate or production of intermediates was detected in autoclaved controls. The pattern of intermediate formation suggested that the anaerobic degradation of 2,4,5-T proceeded by a series of sequential dehalogenation steps with side-chain cleavage reactions occurring at some point before ring cleavage. The addition of short-chain organic acids or alcohols stimulated the onset and rate of 2,4,5-T dehalogenation and decreased the amount of parent substrate still detectable as halogenated intermediates at the end of the experiment. Sulfate addition had the opposite effect on dehalogenation regardless of whether supplemental carbon was added to the aquifer slurries. The inhibitory effect of sulfate on dehalogenation could sometimes be relieved with molybdate, although this effect seemed to be related to the supplemental carbon compound that was used.
机译:将除草剂2,4,5-三氯苯氧基乙酸(2,4,5-T)从产甲烷的含水层中脱卤,以形成2,4-和2,5-二氯苯氧基乙酸作为最早检测到的中间体。含水层浆液的进一步温育导致形成了几种中间体,包括一氯苯氧基乙酸,二氯和一氯苯酚以及苯酚。在高压灭菌的对照中未检测到母体底物的转化或中间体的产生。中间体形成的模式表明2,4,5-T的厌氧降解是通过一系列连续的脱卤步骤进行的,侧链裂解反应发生在环裂解之前的某个位置。在实验结束时,添加短链有机酸或醇刺激了2,4,5-T脱卤反应的发生和速率,并减少了仍可检测为卤代中间体的母体底物的量。无论是否向含水层浆液中添加了补充碳,添加硫酸盐对脱卤都有相反的作用。硫酸盐对脱卤的抑制作用有时可以用钼酸盐减轻,尽管这种作用似乎与所用的补充碳化合物有关。

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