电子供体和受体条件对腐败希瓦氏菌200还原脱卤四氯化碳的影响

Effects of electron donor and acceptor conditions on reductive dehalogenation of tetrachloromethane by Shewanella putrefaciens 200.

作者信息

Picardal F, Arnold R G, Huey B B

机构信息

Department of Civil Engineering and Engineering Mechanics, University of Arizona, Tucson 85721.

出版信息

Appl Environ Microbiol. 1995 Jan;61(1):8-12. doi: 10.1128/aem.61.1.8-12.1995.

Abstract

Shewanella putrefaciens 200 is a nonfermentative bacterium that is capable of dehalogenating tetrachloromethane to chloroform and other, unidentified products under anaerobic conditions. Since S. putrefaciens 200 can respire anaerobically by using a variety of terminal electron acceptors, including NO3-, NO2-, and Fe(III), it provides a unique opportunity to study the competitive effects of different electron acceptors on dehalogenation in a single organism. The results of batch studies showed that dehalogenation of CT by S. putrefaciens 200 was inhibited by O2, 10 mM NO3-, and 3 mM NO2-, but not by 15 mM Fe(III), 15 mM fumarate, or 15 mM trimethylamine oxide. Using measured O2, Fe(III), NO2-, and NO3- reduction rates, we developed a speculative model of electron transport to explain inhibition patterns on the basis of (i) the kinetics of electron transfer at branch points in the electron transport chain, and (ii) possible direct inhibition by nitrogen oxides. In additional experiments in which we used 20 mM lactate, 20 mM glucose, 20 mM glycerol, 20 mM pyruvate, or 20 mM formate as the electron donor, dehalogenation rates were independent of the electron donor used. The results of other experiments suggested that sufficient quantities of endogenous substrates were present to support transformation of tetrachloromethane even in the absence of an exogenous electron donor. Our results should be significant for evaluating (i) the bioremediation potential at sites contaminated with both halogenated organic compounds and nitrogen oxides, and (ii) the bioremediation potential of iron-reducing bacteria at contaminated locations containing significant amounts of iron-bearing minerals.

摘要

腐败希瓦氏菌200是一种非发酵细菌,能够在厌氧条件下将四氯化碳脱卤生成氯仿和其他未鉴定产物。由于腐败希瓦氏菌200可以利用多种末端电子受体(包括NO3-、NO2-和Fe(III))进行厌氧呼吸,它为研究单一生物体中不同电子受体对脱卤作用的竞争效应提供了独特的机会。批次研究结果表明,腐败希瓦氏菌200对四氯化碳的脱卤作用受到O2、10 mM NO3-和3 mM NO2-的抑制,但不受15 mM Fe(III)、15 mM富马酸盐或15 mM氧化三甲胺的抑制。利用测得的O2、Fe(III)、NO2-和NO3-还原速率,我们建立了一个推测性的电子传递模型,以基于以下两点解释抑制模式:(i) 电子传递链分支点处的电子转移动力学,以及 (ii) 氮氧化物可能的直接抑制作用。在另外的实验中,我们使用20 mM乳酸、20 mM葡萄糖、20 mM甘油、20 mM丙酮酸或20 mM甲酸盐作为电子供体,脱卤速率与所使用的电子供体无关。其他实验结果表明,即使在没有外源电子供体的情况下,也存在足够数量的内源性底物来支持四氯化碳的转化。我们的结果对于评估 (i) 同时受到卤代有机化合物和氮氧化物污染的场地的生物修复潜力,以及 (ii) 在含有大量含铁矿物的污染地点铁还原细菌的生物修复潜力应该具有重要意义。

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