Please use this identifier to cite or link to this item: https://doi.org/10.3389/fmicb.2017.01575
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dc.titleCoordination of chromosome segregation and cell division in Staphylococcus aureus
dc.contributor.authorBottomley, A.L
dc.contributor.authorLiew, A.T.F
dc.contributor.authorKusuma, K.D
dc.contributor.authorPeterson, E
dc.contributor.authorSeidel, L
dc.contributor.authorFoster, S.J
dc.contributor.authorHarry, E.J
dc.date.accessioned2020-10-23T04:40:52Z
dc.date.available2020-10-23T04:40:52Z
dc.date.issued2017
dc.identifier.citationBottomley, A.L, Liew, A.T.F, Kusuma, K.D, Peterson, E, Seidel, L, Foster, S.J, Harry, E.J (2017). Coordination of chromosome segregation and cell division in Staphylococcus aureus. Frontiers in Microbiology 8 (AUG) : 1575. ScholarBank@NUS Repository. https://doi.org/10.3389/fmicb.2017.01575
dc.identifier.issn1664302X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/179463
dc.description.abstractProductive bacterial cell division and survival of progeny requires tight coordination between chromosome segregation and cell division to ensure equal partitioning of DNA. Unlike rod-shaped bacteria that undergo division in one plane, the coccoid human pathogen Staphylococcus aureus divides in three successive orthogonal planes, which requires a different spatial control compared to rod-shaped cells. To gain a better understanding of how this coordination between chromosome segregation and cell division is regulated in S. aureus, we investigated proteins that associate with FtsZ and the divisome. We found that DnaK, a well-known chaperone, interacts with FtsZ, EzrA and DivIVA, and is required for DivIVA stability. Unlike in several rod shaped organisms, DivIVA in S. aureus associates with several components of the divisome, as well as the chromosome segregation protein, SMC. This data, combined with phenotypic analysis of mutants, suggests a novel role for S. aureus DivIVA in ensuring cell division and chromosome segregation are coordinated. @ 2017 Bottomley, Liew, Kusuma, Peterson, Seidel, Foster and Harry.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectFtsZ protein
dc.subjectprotein DnaK
dc.subjectArticle
dc.subjectBacillus subtilis
dc.subjectcell division
dc.subjectcell viability
dc.subjectchromosome segregation
dc.subjectcontrolled study
dc.subjectcytolysis
dc.subjectelectroporation
dc.subjectfluorescence microscopy
dc.subjectgrowth rate
dc.subjectimmunoblotting
dc.subjectliquid chromatography-mass spectrometry
dc.subjectmicroscopy
dc.subjectnonhuman
dc.subjectphenotype
dc.subjectpolyacrylamide gel electrophoresis
dc.subjectpolymerase chain reaction
dc.subjectprotein purification
dc.subjectStaphylococcus aureus
dc.subjectWestern blotting
dc.typeArticle
dc.contributor.departmentMECHANOBIOLOGY INSTITUTE
dc.description.doi10.3389/fmicb.2017.01575
dc.description.sourcetitleFrontiers in Microbiology
dc.description.volume8
dc.description.issueAUG
dc.description.page1575
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