†School of Biotechnology and Biomolecular Science, University of New South Wales, Kensington, Sydney 2052, Australia.
‡Department of Isotope Biogeochemistry, Helmholtz Centre for Environmental Research-UFZ, Permoser Strasse 15, Leipzig 04318, Germany.
Environ Sci Technol. 2015 Apr 7;49(7):4481-9. doi: 10.1021/es5052364. Epub 2015 Mar 24.
The role of bacteria and zerovalent iron (Fe(0)) in the degradation of chlorinated solvents in subsurface environments is of interest to researchers and remediation practitioners alike. Fe(0) used in reactive iron barriers for groundwater remediation positively interacted with enrichment cultures containing Dehalobacter strains in the transformation of halogenated methanes. Chloroform transformation and dichloromethane formation was up to 8-fold faster and 14 times higher, respectively, when a Dehalobacter-containing enrichment culture was combined with Fe(0) compared with Fe(0) alone. The dichloromethane-fermenting culture transformed dichloromethane up to three times faster with Fe(0) compared to without. Compound-specific isotope analysis was employed to compare abiotic and biotic chloroform and dichloromethane degradation. The isotope enrichment factor for the abiotic chloroform/Fe(0) reaction was large at -29.4 ± 2.1‰, while that for chloroform respiration by Dehalobacter was minimal at -4.3 ± 0.45‰. The combined abiotic/biotic dechlorination was -8.3 ± 0.7‰, confirming the predominance of biotic dechlorination. The enrichment factor for dichloromethane fermentation was -15.5 ± 1.5‰; however, in the presence of Fe(0) the factor increased to -23.5 ± 2.1‰, suggesting multiple mechanisms were contributing to dichloromethane degradation. Together the results show that chlorinated methane-metabolizing organisms introduced into reactive iron barriers can have a significant impact on trichloromethane and dichloromethane degradation and that compound-specific isotope analysis can be employed to distinguish between the biotic and abiotic reactions involved.
细菌和零价铁(Fe(0))在地下环境中氯化溶剂降解中的作用引起了研究人员和修复从业者的共同关注。用于地下水修复的反应性铁屏障中的 Fe(0) 与含有 Dehalobacter 菌株的富集培养物积极相互作用,促进卤代甲烷的转化。与单独使用 Fe(0)相比,当含有 Dehalobacter 的富集培养物与 Fe(0)结合时,三氯甲烷的转化速度提高了 8 倍,二氯甲烷的形成速度提高了 14 倍。与没有 Fe(0)相比,二氯甲烷发酵培养物使用 Fe(0)的二氯甲烷转化速度提高了三倍。采用化合物特异性同位素分析来比较非生物和生物三氯甲烷和二氯甲烷的降解。非生物三氯甲烷/Fe(0)反应的同位素富集因子很大,为-29.4±2.1‰,而 Dehalobacter 呼吸作用的三氯甲烷的同位素富集因子最小,为-4.3±0.45‰。组合的非生物/生物脱氯作用的同位素富集因子为-8.3±0.7‰,证实了生物脱氯作用的主导地位。二氯甲烷发酵的富集因子为-15.5±1.5‰;然而,在 Fe(0)存在下,该因子增加到-23.5±2.1‰,这表明有多种机制有助于二氯甲烷的降解。总的来说,这些结果表明,引入反应性铁屏障中的氯化甲烷代谢生物体会对三氯甲烷和二氯甲烷的降解产生重大影响,并且可以采用化合物特异性同位素分析来区分所涉及的生物和非生物反应。