Chromosomal sequencing using a PCR-based biotin-capture method allowed isolation of the complete gene for the outer membrane protein A of Klebsiella pneumoniae
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Nguyen, TN
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机构:Kungliga Tekn Hgsk, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
Nguyen, TN
Samuelson, P
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机构:Kungliga Tekn Hgsk, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
Samuelson, P
Sterky, F
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机构:Kungliga Tekn Hgsk, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
Sterky, F
Merle-Poitte, C
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机构:Kungliga Tekn Hgsk, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
Merle-Poitte, C
Robert, A
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机构:Kungliga Tekn Hgsk, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
Robert, A
Baussant, T
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机构:Kungliga Tekn Hgsk, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
Baussant, T
Haeuw, JF
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机构:Kungliga Tekn Hgsk, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
Haeuw, JF
Uhlén, M
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机构:Kungliga Tekn Hgsk, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
Uhlén, M
Binz, H
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机构:Kungliga Tekn Hgsk, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
Binz, H
Ståhl, S
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机构:Kungliga Tekn Hgsk, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
Ståhl, S
机构:
[1] Kungliga Tekn Hgsk, Dept Biochem & Biotechnol, S-10044 Stockholm, Sweden
[2] Ctr Immunol Pierre Fabre, F-74164 St Julien En Genevois, France
By employing a novel biotin-and PCR-assisted capture method, which allows determination of unknown sequences on chromosomal DNA. the gene for the outer membrane protein A (OmpA) of Klebsiella pneumoniae has been isolated and sequenced to completion. The method involves linear amplification of DNA from a biotinylated primer annealing to a region with known sequence. After capture of the amplified single-stranded DNA on to paramagnetic beads, unspecifically annealing primers, i.e. arbitrary primers, were used to generate fragments with only partly determined nt sequences. The homology of the sequenced gene to ompAs of related bacteria is discussed. The ompA gene was assembled for intracellular expression in Escherichia coli, and two different fusion proteins were produced and recovered with good yields. The importance of the novel chromosomal sequencing method for gene isolation in general and the potential use of the OmpA fusion proteins are discussed. (C) 1998 Elsevier Science B.V.