English  |  正體中文  |  简体中文  |  Items with full text/Total items : 90074/105197 (86%)
Visitors : 7161374      Online Users : 106
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version

    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/2506

    Title: Functionl study of flhA and flhB genes in Xanthomonas campestris pv.campestris
    Authors: Yu-Wei leu
    Contributors: Department of Biotechnology
    Keywords: Yu-Wei leu;Rouh-Mei Hu;flhA and flhB
    Date: 2008
    Issue Date: 2009-11-06 14:11:12 (UTC+8)
    Publisher: Asia University
    Abstract: Xanthomonas campestris pv. campestris ( Xcc ) is a Gram negative, rod-shaped bacterium, and is a causative agent of black rot disease in cruciferous plants. According to previously reports, bacterial flagella and the type III secretion systems (TTSS) are highly related. The TTSS is essential for the virulence in many pathogens, including Xcc. Based on sequence homology, our search in Xcc revealed that more than 40 genes might be involved in the flagellar biogenesis. Six genes, rpoN, fleQ, fliA, flgM, fleN and flhF, have been demonstrated in our laboratory to be involved in the regulation of expression of many flagellar genes. In this work, we report the function of FlhA and FlhB which are homologs of TTSS proteins InvA and SpaS reported to be involved in the exportation of flagellar structure in Salmonlla. Xcc flhA and flhB mutants were obtained by insertional mutagenesis and were used for phenotypical assays. The flhA and flhB mutants are virulent, but immotile. Both mutants expressed a normal quantity of FleQ and RpoN protein. The expression of FliA protein was slightly decreased in an flhA mutant but not in an flhB mutant. Both mutants cannot synthesis the major flagellin protein FliC. Induction of plasmid-born wild-type flhA or flhB genes can successfully complement the motility defect, and restore the biosynthesis of FliC protein in flhA and flhB mutants, respectively. The promoter of fliC gene was transcribed by RNA polymerases containing an alternative sigma factor encoded by fliA gene. The FlgM protein is an anti-sigma factor acts against FliA. A mature flagellar TTSS expels FlgM from the cytoplasm and recover the function of FliA. As FlhA and FlhB are essential components of flagellar TTSS, the expression of fliC in flhA and flhB mutants might be blocked by an accumulation of cytoplasmic FlgM protein.

    The second part of this work is to use a yeast two-hybrid system to detect the protein-protein interaction between RpoN, FleQ, FleN, FlhF, FlgM, FliA and NtrC. The results suggested that RpoN2 and FlhF; RpoN2 and FleQ; RpoN2 and NtrC can
    interact with each other.
    Appears in Collections:[生物科技學系] 博碩士論文

    Files in This Item:

    File Description SizeFormat
    2506.doc25KbMicrosoft Word124View/Open

    All items in ASIAIR are protected by copyright, with all rights reserved.

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback