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dc.contributor.authorBooth, James
dc.contributor.authorŠpírek, Mário
dc.contributor.authorLobie, Tekle Airgecho
dc.contributor.authorSkarstad, Kirsten Jane
dc.contributor.authorKrejci, Lumir
dc.contributor.authorBjørås, Magnar
dc.date.accessioned2021-03-10T11:55:54Z
dc.date.available2021-03-10T11:55:54Z
dc.date.created2020-12-17T19:02:03Z
dc.date.issued2020
dc.identifier.citationScientific Reports. 2020, 10:19422 (1), 1-18.en_US
dc.identifier.issn2045-2322
dc.identifier.urihttps://hdl.handle.net/11250/2732609
dc.description.abstractExtracellular pH has been assumed to play little if any role in how bacteria respond to antibiotics and antibiotic resistance development. Here, we show that the intracellular pH of Escherichia coli equilibrates to the environmental pH following treatment with the DNA damaging antibiotic nalidixic acid. We demonstrate that this allows the environmental pH to influence the transcription of various DNA damage response genes and physiological processes such as filamentation. Using purified RecA and a known pH-sensitive mutant variant RecA K250R we show how pH can affect the biochemical activity of a protein central to control of the bacterial DNA damage response system. Finally, two different mutagenesis assays indicate that environmental pH affects antibiotic resistance development. Specifically, at environmental pH’s greater than six we find that mutagenesis plays a significant role in producing antibiotic resistant mutants. At pH’s less than or equal to 6 the genome appears more stable but extensive filamentation is observed, a phenomenon that has previously been linked to increased survival in the presence of macrophages.en_US
dc.language.isoengen_US
dc.publisherNature Researchen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleAntibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instabilityen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-18en_US
dc.source.volume10:19422en_US
dc.source.journalScientific Reportsen_US
dc.source.issue1en_US
dc.identifier.doi10.1038/s41598-020-76426-2
dc.identifier.cristin1861294
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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