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Article: Extracellular DNA Promotes Efficient Extracellular Electron Transfer by Pyocyanin in Pseudomonas aeruginosa Biofilms

TitleExtracellular DNA Promotes Efficient Extracellular Electron Transfer by Pyocyanin in Pseudomonas aeruginosa Biofilms
Authors
Keywordsbiofilm
phenazine
extracellular electron transfer
Pseudomonas aeruginosa
pyocyanin
Issue Date2020
PublisherCell Press. The Journal's web site is located at http://www.elsevier.com/locate/cell
Citation
Cell, 2020, v. 182 n. 4, p. 919-932.E19 How to Cite?
AbstractRedox cycling of extracellular electron shuttles can enable the metabolic activity of subpopulations within multicellular bacterial biofilms that lack direct access to electron acceptors or donors. How these shuttles catalyze extracellular electron transfer (EET) within biofilms without being lost to the environment has been a long-standing question. Here, we show that phenazines mediate efficient EET through interactions with extracellular DNA (eDNA) in Pseudomonas aeruginosa biofilms. Retention of pyocyanin (PYO) and phenazine carboxamide in the biofilm matrix is facilitated by eDNA binding. In vitro, different phenazines can exchange electrons in the presence or absence of DNA and can participate directly in redox reactions through DNA. In vivo, biofilm eDNA can also support rapid electron transfer between redox active intercalators. Together, these results establish that PYO:eDNA interactions support an efficient redox cycle with rapid EET that is faster than the rate of PYO loss from the biofilm.
Persistent Identifierhttp://hdl.handle.net/10722/285273
ISSN
2023 Impact Factor: 45.5
2023 SCImago Journal Rankings: 24.342
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorSaunders, SH-
dc.contributor.authorTse, ECM-
dc.contributor.authorYates, MD-
dc.contributor.authorOtero, FJ-
dc.contributor.authorTrammell, SA-
dc.contributor.authorStemp, EDA-
dc.contributor.authorBarton, JK-
dc.contributor.authorTender, LM-
dc.contributor.authorNewman, DK-
dc.date.accessioned2020-08-18T03:51:54Z-
dc.date.available2020-08-18T03:51:54Z-
dc.date.issued2020-
dc.identifier.citationCell, 2020, v. 182 n. 4, p. 919-932.E19-
dc.identifier.issn0092-8674-
dc.identifier.urihttp://hdl.handle.net/10722/285273-
dc.description.abstractRedox cycling of extracellular electron shuttles can enable the metabolic activity of subpopulations within multicellular bacterial biofilms that lack direct access to electron acceptors or donors. How these shuttles catalyze extracellular electron transfer (EET) within biofilms without being lost to the environment has been a long-standing question. Here, we show that phenazines mediate efficient EET through interactions with extracellular DNA (eDNA) in Pseudomonas aeruginosa biofilms. Retention of pyocyanin (PYO) and phenazine carboxamide in the biofilm matrix is facilitated by eDNA binding. In vitro, different phenazines can exchange electrons in the presence or absence of DNA and can participate directly in redox reactions through DNA. In vivo, biofilm eDNA can also support rapid electron transfer between redox active intercalators. Together, these results establish that PYO:eDNA interactions support an efficient redox cycle with rapid EET that is faster than the rate of PYO loss from the biofilm.-
dc.languageeng-
dc.publisherCell Press. The Journal's web site is located at http://www.elsevier.com/locate/cell-
dc.relation.ispartofCell-
dc.subjectbiofilm-
dc.subjectphenazine-
dc.subjectextracellular electron transfer-
dc.subjectPseudomonas aeruginosa-
dc.subjectpyocyanin-
dc.titleExtracellular DNA Promotes Efficient Extracellular Electron Transfer by Pyocyanin in Pseudomonas aeruginosa Biofilms-
dc.typeArticle-
dc.identifier.emailTse, ECM: ecmtse@hku.hk-
dc.identifier.authorityTse, ECM=rp02452-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1016/j.cell.2020.07.006-
dc.identifier.pmid32763156-
dc.identifier.pmcidPMC7457544-
dc.identifier.scopuseid_2-s2.0-85089414524-
dc.identifier.hkuros312766-
dc.identifier.volume182-
dc.identifier.issue4-
dc.identifier.spage919-
dc.identifier.epage932.E19-
dc.identifier.isiWOS:000561488500013-
dc.publisher.placeUnited States-
dc.identifier.issnl0092-8674-

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