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      Cloning and Expression of Genes Encoding F107-C and K88-1NT Fimbrial Proteins of Enterotoxigenic Escherichia coli from Piglets.

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          Abstract

          We cloned two genes coding F107-C and K88-1NT fimbrial subunits from strains E. coli C and 1NT isolated from Thua Thien Hue province, Vietnam. The mature peptide of faeG gene from strain E. coli 1NT (called faeG-1NT) is 100 % similarity with faeG gene, while the CDS of fedA gene from strain C (called fedA-C) has a similarity of 97 % with the fedA gene. Expression of the faeG-1NT and fedA-C genes in E. coli BL21 Star™ (DE3) produced proteins of ~31 and 22 kDa, respectively. The effect of IPTG concentration on the K88-1NT and F107-C fimbriae production was investigated. The results showed that 0.5 mM IPTG is suitable for higher expression of K88-1NT subunit, while 0.75 mM IPTG strongly stimulated expression of F107-C subunit. The optimal induction time for expression was also examined. Generally, highest expression of K88-1NT subunit occurred after 6 h of induction, while that of F107-C subunit is after 14 h.

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          Author and article information

          Journal
          Indian J. Microbiol.
          Indian journal of microbiology
          Springer Nature America, Inc
          0046-8991
          0046-8991
          Dec 2013
          : 53
          : 4
          Affiliations
          [1 ] Institute of Resources, Environment and Biotechnology, Hue University, Hue, 47000 Vietnam.
          [2 ] College of Agriculture and Forestry, Hue University, Hue, 47000 Vietnam.
          Article
          386
          10.1007/s12088-013-0386-z
          3779301
          24426156
          c2244523-a8ef-4c08-8d51-6a17e8832234
          History

          K88-1NT,Fimbriae,F107-C,E. coli,faeG,fedA
          K88-1NT, Fimbriae, F107-C, E. coli, faeG, fedA

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