Fluorescent reporters for markerless genomic integration in Staphylococcus aureus

Nienke W.M. De Jong, Thijs Van Der Horst, Jos A.G. Van Strijp, Reindert Nijland

Research output: Contribution to journalArticleAcademicpeer-review

4 Citations (Scopus)

Abstract

We present integration vectors for Staphylococcus aureus encoding the fluorescent reporters mAmetrine, CFP, sGFP, YFP, mCherry and mKate. The expression is driven either from the sarA-P1 promoter or from any other promoter of choice. The reporter can be inserted markerless in the chromosome of a wide range of S. aureus strains. The integration site chosen does not disrupt any open reading frame, provides good expression, and has no detectable effect on the strains physiology. As an intermediate construct, we present a set of replicating plasmids containing the same fluorescent reporters. Also in these reporter plasmids the sarA-P1 promoter can be replaced by any other promoter of interest for expression studies. Cassettes from the replication plasmids can be readily swapped with the integration vector. With these constructs it becomes possible to monitor reporters of separate fluorescent wavelengths simultaneously.
LanguageEnglish
Article number43889
JournalScientific Reports
Volume7
DOIs
Publication statusPublished - 2017

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Staphylococcus aureus
Plasmids
Open Reading Frames
Chromosomes

Cite this

De Jong, Nienke W.M. ; Van Der Horst, Thijs ; Van Strijp, Jos A.G. ; Nijland, Reindert. / Fluorescent reporters for markerless genomic integration in Staphylococcus aureus. In: Scientific Reports. 2017 ; Vol. 7.
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Fluorescent reporters for markerless genomic integration in Staphylococcus aureus. / De Jong, Nienke W.M.; Van Der Horst, Thijs; Van Strijp, Jos A.G.; Nijland, Reindert.

In: Scientific Reports, Vol. 7, 43889, 2017.

Research output: Contribution to journalArticleAcademicpeer-review

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