4.8 Article

Microbial dark matter ecogenomics reveals complex synergistic networks in a methanogenic bioreactor

期刊

ISME JOURNAL
卷 9, 期 8, 页码 1710-1722

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NATURE PUBLISHING GROUP
DOI: 10.1038/ismej.2014.256

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资金

  1. US Department of Energy Office of Science [DE-AC02-05CH11231]
  2. US Department of Energy [DE-SC0006771]
  3. Energy Biosciences Institute (EBI) at the University of Illinois Urbana-Champaign (UIUC)

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Ecogenomic investigation of a methanogenic bioreactor degrading terephthalate (TA) allowed elucidation of complex synergistic networks of uncultivated microorganisms, including those from candidate phyla with no cultivated representatives. Our previous metagenomic investigation proposed that Pelotomaculum and methanogens may interact with uncultivated organisms to degrade TA; however, many members of the community remained unaddressed because of past technological limitations. In further pursuit, this study employed state-of-the-art omics tools to generate draft genomes and transcriptomes for uncultivated organisms spanning 15 phyla and reports the first genomic insight into candidate phyla Atribacteria, Hydrogenedentes and Marinimicrobia in methanogenic environments. Metabolic reconstruction revealed that these organisms perform fermentative, syntrophic and acetogenic catabolism facilitated by energy conservation revolving around H-2 metabolism. Several of these organisms could degrade TA catabolism by-products (acetate, butyrate and H-2) and syntrophically support Pelotomaculum. Other taxa could scavenge anabolic products (protein and lipids) presumably derived from detrital biomass produced by the TA-degrading community. The protein scavengers expressed complementary metabolic pathways indicating syntrophic and fermentative step-wise protein degradation through amino acids, branched-chain fatty acids and propionate. Thus, the uncultivated organisms may interact to form an intricate syntrophy-supported food web with Pelotomaculum and methanogens to metabolize catabolic by-products and detritus, whereby facilitating holistic TA mineralization to CO2 and CH4.

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