期刊
BIOTECHNOLOGY AND BIOENGINEERING
卷 118, 期 1, 页码 433-441出版社
WILEY
DOI: 10.1002/bit.27581
关键词
activated sludge; functional diversity; metagenomics; community genomics; microbial communities; partial nitritation anammox
资金
- Projekt DEAL
A metagenomic analysis revealed distinct abundance patterns of denitrification pathway genes and their association to microbial species between PNA and AS systems, suggesting niche separation exists. Taxonomic analysis based on the 16S rRNA gene did not detect notable variability in denitrifying community composition across samples. Targeted metagenomics can help determine denitrifying microbial composition at a fine-scale resolution, overcoming biases in quantitative polymerase chain reaction approaches.
The substantial presence of denitrifiers has already been reported in partial nitritation anammox (PNA) systems using the 16S ribosomal RNA (rRNA) gene, but little is known about the phylogenetic diversity based on denitrification pathway functional genes. Therefore, we performed a metagenomic analysis to determine the distribution of denitrification genes and the associated phylogeny in PNA systems and whether a niche separation between PNA and conventional activated sludge (AS) systems exists. The results revealed a distinct abundance pattern of denitrification pathway genes and their association to the microbial species between PNA and AS systems. In contrast, the taxonomic analysis, based on the 16S rRNA gene, did not detect notable variability in denitrifying community composition across samples. In general, narG and nosZa2 genes were dominant in all samples. While the potential for different stages of denitrification was redundant, variation in species composition and lack of the complete denitrification gene pool in each species appears to confer niche separation between PNA and AS systems. This study suggests that targeted metagenomics can help to determine the denitrifying microbial composition at a fine-scale resolution while overcoming current biases in quantitative polymerase chain reaction approaches due to a lack of appropriate primers.
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