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dc.contributor.authorNishiyama, Masayoshien
dc.contributor.authorSowa, Yoshiyukien
dc.contributor.authorKimura, Yoshifumien
dc.contributor.authorHomma, Michioen
dc.contributor.authorIshijima, Akihikoen
dc.contributor.authorTerazima, Masahideen
dc.contributor.alternative西山, 雅祥ja
dc.date.accessioned2015-08-07T06:33:50Z-
dc.date.available2015-08-07T06:33:50Z-
dc.date.issued2013-02-15-
dc.identifier.issn0021-9193-
dc.identifier.urihttp://hdl.handle.net/2433/198999-
dc.description.abstractThe bacterial flagellar motor is a reversible rotary machine that rotates a left-handed helical filament, allowing bacteria to swim toward a more favorable environment. The direction of rotation reverses from counterclockwise (CCW) to clockwise (CW), and vice versa, in response to input from the chemotaxis signaling circuit. CW rotation is normally caused by binding of the phosphorylated response regulator CheY (CheY-P), and strains lacking CheY are typically locked in CCW rotation. The detailed mechanism of switching remains unresolved because it is technically difficult to regulate the level of CheY-P within the concentration range that produces flagellar reversals. Here, we demonstrate that high hydrostatic pressure can induce CW rotation even in the absence of CheY-P. The rotation of single flagellar motors in Escherichia coli cells with the cheY gene deleted was monitored at various pressures and temperatures. Application of >120 MPa pressure induced a reversal from CCW to CW at 20°C, although at that temperature, no motor rotated CW at ambient pressure (0.1 MPa). At lower temperatures, pressure-induced changes in direction were observed at pressures of <120 MPa. CW rotation increased with pressure in a sigmoidal fashion, as it does in response to increasing concentrations of CheY-P. Application of pressure generally promotes the formation of clusters of ordered water molecules on the surfaces of proteins. It is possible that hydration of the switch complex at high pressure induces structural changes similar to those caused by the binding of CheY-P.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Society for Microbiologyen
dc.rightsCopyright © American Society for Microbiology, J. Bacteriol. April 2013 vol.195 no.8 1809-1814, doi: 10.1128/JB.02139-12.en
dc.subject.meshBacterial Proteins/geneticsen
dc.subject.meshBacterial Proteins/metabolismen
dc.subject.meshBiomechanical Phenomenaen
dc.subject.meshEscherichia coli/geneticsen
dc.subject.meshEscherichia coli/physiologyen
dc.subject.meshFlagella/physiologyen
dc.subject.meshGene Expression Regulation, Bacterial/physiologyen
dc.subject.meshHydrostatic Pressureen
dc.subject.meshMembrane Proteins/geneticsen
dc.subject.meshMembrane Proteins/metabolismen
dc.subject.meshMolecular Motor Proteins/physiologyen
dc.subject.meshMovement/physiologyen
dc.subject.meshProtein Bindingen
dc.subject.meshRotationen
dc.subject.meshTemperatureen
dc.subject.meshThermodynamicsen
dc.titleHigh hydrostatic pressure induces counterclockwise to clockwise reversals of the Escherichia coli flagellar motor.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA0069403X-
dc.identifier.jtitleJournal of bacteriologyen
dc.identifier.volume195-
dc.identifier.issue8-
dc.identifier.spage1809-
dc.identifier.epage1814-
dc.relation.doi10.1128/JB.02139-12-
dc.textversionpublisher-
dc.identifier.pmid23417485-
dcterms.accessRightsopen access-
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