Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/8551
Title: ArgP protein of Escherichia coli: roles in osmoregulation, gene regulation and inter-relationship with LysG of Corynebacterium glutamicum
Researcher: Marbaniang, Carmelita N
Guide(s): Gowrishankar J
Keywords: Glutamate
LysR type of transcriptional regulator
Osmoregulation
Lysine repression
Nucleoid associated protein
Upload Date: 6-May-2013
University: Manipal University
Completed Date: 26/02/2013
Abstract: The ArgP protein of Escherichia coli had previously been described variously by different investigators as an inhibitor of oriC-initiated DNA replication, a nucleoid-associated protein and as a transcriptional regulator of genes involved in DNA replication (dnaA, nrdA), osmoregulation and amino acid metabolism (argO, dapB, gdhA and#61531;the last in Klebsiella pneumoniaeand#61533;). In the studies reported in this thesis, promoter-lac fusions were examined in argP+, and#61508;argP and dominant argP (argPd) mutations bearing strains to identify additional ArgP-regulated genes. The genes gdhA, lysP, lysC, lysA, dapD, and asd were newly identified as ArgP-regulated. All were repressed upon Lysine (Lys) supplementation, and in vitro studies demonstrated that ArgP binds to the regulatory regions in a Lys-sensitive manner ( in contrast to the behaviour at argO, where ArgP binding is Lys-insensitive). Unlike previous reports, neither dnaA nor nrdA was ArgP-regulated in vivo, although their regulatory regions did exhibit non-canonical low-affinity binding to ArgP in vitro. ArgP-argO of E. coli and LysG-lysE of Corynebacterium glutamicum are orthologous regulator-target gene pairs. While LysE is an exporter of both arginine (Arg) and Lys whose expression is induced by Arg, Lys, or histidine (His), ArgO exports Arg alone and its expression is activated by Arg but not Lys or His. In studies reported in this thesis, reconstitution of LysG activation of lysE in E. coli was achieved. Neither ArgP nor LysG could regulate expression of the non-cognate targets, but the ArgPd variants -P274S, -S94L -P108S activated lysE expression in E. coli. The activating effects of LysG and ArgPd on lysE were mutually extinguished when both proteins were co-expressed in Arg- or His-supplemented cultures. Compared to native ArgP, these ArgPds exhibited higher affinity of binding to lysE and less DNA bending at both argO and lysE.
Pagination: 210p.
URI: http://hdl.handle.net/10603/8551
Appears in Departments:Centre for DNA Fingerprinting and Diagnostics, Hyderabad

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03_abstract.pdf20.7 kBAdobe PDFView/Open
04_declaration.pdf49.1 kBAdobe PDFView/Open
05_acknowledgement.pdf70.76 kBAdobe PDFView/Open
06_contents.pdf176.24 kBAdobe PDFView/Open
07_list_of_tables.pdf91.85 kBAdobe PDFView/Open
08_list_of_figures.pdf78.57 kBAdobe PDFView/Open
09_abbreviations.pdf64.03 kBAdobe PDFView/Open
10_chapter1.pdf1.59 MBAdobe PDFView/Open
11_chapter2.pdf405.71 kBAdobe PDFView/Open
12_chapter3-7.pdf4.28 MBAdobe PDFView/Open
13_conclusion.pdf159.85 kBAdobe PDFView/Open
14_summary.pdf195.85 kBAdobe PDFView/Open
15_bibliography.pdf265.58 kBAdobe PDFView/Open


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