Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

ABSTRACT: Studies of MBBR coupling GDMBR in treating decentralized domestic wastewater

PROVIDER: PRJNA1215698 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
	SRR32123967_1.fastq.gz	Fastqsanger.gz
	SRR32123967_2.fastq.gz	Fastqsanger.gz
	SRR32123968_1.fastq.gz	Fastqsanger.gz
	SRR32123968_2.fastq.gz	Fastqsanger.gz
	SRR32123969_1.fastq.gz	Fastqsanger.gz

Items per page:

1 - 5 of 20

Similar Datasets

biofilm metagenome

Project description:MBBR treating wastewater Targeted Locus

| PRJNA191904 | ENA

Project description:Long-term MBBR system treating real municipal wastewater

| PRJNA896724 | ENA

Project description:Microbial information of MBBR wastewater treatment, the application of Novel GAC-bioball engaged MBBR treating municipal wastewater

| PRJNA1260677 | ENA

sidestream wastewater samples

Project description:MBfR coupling anammox and n-DAMO microorganisms treating sidestream wastewater

| PRJNA635509 | ENA

Project description:Eco-friendly nitrogen removal from decentralized domestic wastewater using gravel-bed coupled with wood chip

| PRJNA1226409 | ENA

Project description:Pyrosequencing result of the microbial fuel cell for treating domestic wastewater

| PRJNA358453 | ENA

Project description:MiSeq result of the microbial nitrogen-removal cells (MNCs) treating domestic wastewater

| PRJNA384885 | ENA

Project description:Functional bacteria in domestic sewage treating

| PRJNA690678 | ENA

Monobromobimane labelling in early- and late-passage primary human mesemchymal stem cells subjected to 2 hour heat shock

Project description:Monobromobimane (mBBr) labelling: mBBr labelling was carried out either immediately prior to 42°C, two hour heat shock, or immediately following heat shock. Medium was removed from culture flasks and cells were washed using PBS. Cells were then labelled by incubation at 37°C with 6 mL of 400 µM mBBr (Sigma-Aldrich, #B4380) for 10 minutes. Following labeling, 6 ml of 2 mM L-glutathione reduced (GSH, SigmaAldrich, #G4251) in PBS was added to quench the mBBr reaction. The quenched mBBr solution was removed and cells were washed with PBS. Mass spectrometry (MS) sample preparation, analysis and data processing: Six 1.6 mm steel beads (Next Advance Inc.) were added to the cell pellet tube with 30 µL SL-DOC (1.1% (w/w) sodium dodecyl sulfate (Sigma), 0.3% (w/w) sodium deoxycholate (Sigma), 25 mM ammonium bicarbonate (AB, Fluka), in de-ionised (DI) water containing 0.1% (v/v) protease inhibitor cocktail (Sigma), and 0.1% (v/v) phosphotase inhibitor cocktail (Sigma). Cells were homogen

2021-06-15 | PXD025329 | Pride

DNA microarray analysis for HepG2 cells exposed to wastewater effluents

Project description:The transcriptome analysis by the human DNA microarray was applied to evaluate the impacts of whole wastewater effluents from the membrane bioreactors (MBRs) and the activated sludge process (AS), on the biological processes of human hepatoma HepG2 cells. The three conventional bioassays (i.e., cytotoxicity tests and bioluminescence inhibition test) and chemical analysis of the domestic effluent standards were conducted in parallel since they are well-established methods with previous applications to wastewater. A significant variation of effluent quality was sdemonstrated among the tested effluents despite that all effluents met the 40 national effluent standards. The three conventional bioassays supported the result of the transcriptome analysis, indicating the comparable or even higher sensitivity of the new assay. The most superior effluent quality was found in the MBR operated at a relatively long sludge retention time (i.e., 40 days) and small membrane pore size (i.e., 0.03 M-NM-<m). In addition, functional analysis of the differentially expressed genes revealed that the effluents made various impacts on the cellular functions, suggesting the transcriptome analysis by DNA microarray as more comprehensive, rapid and sensitive tool to detect multiple impacts of the whole effluents. Moreover, the potential genetic markers were proposed to quantitatively evaluate the treatability of the wastewater effluents. In this study, we examined the gene expression alteration in human hepatoma cell line, HepG2 exposed to the raw wastewater, effluents from three types of membrane bioreactors (MBRs), and the activated sludge process. Wastewater DNA microarray with 8795 human genes. MQ water was used as control. For duplicate, two dishes were prepared for each sample and individually treated in parallel.

2013-03-29 | E-GEOD-45605 | biostudies-arrayexpress

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data