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首页> 外文期刊>Applied and Environmental Microbiology >Chloroform degradation in methanogenic methanol enrichment cultures and by Methanosarcina barkeri 227.
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Chloroform degradation in methanogenic methanol enrichment cultures and by Methanosarcina barkeri 227.

机译:在产甲烷的甲醇富集培养物中和由巴氏甲烷菌(Methanosarcina barkeri)227降解氯仿。

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The effects of methanol addition and consumption on chloroform degradation rate and product distribution in methanogenic methanol enrichment cultures and in cultures of Methanosarcina barkeri 227 were investigated. Degradation of chloroform with initial concentrations up to 27.3 microM in enrichment cultures and 4.8 microM in pure cultures was stimulated by the addition of methanol. However, methanol consumption was inhibited by as little as 2.5 microM chloroform in enrichment cultures and 0.8 microM chloroform in pure cultures, suggesting that the presence of methanol, not its exact concentration or consumption rate, was the most significant variable affecting chloroform degradation rate. Methanol addition also significantly increased the number of moles of dichloromethane produced per mole of chloroform consumed. In enrichment cultures, the number of moles of dichloromethane produced per mole of chloroform consumed ranged from 0.7 (methanol consumption essentially uninhibited) to 0.35 (methanol consumption significantly inhibited) to less than 0.2 (methanol not added to the culture). In pure cultures, the number of moles of dichloromethane produced per mole of chloroform consumed was 0.47 when methanol was added and 0.24 when no methanol was added. Studies with [14C]chloroform in both enrichment and pure cultures confirmed that methanol metabolism stimulated dichloromethane production compared with CO2 production. The results indicate that while the addition of methanol significantly stimulated chloroform degradation in both methanogenic methanol enrichment cultures and cultures of M. barkeri 227, the prospects for use of methanol as a growth substrate for anaerobic chloroform-degrading systems may be limited unless the increased production of undesirable chloroform degradation products and the inhibition of methanol consumption can be mitigated.
机译:研究了甲醇的添加和消耗量对甲烷生成甲烷富集培养物和巴氏甲烷八叠球菌培养物中氯仿降解速率和产物分布的影响。加入甲醇可刺激富集培养物中初始浓度最高为27.3 microM的氯仿降解,而纯培养物中初始浓度高达4.8 microM的降解。但是,富集培养中的甲醇消耗仅受到2.5 microM氯仿的抑制,纯培养物中甲醇的消耗被抑制至0.8 microM氯仿,表明甲醇的存在而不是其确切浓度或消耗速率是影响氯仿降解速率的最重要变量。甲醇的添加还显着增加了每消耗一摩尔氯仿产生的二氯甲烷的摩尔数。在富集培养中,每消耗一摩尔氯仿产生的二氯甲烷摩尔数为0.7(基本上不抑制甲醇消耗)至0.35(明显抑制甲醇消耗)至小于0.2(未向培养物中添加甲醇)。在纯培养物中,当添加甲醇时,每消耗一摩尔氯仿产生的二氯甲烷摩尔数为0.47,而当不添加甲醇时为0.24。用[14C]氯仿进行浓缩和纯培养的研究证实,与CO2产生相比,甲醇代谢刺激了二氯甲烷的产生。结果表明,尽管在产甲烷的甲醇富集培养物和巴克莫里氏菌227的培养物中添加甲醇均能显着刺激氯仿的降解,但除非增加产量,否则将甲醇用作厌氧氯仿降解系统生长底物的前景可能会受到限制。可以减轻不希望有的氯仿降解产物的产生和甲醇消耗的抑制。

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