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γ-六氯环己烷在厌氧富集培养物中作为末端电子受体的应用。

Use of γ-hexachlorocyclohexane as a terminal electron acceptor by an anaerobic enrichment culture.

机构信息

Hazardous Substance Research Center/South and Southwest, Louisiana State University, Baton Rouge, LA 70803, USA.

出版信息

J Hazard Mater. 2011 Dec 15;197:204-10. doi: 10.1016/j.jhazmat.2011.09.080. Epub 2011 Sep 29.

Abstract

The use of γ-hexachlorocyclohexane (HCH) as a terminal electron acceptor via organohalide respiration was demonstrated for the first time with an enrichment culture grown in a sulfate-free HEPES-buffered anaerobic mineral salts medium. The enrichment culture was initially developed with soil and groundwater from an industrial site contaminated with HCH isomers, chlorinated benzenes, and chlorinated ethenes. When hydrogen served as the electron donor, 79-90% of the electron equivalents from hydrogen were used by the enrichment culture for reductive dechlorination of the γ-HCH, which was provided at a saturation concentration of approximately 10 mg/L. Benzene and chlorobenzene were the only volatile transformation products detected, accounting for 25% and 75% of the γ-HCH consumed (on a molar basis), respectively. The enrichment culture remained active with only hydrogen as the electron donor and γ-HCH as the electron acceptor through several transfers to fresh mineral salts medium for more than one year. Addition of vancomycin to the culture significantly slowed the rate of γ-HCH dechlorination, suggesting that a Gram-positive organism is responsible for the reduction of γ-HCH. Analysis of the γ-HCH dechlorinating enrichment culture did not detect any known chlororespiring genera, including Dehalobacter. In bicarbonate-buffered medium, reductive dechlorination of γ-HCH was accompanied by significant levels of acetogenesis as well as methanogenesis.

摘要

首次通过有机卤化物呼吸作用,利用γ-六氯环己烷(HCH)作为末端电子受体进行了富集培养。该富集培养最初是用来自受 HCH 异构体、氯化苯和氯代乙烯污染的工业场地的土壤和地下水开发的,在没有硫酸盐的 HEPES 缓冲厌氧矿物盐培养基中进行。当氢气作为电子供体时,富集培养物将来自氢气的 79-90%的电子当量用于还原脱氯γ-HCH,该物质的饱和浓度约为 10mg/L。检测到的唯一挥发性转化产物是苯和氯苯,分别占消耗的γ-HCH(按摩尔计)的 25%和 75%。通过多次转移到新鲜的矿物盐培养基中,富集培养物仅以氢气作为电子供体和γ-HCH 作为电子受体,在超过一年的时间里保持活性。向培养物中添加万古霉素会显著减缓γ-HCH 的脱氯速率,表明一种革兰氏阳性生物负责还原γ-HCH。对γ-HCH 脱氯富集培养物的分析未检测到任何已知的氯呼吸属,包括脱硫弧菌属。在碳酸氢盐缓冲培养基中,γ-HCH 的还原脱氯伴随着显著水平的产乙酸作用和产甲烷作用。

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