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在还原态铁氧化物存在下四氯化碳的强化厌氧生物转化

Enhanced anaerobic biotransformation of carbon tetrachloride in the presence of reduced iron oxides.

作者信息

Kim Sanggoo, Picardal Flynn W

机构信息

School of Public and Environmental Affairs, Indiana University, Bloomington, IN 47405, USA.

出版信息

Environ Toxicol Chem. 1999 Oct;18(10):2142-2150. doi: 10.1002/etc.5620181005.

Abstract

Rates of anaerobic transformation of carbon tetrachloride (CT) by the facultative anaerobe Shewanella putrefaciens 200 were increased by the presence of Fe(III)-containing minerals. In batch reactors with amorphous, Fe(III)-hydroxide and S. putrefaciens, CT transformation rates could be modeled by a first-order expression in which the pseudo-first-order rate constant was linearly proportional to the initial concentration of Fe(III)-oxide. Subsequent measurement of soluble and acid-extractable Fe(II) showed that increased CT transformation rates were proportional to microbially reduced, surface-bound Fe(II), rather than soluble Fe(II). In biomimetic experiments using 20 mM dithiothreitol (DTT) as a reductant, rates of transformation of CT by DTT were low in the absence of Fe(III)-oxides. However, in the presence of iron oxides, DTT was able to transform CT at elevated rates. Results again strongly suggested that surface-bound Fe(II) was primarily responsible for the reductive transformation of CT. Results suggested that the surface area of the iron mineral determines the rate of CT transformation by affecting the extent of iron reduction. Chloroform (CF) was the only transformation product identified and production of CF was nonstoichiometric. In microbial and abiotic experiments with Fe(III) oxides, the percentage of the transformed CT recovered as CF decreased even though the rate and extent of CT transformation was increased. Overall, our results have important implications for an improved understanding of possible microbial and geochemical interactions in the environmental transformation of chlorinated organic pollutants and for modeling of CT transformation rates in anaerobic, iron-bearing sediments.

摘要

兼性厌氧菌腐败希瓦氏菌200对四氯化碳(CT)的厌氧转化速率因含铁(III)矿物的存在而提高。在含有无定形氢氧化铁(III)和腐败希瓦氏菌的间歇式反应器中,CT的转化速率可用一级表达式进行模拟,其中伪一级速率常数与铁(III)氧化物的初始浓度呈线性比例关系。随后对可溶性和酸可提取的铁(II)的测量表明,CT转化速率的提高与微生物还原的表面结合铁(II)成正比,而非可溶性铁(II)。在使用20 mM二硫苏糖醇(DTT)作为还原剂的仿生实验中,在没有铁(III)氧化物的情况下,DTT对CT的转化速率很低。然而,在有铁氧化物存在的情况下,DTT能够以较高的速率转化CT。结果再次有力地表明,表面结合的铁(II)是CT还原转化的主要原因。结果表明,铁矿物的表面积通过影响铁还原的程度来决定CT的转化速率。氯仿(CF)是唯一鉴定出的转化产物,且CF的生成是非化学计量的。在使用铁(III)氧化物的微生物和非生物实验中,尽管CT的转化速率和程度有所提高,但作为CF回收的转化CT的百分比却下降了。总体而言,我们的结果对于更好地理解氯化有机污染物环境转化中可能的微生物和地球化学相互作用以及对厌氧含铁沉积物中CT转化速率的建模具有重要意义。

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