Difference between revisions of "Part:BBa K1039000"

 
 
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<partinfo>BBa_K1039000 short</partinfo>
 
<partinfo>BBa_K1039000 short</partinfo>
  
 
The attP site is the phage attachment site for the phiC31 phage. The site is recognized by phiC31 integrase. The phiC31 integrase catalyzes a unidirectional strand exchange between a 39 bp attP site and a 34 bp attB site (Groth et al., 2000). The enzyme works by making a synapse between attP and attB, making double strand breaks producing a 2 bp sticky overhang, exchanging the strands, and re-ligating them in the recombinant configuration (attL and attR).   
 
The attP site is the phage attachment site for the phiC31 phage. The site is recognized by phiC31 integrase. The phiC31 integrase catalyzes a unidirectional strand exchange between a 39 bp attP site and a 34 bp attB site (Groth et al., 2000). The enzyme works by making a synapse between attP and attB, making double strand breaks producing a 2 bp sticky overhang, exchanging the strands, and re-ligating them in the recombinant configuration (attL and attR).   
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Reference: Amy C. Groth, Michele P. Calos, Phage Integrases: Biology and Applications, Journal of Molecular Biology, Volume 335, Issue 3, 16 January 2004, Pages 667-678, ISSN 0022-2836, http://dx.doi.org/10.1016/j.jmb.2003.09.082. Sequence and Features
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=Improvement and Characterization by Fudan_China 2017=
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*'''Group:''' Fudan_China 2017
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*'''Author:''' Haiyun Liu, Fudan University
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We improved this part and characterized the kinetic characterization and the orthogonality between the integrase and some other serine recombinase using this improved attP site ([[Part:BBa_K24600011|BBa_K2460011]]). For more information, go to [[Part:BBa_K1039012|phiC31 integrase]].
  
 
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Latest revision as of 03:07, 2 November 2017

attP site for phiC31 integrase

The attP site is the phage attachment site for the phiC31 phage. The site is recognized by phiC31 integrase. The phiC31 integrase catalyzes a unidirectional strand exchange between a 39 bp attP site and a 34 bp attB site (Groth et al., 2000). The enzyme works by making a synapse between attP and attB, making double strand breaks producing a 2 bp sticky overhang, exchanging the strands, and re-ligating them in the recombinant configuration (attL and attR).

Reference: Amy C. Groth, Michele P. Calos, Phage Integrases: Biology and Applications, Journal of Molecular Biology, Volume 335, Issue 3, 16 January 2004, Pages 667-678, ISSN 0022-2836, http://dx.doi.org/10.1016/j.jmb.2003.09.082. Sequence and Features

Improvement and Characterization by Fudan_China 2017

  • Group: Fudan_China 2017
  • Author: Haiyun Liu, Fudan University

We improved this part and characterized the kinetic characterization and the orthogonality between the integrase and some other serine recombinase using this improved attP site (BBa_K2460011). For more information, go to phiC31 integrase.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]