| Literature DB >> 32483239 |
Shuying Geng1,2, Weizhang Fu3, Weifeng Chen4, Shulian Zheng5, Qi Gao6, Jing Wang1, Xiaohong Ge1.
Abstract
This study explored the effect of 70-mT magnetic field on wastewater treatment capacity for activated sludge in long-term laboratory-scale experiments. Metagenomic sequencing were conducted based on Illumina HiSeq 2000 platform after DNA extraction of the activated sludge. Then the effect of the magnetic field on the microbial unigene and metabolic pathways in activated sludge was investigated. As a result, higher pollutant removal was observed at 70 mT, with which the elimination of total nitrogen (TN) was the most effective. Functional genes annotated based on eggNOG database showed that unigenes related to information storage and processing were enhanced by the magnetic field. For CAZy classification, category such as glycosyl transferases was more abundant in the reactor with magnetic field, which has been shown to promote the entire energy supply pathway. Additionally, in the KEGG categories, unigenes related to signaling molecules and interaction were significantly inhibited. Through the enrichment analysis of the nitrogen metabolism pathway, the magnetic field inhibited anabolic nitrate reduction by significantly inhibiting enzymes such as [EC:1.7.7.2], [EC:1.7.7.1], [EC:3.5.5.1], [EC:1.4.1.2] and [EC:4.2.1.1], which are related to the improvement of the denitrification ability. This study can provide insight for future research on the response mechanism of activated sludge to magnetic fields.Entities:
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Year: 2020 PMID: 32483239 PMCID: PMC7264255 DOI: 10.1038/s41598-020-65795-3
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379
Figure 1Long-term treatment performance of wastewater with (M) and without (CK) the application of a magnetic field: (A) changes in COD concentration and removal rate; (B) changes in TN concentration and removal rate; (C) changes in TP concentration and removal rate; and (D) comparison of the pollution removal effect.
Figure 2Changes in ambient temperature during the experiment.
Assembly and sequencing statistics for the activated sludge samples.
| Parameter | CK | M |
|---|---|---|
| Raw reads | 104,261,932 | 72,952,276 |
| Raw bases | 15,743,551,732 | 11,015,793,676 |
| Clean reads | 94,231,934 | 65,438,191 |
| Clean bases | 14,098,350,576 | 9,791,938,998 |
| Minimum sequence length (bp) | 200 | 200 |
| Maximum sequence length (bp) | 669,717 | 739,536 |
| N50 length (bp) | 1,902 | 2,050 |
| Total sequences | 444,274 | 67,707 |
| Macronomic length (bp) | 532,318,741 | 530,334,523 |
| GC base count | 300,608,981 | 299,397,251 |
| Sequences of length > 1 kb | 119,179 | 116.148 |
Figure 3Distribution of the KEGG classification in the activated sludge macrogenome: (a) composition and abundance of six KEGG functional genes in the macrogenome of activated sludge; (b) content of KEGG level-1 functional genes in the macrogenome of activated sludge; and (c) the ratios of unigene contents in M to CK.
Figure 4Distribution and comparison of the eggNOG categories.
Figure 5Distribution differences among the CAZy classifications.
Statistical table for the abundance difference analysis.
| Group | KO | eggNOG | CAZy |
|---|---|---|---|
| CK-M | 3,368 | 24,055 | 62 |
Figure 6Common KEGG metabolic pathway.