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- W2364383243 abstract "Objective To express the Hp1501 protein of Helicobacter pylori NCTC11637 strain in prokaryotic cells and purify the expressed product.Methods The Hp1501a sequence in encoding region of Hp1501 gene of H.pylori NCTC11637 strain was amplified by PCR and cloned into vector pQE30.The constructed recombinant plasmid pQE30-Hp1501a was transformed to E.coli XL1-blue and induced with IPTG,and the expressed recombinant protein was analyzed for form then purified by Ni-NTAHis column chromatography.Results Restriction analysis proved that recombinant plasmid pQE30-Hp1501a was constructed correctly.Sequencing result showed correct sequence of inserted gene.The expressed recombinant protein,with a relative molecular mass of about 37 000,contained about 21% of total somatic protein,mainly existed in a form of inclusion body,and showed specific binding to rabbit anti-His monoclonal antibody.After purification,the recombinant protein reached a purity of 91%.Conclusion The Hp1501 protein of H.pylori NCTC11637 strain was successfully expressed in prokaryotic cells and purified,which laid a foundation of study on biological function of H.pylori outer membrane protein and development of vaccine." @default.
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- W2364383243 date "2011-01-01" @default.
- W2364383243 modified "2023-09-24" @default.
- W2364383243 title "Prokaryotic Expression and Purification of Hp1501 Protein of Helicobacter pylori NCTC11637 Strain" @default.
- W2364383243 hasPublicationYear "2011" @default.
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