4.3 Article

Low-temperature anaerobic digestion is associated with differential methanogenic protein expression

期刊

FEMS MICROBIOLOGY LETTERS
卷 362, 期 10, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/femsle/fnv059

关键词

anaerobic digestion; metaproteomics; microbial phylogenetic diversity; methanogenic community; low temperature

资金

  1. Science Foundation Ireland [RFP 08/RFP/EOB1343, 06/CP/E006]
  2. Welcome Trust [GR06281AIA]
  3. Science Foundation Ireland (SFI) [06/CP/E006] Funding Source: Science Foundation Ireland (SFI)

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Anaerobic digestion (AD) is an attractive wastewater treatment technology, leading to the generation of recoverable biofuel (methane). Most industrial AD applications, carry excessive heating costs, however, as AD reactors are commonly operated at mesophilic temperatures while handling waste streams discharged at ambient or cold temperatures. Consequently, low-temperature AD represents a cost-effective strategy for wastewater treatment. The comparative investigation of key microbial groups underpinning laboratory-scale AD bioreactors operated at 37, 15 and 7 degrees C was carried out. Community structure was monitored using 16S rRNA clone libraries, while abundance of the most prominent methanogens was investigated using qPCR. In addition, metaproteomics was employed to access the microbial functions carried out in situ. While d-Proteobacteria were prevalent at 37 degrees C, their abundance decreased dramatically at lower temperatures with inverse trends observed for Bacteroidetes and Firmicutes. Methanobacteriales and Methanosaeta were predominant at all temperatures investigated while Methanomicrobiales abundance increased at 15 degrees C compared to 37 and 7 degrees C. Changes in operating temperature resulted in the differential expression of proteins involved in methanogenesis, which was found to occur in all bioreactors, as corroborated by bioreactors' performance. This study demonstrated the value of employing a polyphasic approach to address microbial community dynamics and highlighted the functional redundancy of AD microbiomes.

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