Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0111962
DC FieldValue
dc.titleCharacterization of the YdeO regulon in Escherichia coli
dc.contributor.authorYamanaka Y.
dc.contributor.authorOshima T.
dc.contributor.authorIshihama A.
dc.contributor.authorYamamoto K.
dc.date.accessioned2019-11-07T05:05:12Z
dc.date.available2019-11-07T05:05:12Z
dc.date.issued2014
dc.identifier.citationYamanaka Y., Oshima T., Ishihama A., Yamamoto K. (2014). Characterization of the YdeO regulon in Escherichia coli. PLoS ONE 9 (11) : e111962. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0111962
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161760
dc.description.abstractEnterobacteria are able to survive under stressful conditions within animals, such as acidic conditions in the stomach, bile salts during transfer to the intestine and anaerobic conditions within the intestine. The glutamate-dependent (GAD) system plays a major role in acid resistance in Escherichia coli, and expression of the GAD system is controlled by the regulatory cascade consisting of EvAS > YdeO> GadE. To understand the YdeO regulon in vivo, we used ChIP-chip to interrogate the E. coli genome for candidate YdeO binding sites. All of the seven operons identified by ChIP-chip as being potentially regulated by YdeO were confirmed as being under the direct control of YdeO using RT-qPCR, EMSA, DNaseI-footprinting and reporter assays. Within this YdeO regulon, we identified four stress-response transcription factors, DctR, NhaR, GadE, and GadW and enzymes for anaerobic respiration. Both GadE and GadW are involved in regulation of the GAD system and NhaR is an activator for the sodium/proton antiporter gene. In conjunction with co-transcribed Slp, DctR is involved in protection against metabolic endoproducts under acidic conditions. Taken all together, we suggest that YdeO is a key regulator of E. coli survival in both acidic and anaerobic conditions. © 2014 Yamanaka et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectantiporter
dc.subjectbacterial protein
dc.subjecttranscription factor
dc.subjecttranscription factor DctR
dc.subjecttranscription factor GadE
dc.subjecttranscription factor GadW
dc.subjecttranscription factor NhaR
dc.subjectunclassified drug
dc.subjectEscherichia coli protein
dc.subjectglutamic acid
dc.subjecttranscription factor
dc.subjectYdeO protein, E coli
dc.subjectanaerobic respiration
dc.subjectArticle
dc.subjectbacterial gene
dc.subjectbacterial genome
dc.subjectbacterial metabolism
dc.subjectbinding site
dc.subjectbreathing
dc.subjectcellular stress response
dc.subjectchromatin immunoprecipitation
dc.subjectDNA footprinting
dc.subjectEscherichia coli
dc.subjectgel mobility shift assay
dc.subjectgene function
dc.subjectgene identification
dc.subjectgenetic regulation
dc.subjectin vivo study
dc.subjectluciferase assay
dc.subjectmetabolic regulation
dc.subjectnonhuman
dc.subjectoperon
dc.subjectquantitative analysis
dc.subjectregulon
dc.subjectreverse transcription polymerase chain reaction
dc.subjectYdeO gene
dc.subjectanaerobic growth
dc.subjectEscherichia coli
dc.subjectgene expression profiling
dc.subjectgene expression regulation
dc.subjectgenetics
dc.subjectmetabolism
dc.subjectoperon
dc.subjectphysiological stress
dc.subjectphysiology
dc.subjectEscherichia coli
dc.subjectAnaerobiosis
dc.subjectBinding Sites
dc.subjectEscherichia coli
dc.subjectEscherichia coli Proteins
dc.subjectGene Expression Profiling
dc.subjectGene Expression Regulation, Bacterial
dc.subjectGlutamic Acid
dc.subjectOperon
dc.subjectStress, Physiological
dc.subjectTranscription Factors
dc.typeArticle
dc.contributor.departmentMECHANOBIOLOGY INSTITUTE
dc.description.doi10.1371/journal.pone.0111962
dc.description.sourcetitlePLoS ONE
dc.description.volume9
dc.description.issue11
dc.description.pagee111962
dc.published.statePublished
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