• Login
    View Item 
    •   MINDS@UW Home
    • MINDS@UW Milwaukee
    • UW Milwaukee Electronic Theses and Dissertations
    • View Item
    •   MINDS@UW Home
    • MINDS@UW Milwaukee
    • UW Milwaukee Electronic Theses and Dissertations
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Quorum Sensing in Vibrios and Cross-Species Activation of Bioluminescence Lux Genes by Vibrio Harveyi LuxR in an Arabinose-Inducible Escherichia Coli Expression System

    Thumbnail
    File(s)
    Main File (2.628Mb)
    Date
    2013-05-01
    Author
    Wannamaker, Anne Marie
    Department
    Biological Sciences
    Advisor(s)
    Charles F. Wimpee
    Metadata
    Show full item record
    Abstract
    Bacterial bioluminescence is observed in over twenty known species, primarily in the family Vibrionaceae. However, only Vibrio fischeri and Vibrio harveyi bioluminescence expression mechanisms are well studied. In V. harveyi, expression of the lux operon is activated by the transcription factor LuxR (LuxRVH), resulting in bioluminescence. Homologs of LuxRVH in other Vibrio species have been shown to regulate transcription of a variety of genes. Three parallel quorum sensing pathways co-regulate the expression of LuxRVH. The first objective was to assess possible quorum sensing regulation of lux operon expression in V. cholerae, V. chagasii, V. orientalis, and V. vulnificus using V. harveyi as the control. Secondly, cross-species induction of bioluminescence by LuxRVH was tested on the aforementioned Vibrio lux operons using an Escherichia coli dual vector expression system. This was accomplished by first generating a plasmid with the V. harveyi luxR gene (luxRVH) driven by an arabinose promoter. Secondly, individual E. coli systems had one of the five Vibrio species-specific lux operons cloned on a separate plasmid. Luminescence was assayed qualitatively on plates, and quantitatively using a luminometer. Relative light per cell was calculated by dividing measured light by OD600. Relative light assays showed quorum sensing regulation of the lux operon in all five Vibrio species. Quantitative V. harveyi lux operon expression assays in the E. coli dual vector systems showed significant increase in light production in samples provided with arabinose. This demonstrated that induction of luxRVH by arabinose resulted in upregulation of lux genes. The level of LuxRVH activation of other Vibrio lux operons reflects the distance of evolutionary relationships to V. harveyi. The most induction was seen with the V. vulnificus lux operon followed by V. orientalis, V. chagasii, and finally V. cholerae. This implies conservation of the lux operon regulatory mechanism between closely related species and suggests that the studied Vibrios utilize LuxRVH-type transcription factors. The known LuxRVH homologs, SmcR (V. vulnificus) and HapR (V. cholerae) were suspected lux activators. In addition, other LuxRVH-type regulators are now implicated in the other Vibrio species. Furthermore, mechanistic conservation of these transcription factors implies regulation by V. harveyi-type quorum sensing.
    Subject
    Bioluminescence
    Lux Operon
    Luxr Homolog
    Quorum Sensing
    Transcriptional Activation
    Vibrio Harveyi
    Permanent Link
    http://digital.library.wisc.edu/1793/91639
    Type
    thesis
    Part of
    • UW Milwaukee Electronic Theses and Dissertations

    Contact Us | Send Feedback
     

     

    Browse

    All of MINDS@UWCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsThis CollectionBy Issue DateAuthorsTitlesSubjects

    My Account

    Login

    Contact Us | Send Feedback