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Evaluation of Toxic Effects of Aeration and Trichloroethylene Oxidation on Methanotrophic Bacteria Grown with Different Nitrogen Sources

机译:曝气和三氯乙烯氧化对不同氮源生长的甲烷营养细菌的毒性作用评价

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In this study we evaluated specific and nonspecific toxic effects of aeration and trichloroethylene (TCE) oxidation on methanotrophic bacteria grown with different nitrogen sources (nitrate, ammonia, and molecular nitrogen). The specific toxic effects, exerted directly on soluble methane monooxygenase (sMMO), were evaluated by comparing changes in methane uptake rates and naphthalene oxidation rates following aeration and/or TCE oxidation. Nonspecific toxic effects, defined as general cellular damage, were examined by using a combination of epifluorescent cellular stains to measure viable cell numbers based on respiratory activity and measuring formate oxidation activities following aeration and TCE transformation. Our results suggest that aeration damages predominantly sMMO rather than other general cellular components, whereas TCE oxidation exerts a broad range of toxic effects that damage both specific and nonspecific cellular functions. TCE oxidation caused sMMO-catalyzed activity and respiratory activity to decrease linearly with the amount of substrate degraded. Severe TCE oxidation toxicity resulted in total cessation of the methane, naphthalene, and formate oxidation activities and a 95% decrease in the respiratory activity of methanotrophs. The failure of cells to recover even after 7 days of incubation with methane suggests that cellular recovery following severe TCE product toxicity is not always possible. Our evidence suggests that generation of greater amounts of sMMO per cell due to nitrogen fixation may be responsible for enhanced TCE oxidation activities of nitrogen-fixing methanotrophs rather than enzymatic protection mechanisms associated with the nitrogenase enzymes.
机译:在这项研究中,我们评估了曝气和三氯乙烯(TCE)氧化对使用不同氮源(硝酸盐,氨和分子氮)生长的甲烷营养细菌的特异性和非特异性毒性作用。通过比较曝气和/或TCE氧化后甲烷吸收速率和萘氧化速率的变化,评估了直接作用于可溶性甲烷单加氧酶(sMMO)的特定毒性作用。非特异性毒性作用定义为一般的细胞损伤,方法是使用表荧光细胞染色剂组合,根据呼吸活动测量活细胞数量,并测量通气和TCE转化后甲酸的氧化活性。我们的结果表明,曝气主要破坏sMMO而不是其他一般的细胞成分,而TCE氧化产生广泛的毒性作用,破坏特定的和非特定的细胞功能。 TCE氧化导致sMMO催化的活性和呼吸活性随底物降解量线性降低。严重的TCE氧化毒性导致甲烷,萘和甲酸盐的氧化活性完全停止,而甲烷营养菌的呼吸活性降低了95%。即使与甲烷温育7天后,细胞也无法恢复,这表明在TCE产品严重毒性后,细胞恢复并非总是可能的。我们的证据表明,每个细胞由于固氮而产生的大量sMMO可能是固氮甲烷营养生物的TCE氧化活性增强的原因,而不是与固氮酶相关的酶保护机制。

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