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首页> 外文期刊>Extremophiles: Life under extreme conditions >A metabolic and genomic assessment of sugar fermentation profiles of the thermophilic Thermotogales, Fervidobacterium pennivorans
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A metabolic and genomic assessment of sugar fermentation profiles of the thermophilic Thermotogales, Fervidobacterium pennivorans

机译:嗜热热敏性糖发酵谱的代谢和基因组评估,Pennivorans

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摘要

A metabolic, genomic and proteomic assessment of Fervidobacterium pennivorans strains was undertaken to clarify the metabolic and genetic capabilities of this Thermotogales species. The type strain Ven5 originally isolated from a hot mud spa in Italy, and a newly isolated strain (DYC) from a hot spring at Ngatamariki, New Zealand, were compared for metabolic and genomic differences. The fermentation profiles of both strains on cellobiose generated similar major end products (acetate, alanine, glutamate, H-2, and CO2). The vast majority of end products produced were redox neutral, and carbon balances were in the range of 95-115%. Each strain showed distinct fermentation profiles on sugar substrates. The genome of strain DYC was sequenced and shown to have high sequence similarity and synteny with F. pennivorans Ven5 genome, suggesting they are the same species. The unique genome regions in Ven5, corresponded to genes involved in the Entner-Doudoroff pathway confirming our observation of DYC's inability to utilize gluconate. Genome analysis was able to elucidate pathways involved in production of the observed end-products with the exception of alanine and glutamate synthesis which were resolved with less clarity due to poor sequence identity and missing critical enzymes within the pathway, respectively.
机译:进行了术治疗菌株菌株的代谢,基因组和蛋白质组学评估,以阐明该热敏性物种的代谢和遗传能力。比较了从意大利的热泥水疗中心和新西兰Ngatamariki,新西兰的热弹簧中分离出的菌株毒液5,以及新西兰的热弹簧,得到代谢和基因组差异。两种菌株的发酵型材在纤维二糖产生类似的主要末端产物(醋酸盐,丙氨酸,谷氨酸,H-2和CO 2)。产生的绝大多数终端产品是氧化还原中性,碳余额在95-115%的范围内。每种菌株在糖基材上显示出不同的发酵曲线。测序菌株的基因组并显示具有高序列相似性和与F.Pennivorans Ven5基因组的同时性,表明它们是相同的物种。 Ven5的独特基因组区域,对应于涉及Entner-Doudoroff途径的基因,证实了我们观察Dyc无法使用葡萄糖酸盐。除了丙氨酸和谷氨酸合成之外,基因组分析能够阐明参与所观察到的最终产品的途径,其由于途径缺失的序列同一性和缺少途径缺失的临界酶而在较少的透明度分离。

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