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Metabolism of Dichloromethane by the Strict Anaerobe Dehalobacterium formicoaceticum

机译:严格的厌氧脱甲杆菌福美考乙酸对二氯甲烷的代谢

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摘要

The metabolism of dichloromethane by Dehalobacterium formicoaceticum in cell suspensions and crude cell extracts was investigated. The organism is a strictly anaerobic gram-positive bacterium that utilizes exclusively dichloromethane as a growth substrate and ferments this compound to formate and acetate in a molar ratio of 2:1. When [13C]dichloromethane was degraded by cell suspensions, formate, the methyl group of acetate, and minor amounts of methanol were labeled, but there was no nuclear magnetic resonance signal corresponding to the carboxyl group of acetate. This finding and previously established carbon and electron balances suggested that dichloromethane was converted to methylene tetrahydrofolate, of which two-thirds was oxidized to formate while one-third gave rise to acetate by incorporation of CO2 from the medium in the acetyl coenzyme A synthase reaction. When crude desalted extracts were incubated in the presence of dichloromethane, tetrahydrofolate, ATP, methyl viologen, and molecular hydrogen, dichloromethane and tetrahydrofolate were consumed, with the concomitant formation of stoichiometric amounts of methylene tetrahydrofolate. The in vitro transfer of the methylene group of dichloromethane onto tetrahydrofolate required substoichiometric amounts of ATP. The reaction was inhibited in a light-reversible fashion by 20 μM propyl iodide, thus suggesting involvement of a Co(I) corrinoid in the anoxic dehalogenation of dichloromethane. D. formicoaceticum exhibited normal growth with 0.8 mM sodium in the medium, and crude extracts contained ATPase activity that was partially inhibited by N,N′-dicyclohexylcarbodiimide and azide. During growth with dichloromethane, the organism thus may conserve energy not only by substrate-level phosphorylation but also by a chemiosmotic mechanism involving a sodium-independent F0F1-type ATP synthase.
机译:研究了甲醛脱盐杆菌在细胞悬浮液和粗制细胞提取物中对二氯甲烷的代谢作用。该生物是严格厌氧的革兰氏阳性细菌,仅利用二氯甲烷作为生长底物,并将该化合物发酵成摩尔比为2:1的甲酸盐和乙酸盐。当[ 13 C]二​​氯甲烷被细胞悬浮液降解时,甲酸,乙酸甲酯和少量甲醇被标记,但没有对应于乙酸羧基的核磁共振信号。这一发现以及先前建立的碳和电子平衡表明,二氯甲烷已转化为四氢叶酸亚甲基,其中三分之二被氧化成甲酸酯,而三分之一则通过将来自培养基的CO2掺入乙酰辅酶A合酶反应中而产生乙酸盐。当将脱盐的粗提物在二氯甲烷,四氢叶酸,ATP,甲基紫精和分子氢的存在下孵育时,将消耗二氯甲烷和四氢叶酸,同时形成化学计量的四氢叶酸亚甲基酯。将二氯甲烷的亚甲基体外转移到四氢叶酸上需要亚化学计量的ATP。该反应以光可逆的方式被20μM的碘甲烷抑制,因此表明Co(I)皮质醇参与了二氯甲烷的缺氧脱卤作用。 D. formicoaceticum在培养基中以0.8 mM的钠表现出正常的生长,并且粗提物中含有的ATPase活性被N,N'-二环己基碳二亚胺和叠氮化物部分抑制。因此,在用二氯甲烷生长期间,该生物体不仅可以通过底物水平的磷酸化来节省能量,而且可以通过涉及钠依赖性F0F1型ATP合酶的化学渗透机制来节省能量。

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