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Sökning: id:"swepub:oai:DiVA.org:oru-12889" > Expression of Helic...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004118naa a2200493 4500
001oai:DiVA.org:oru-12889
003SwePub
008110103s2010 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:121244701
024a https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-128892 URI
024a https://doi.org/10.1111/j.1523-5378.2010.00786.x2 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1212447012 URI
040 a (SwePub)orud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Kalbina, Irinau Örebro universitet,Akademin för naturvetenskap och teknik4 aut0 (Swepub:oru)ika
2451 0a Expression of Helicobacter pylori TonB Protein in Transgenic Arabidopsis thaliana :b toward production of vaccine antigens in plants
264 c 2010-09-07
264 1b John Wiley & Sons,c 2010
338 a electronic2 rdacarrier
500 a This is a pre-print article.
520 a Background: The aim of this study was to produce a recombinant version of the highly antigenic Helicobacter pylori TonB (iron-dependent siderophore transporter protein HP1341) in transgenic plants as a candidate oral vaccine antigen. Materials and Methods: Using Agrobacterium-mediated gene transfer, we introduced three different constructs of the tonB gene into the genome of the model plant Arabidopsis thaliana. We investigated transgene insertion by PCR, produced TonB antibodies for analysis of the production of the recombinant protein in plants, verified the identity of the protein produced by mass spectrometry analysis, and analyzed the number of genetic inserts in the plants by Southern blotting. Results: Three different constructs of the expression cassette (full-length tonB, tonB truncated in the 5' end removing the codons for a transmembrane helix, and the latter construct with codons for the endoplasmic reticulum SEKDEL retention signal added to the 3' end) were used to find the most effective way to express the TonB antigen. Production of TonB protein was detected in plants transformed with each of the constructs, confirmed by both Western blotting and mass spectrometry analysis. No considerable differences in protein expression from the three different constructs were observed. The protein concentration in the plants was at least 0.05% of the total soluble proteins. Conclusions: The Helicobacter pylori TonB protein can be produced in Arabidopsis thaliana plants in a form that is recognizable by rabbit anti-TonB antiserum. These TonB-expressing plants are highly suitable for animal studies of oral adminstration as a route for immunization against Helicobacter infections.
650 7a NATURVETENSKAPx Biologix Biokemi och molekylärbiologi0 (SwePub)106022 hsv//swe
650 7a NATURAL SCIENCESx Biological Sciencesx Biochemistry and Molecular Biology0 (SwePub)106022 hsv//eng
653 a edible vaccines
653 a Helicobacter pylori
653 a HP1341
653 a subunit vaccine
653 a TonB
653 a transgenic plants
653 a Biochemistry
653 a Biokemi
700a Engstrand, Larsu Karolinska Institutet4 aut
700a Andersson, Sörenu Örebro University Hospital, Örebro, Sweden; Dept Bacteriol, Swedish Inst Infect Dis Control SMI, Solna, Sweden4 aut0 (Swepub:oru)sean
700a Strid, Åkeu Örebro universitet,Akademin för naturvetenskap och teknik4 aut0 (Swepub:oru)aesd
710a Örebro universitetb Akademin för naturvetenskap och teknik4 org
773t Helicobacterd : John Wiley & Sonsg 15:5, s. 430-437q 15:5<430-437x 1083-4389x 1523-5378
856u https://oru.diva-portal.org/smash/get/diva2:383450/FULLTEXT01.pdfx primaryx Raw objecty fulltext:postprint
856u http://oru.diva-portal.org/smash/get/diva2:383450/FULLTEXT01
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-12889
8564 8u https://doi.org/10.1111/j.1523-5378.2010.00786.x
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:121244701

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