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Intergenomic evolution and metabolic cross-talk between rumen and thermophilic autotrophic methanogenic archaea

机译:瘤胃和嗜热嗜热性甲状腺原型甲状腺原型甲状腺炎型甲状腺肿的代谢串扰

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Methanobrevibacter ruminantium M1 (MRU) is a rumen methanogenic archaean that can be able to utilize formate and CO2/H-2 as growth substrates. Extensive analysis on the evolutionary genomic contexts considered herein to unravel its intergenomic relationship and metabolic adjustment acquired from the genomic content of Methanothermobacter thermautotrophicus Delta H. We demonstrated its intergenomic distance, genome function, synteny homologs and gene families, origin of replication, and methanogenesis to reveal the evolutionary relationships between Methanobrevibacter and Methanothermobacter. Comparison of the phylogenetic and metabolic markers was suggested for its archaeal metabolic core lineage that might have evolved from Methanothermobacter. Orthologous genes involved in its hydrogenotrophic methanogenesis might be acquired from intergenomic ancestry of Methanothermobacter via Methanobacterium formicicum. Formate dehydrogenase (fdhAB) coding gene cluster and carbon monoxide dehydrogenase (cooF) coding gene might have evolved from duplication events within Methanobreviba cter-Methanothermobacter lineage, and fdhCD gene cluster acquired from bacterial origins. Genome-wide metabolic survey found the existence of four novel pathways viz. L-tyrosine catabolism, mevalonate pathway II, acyl-carrier protein metabolism II and glutathione redox reactions II in MRU. Finding of these pathways suggested that MRU has shown a metabolic potential to tolerate molecular oxygen, antimicrobial metabolite biosynthesis and atypical lipid composition in cell wall, which was acquainted by metabolic cross-talk with mammalian bacterial origins. We conclude that coevolution of genomic contents between Methanobrevibacter and Methanothermobacter provides a clue to understand the metabolic adaptation of MRU in the rumen at different environmental niches. (C) 2016 Elsevier Inc. All rights reserved.
机译:甲烷纤维杆菌M1(MRU)是一种瘤胃甲基甲基甲基甲基甲基甲蛋白甲基甲基甲基甲基甲基甲基甲基甲基甲基甲基甲基甲基甲基甲基甲基甲基甲基型古代甲酸甲基甲酸甲基甲基甲基型甲酸甲酸盐和CO2 / H-2作为生长底物。对甲烷热杆菌基因组δ的基因组含量揭示的进化基因组背景下考虑的进化基因组语学的广泛分析,其展示了其与甲基术δ的基因组含量,基因组函数,同时性同源物和基因家族,复制起源和甲烷生成揭示甲烷杆菌和甲烷热杆菌之间的进化关系。提出了系统发育和代谢标志物的比较,其古代代谢核心谱系可能已经从甲烷热杆菌演变。可以通过甲基杆菌甲基杆菌从甲烷热杆菌的骨髓组血液中获取涉及其氢型甲烷的正交基因。甲酸脱氢酶(FdhAb)编码基因簇和一氧化碳脱氢酶(COOF)编码基因可能已经从甲氧吡韦菌酸杆菌杆菌血丝杆菌和从细菌起源中获取的FDHCD基因簇中的复制事件。基因组的代谢调查发现了四种新颖途径的存在。 L-酪氨酸分解代谢,甲戊烷途径II,酰基载体蛋白质代谢II和MRU的谷胱甘肽氧化还原反应II。寻找这些途径表明MRU已经示出了在细胞壁中耐受分子氧,抗微生物代谢物生物合成和非典型脂质组合物的代谢潜力,其熟悉与哺乳动物的代谢串扰。我们得出结论,甲烷的甲基杆菌和甲烷热杆菌之间的基因组内容物的共同提供了一种方法,以了解MRU在不同环境核桃的瘤胃中的代谢适应。 (c)2016年Elsevier Inc.保留所有权利。

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