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008 090602s2008 th uu|m rtt 0| a1eng d
035 _a.b12057381
099 9 _aAIT Diss. no.EV-08-10
100 0 _aWorawan Kitphati
245 1 0 _aPhysiological study of Ferric Uptake Regulator (FUR) gene in agrobacterium tumefaciens
260 _aPathum Thani, Thailand :
_bAsian Institute of Technology,
_c2008
300 _a136 p. :
_bill.
490 1 _aDissertation ;
_vno. EV-08-10
500 _aA dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Environmental Engineering and Management Inter-University Program on Environmen tal Toxicology, Technology and Management
502 _aThesis (Ph.D.) - Asian Institute of Technology - Chulabhorn Research Institute - Mahidol University, 2008
520 _aIron is an essential metal for bacterial survival due to the fact that it is a required cofactor in a large number of iron-containing enzymes and proteins. However, when present in excess it can be toxic due to its ability to induce the generation of highly deleterious free radicals via the Fenton reaction. Therefore, intracellular iron concentrations need to be carefully adjusted by controlling iron transport, storage and consumption. In many bacteria, this regulation is mediated by the ferric uptake regulator (Fur) protein. Fur is a 17 KDa DNA binding protein which represses the transcription of many iron-responsive genes in Escherichia coli and other bacteria. Fur regulates not only iron-regulated genes but also genes involved in; metal homeostasis, the oxidative stress response and virulence. Agrobacterium tumefaciens is a soil-born plant pathogen that causes crown gall tumor in many dicotyledonous plants. The A. tumefaciens genome encodes 3 fur homologues; fur, irr and zur. In order to determine the functional role of A.tumefaciens Fur, an A. tumefaciens fur mutant was constructed by insertional inactivation. The mutant construction was confirmed by Southern blot analysis. The phenotypes of this mutant relating to metal homeostasis and the oxidative stress response were investigated. Atypically, A.tumefaciens Fur did show alterations in the levels of siderophore biosynthesis. However, the A. tumefaciens fur mutant was more sensitive to an iron chelator, 2,2-dipyridyl, and more resistant to an iron-activated antibiotic, streptonigrin, than the wild type A. tumefaciens NTLâ‚„. This suggested that Fur has a role in regulating the intracellular iron concentration and that the A. tumefaciens fur mutant was iron-deficient. Apart from iron, A.tumefaciens Fur may also be involved in the regulation of divalent cation homeostasis. A. tumefaciens Fur was shown to playa role in the oxidative stress response. The A. tumefaciens fur mutant was hypersensitive to hydrogen peroxide and showed reduced catalase activity. Virulence assays showed that the A. tumefaciens fur mutant had a reduced ability to cause tumors on tobacco leaves compared to the wild type strain. The virulence deficiency of the A. tumefaciens fur mutant was proposed to be due, at least in part, to an impaired ability to cope with oxidative stress conditions caused primarily by a reduction in catalase levels
650 0 _aAgrobacterium tumefaciens
700 0 _aSkorn Mongkolsuk,
_eChairperson
700 0 _aPreeda Pakpian,
_eExamination Committee
700 0 _aSuvit Loprasert,
_eExamination committee
700 1 _aDubbs, James M.,
_eExamination committee
710 2 _aChulabhorn Research Institute,
_eScholarship donor
710 2 _aMahidol University,
_eScholarship donor
710 2 _aAsian Institute of Technology Fellowship,
_eScholarship donor
710 2 _aOffice of Higher Education Commission (OHEC), Thailand,
_eScholarship donor
810 2 _aAsian Institute of Technology.
_tDissertation ;
_vno. EV-08-10
856 _3Full-Text
_uhttp://203.159.5.9/ait-thesis/detail.php?q=B00534
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