Please use this identifier to cite or link to this item: https://doi.org/10.3390/pathogens5010009
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dc.titleApplication and optimization of relE as a negative selection marker for making definitive genetic constructs in uropathogenic escherichia coli
dc.contributor.authorKhetrapal, V
dc.contributor.authorMehershahi, K.S
dc.contributor.authorChen, S
dc.contributor.authorChen, S.L
dc.date.accessioned2020-09-02T07:01:16Z
dc.date.available2020-09-02T07:01:16Z
dc.date.issued2016
dc.identifier.citationKhetrapal, V, Mehershahi, K.S, Chen, S, Chen, S.L (2016). Application and optimization of relE as a negative selection marker for making definitive genetic constructs in uropathogenic escherichia coli. Pathogens 5 (1) : 1-6. ScholarBank@NUS Repository. https://doi.org/10.3390/pathogens5010009
dc.identifier.issn20760817
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/174032
dc.description.abstractStudies of Uropathogenic Escherichia coli (UPEC) pathogenesis have relied heavily on genetic manipulation to understand virulence factors. We applied a recently reported positive-negative selection system to create a series of unmarked, scarless FimH mutants that show identical phenotypes to previously reported marked FimH mutants; these are now improved versions useful for definitive assignment of phenotypes to FimH mutations. We also increased the efficiency of this system by designing new primer sites, which should further improve the efficiency and convenience of using negative selection in UTI89, other UPEC, and other Enterobacteriaceae. © 2016 by the authors; licensee MDPI, Basel, Switzerland.
dc.sourceUnpaywall 20200831
dc.subjectvirulence factor
dc.subjectArticle
dc.subjectbacterial strain
dc.subjectgene construct
dc.subjectgene mutation
dc.subjectgenetic organization
dc.subjecthemagglutination
dc.subjectnonhuman
dc.subjectphenotype
dc.subjectplasmid
dc.subjectpolymerase chain reaction
dc.subjectsequence analysis
dc.subjecturopathogenic Escherichia coli
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.description.doi10.3390/pathogens5010009
dc.description.sourcetitlePathogens
dc.description.volume5
dc.description.issue1
dc.description.page1-6
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