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首页> 外文期刊>Philosophical Transactions of the Royal Society of London, Series B. Biological Sciences >Guided cobalamin biosynthesis supports Dehalococcoides mccartyi reductive dechlorination activity
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Guided cobalamin biosynthesis supports Dehalococcoides mccartyi reductive dechlorination activity

机译:引导钴胺素的生物合成支持麦考替尼脱卤球菌的还原脱氯活性

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Dehalococcoides mccartyi strains are corrinoid-auxotrophic Bacteria and axenic cultures that require vitamin B_(12) (CN-Cbl) to conserve energy via organohalide respiration. Cultures of D. mccartyi strains BAV1, GT and FL2 grown with limiting amounts of 1 μg1~(-1) CN-Cbl quickly depleted CN-Cbl, and reductive dechlorination of polychlorinated ethenes was incomplete leading to vinyl chloride (VC) accumulation. In contrast, the same cultures amended with 25 μg l~(-1) CN-Cbl exhibited up to 2.3-fold higher dechlorination rates, 2.8–9.1-fold increased growth yields, and completely consumed growth-supporting chlorinated ethenes. To explore whether known cobamide-producing microbes supply Dehalococcoides with the required corrinoid cofactor, co-culture experiments were performed with the methanogen Methanosarcina barkeri strain Fusaro and two acetogens, Sporomusa ovata and Sporomusa sp. strain KB-1, as Dehalococcoides partner populations. During growth with H_2/CO_2, M. barkeri axenic cultures produced 4.2 + 0.1 μg l~(-1) extracellular cobamide (factor Ⅲ), whereas the Sporomusa cultures produced phenolyl- and p-cresolyl-cobamides. Neither factor III nor the phenolic cobamides supported Dehalococcoides reductive dechlorination activity suggesting that M. barkeri and the Sporomusa sp. cannot fulfil Dehalococcoides’ nutritional requirements. Dehalococcoides dechlorination activity and growth occurred in M. barkeri and Sporomusa sp. co-cultures amended with 10 mM 50,60-dimethylbenzimidazole (DMB), indicating that a cobalamin is a preferred corrinoid cofactor of strains BAV1, GT and FL2 when grown with chlorinated ethenes as electron acceptors. Even though the methanogen and acetogen populations tested did not produce cobalamin, the addition of DMB enabled guided biosynthesis and generated a cobalamin that supported Dehalococcoides’ activity and growth. Guided cobalamin biosynthesis may offer opportunities to sustain and enhance Dehalococcoides activity in contaminated subsurface environments.
机译:Dehalococcoides mccartyi菌株是类Corrinoid-营养缺陷型细菌和需要维生素B_(12)(CN-Cbl)才能通过有机卤化物呼吸节省能量的无菌培养物。限制量为1μg1〜(-1)CN-Cbl的麦卡迪氏菌BAV1,GT和FL2的培养物很快耗尽了CN-Cbl,多氯乙烯的还原脱氯作用不完全,导致氯乙烯(VC)积累。相反,用25μgl〜(-1)CN-Cbl修饰的相同培养物显示最高高达2.3倍的脱氯速率,增长了2.8-9.1倍的增长产量,并完全消耗了支持生长的氯化乙烯。为了探究已知的产生钴胺酰胺的微生物是否为Dehaloccocoides提供所需的类海藻素辅助因子,用产甲烷甲烷化甲烷菌(Mthanosarcina barkeri)Fusaro菌株和两种产乙酸原,卵形孢子菌和孢子菌菌种进行了共培养实验。菌株KB-1,作为Dehalococcoides的伙伴种群。在H_2 / CO_2的生长过程中,巴克莫氏菌的培养物产生4.2 + 0.1μgl〜(-1)的细胞外Cobamide(因子Ⅲ),而Sporomusa培养物则产生酚基和对甲酚基Cobamides。因子III和酚类cobamides都不支持Dehalococcoides的还原性脱氯活性,这表明巴克莫氏菌和Sporomusa sp。无法满足Dehalococcoides的营养要求。 Dehalococcoides的脱氯活性和生长发生在M. barkeri和Sporomusa sp。中。用10 mM 50,60-二甲基苯并咪唑(DMB)进行的共培养表明,钴胺素是BAV1,GT和FL2菌株的首选类rinrinoid辅因子,与氯化乙烯作为电子受体一起生长。即使所测试的产甲烷菌和产乙酸菌的种群不产生钴胺素,但添加DMB仍可指导生物合成,并产生了支持Dehalococcoides活性和生长的钴胺素。引导钴胺素的生物合成可能为在受污染的地下环境中维持和增强Dehaloccocoides活性提供机会。

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