Difference between revisions of "Part:BBa K1976001"

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                                 <p>The <i>λ</i>‑integrase, originally derived from the <i>λ</i>‑phage, catalyzes the recombination of the phage genome with the chromosomal genome of its host in combination with several assisting proteins. Therefore, two attachment sites are necessary: one located on the bacterial genome (<i>attB</i>) and the other located on the <i>λ</i>‑genome (<i>attP</i>), which also contains several binding sites for regulatory proteins. The attachment sites contain homologous recognition sequences, called BOB'&nbsp;region (<i>attB</i>) and COC'&nbsp;region (<i>attP</i>). These regions can be connected by the <i>λ</i>‑integrase and the bacterial <i>integration host factor</i> (IHF) via <i>Holliday junction</i>, forming an intasome, a DNA‑protein‑complex, producing hybrid attachment sites <i>attL</i> and <i>attR</i>. <br>
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                                 <p>The <i>λ</i>‑integrase, originally derived from the <i>λ</i>‑phage, catalyzes the recombination of the phage genome with the chromosomal genome of its host in combination with several assisting proteins. Therefore, two attachment sites are necessary: one located on the bacterial genome (<i>attB</i>) and the other located on the <i>λ</i>‑genome (<i>attP</i>), which also contains several binding sites for regulatory proteins. <br>
 
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             <p>The attachment sites contain homologous recognition sequences, called BOB'&nbsp;region (<i>attB</i>) and COC'&nbsp;region (<i>attP</i>). These regions can be connected by the <i>λ</i>‑integrase and the bacterial <i>integration host factor</i> (IHF) via <i>Holliday junction</i>, forming an intasome, a DNA‑protein‑complex, producing hybrid attachment sites <i>attL</i> and <i>attR</i>.</p> <br>
 
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                 <img src="https://static.igem.org/mediawiki/parts/0/0a/T--TU_Darmstadt--attPrecombination.png" style="width:50%">
 
                 <img src="https://static.igem.org/mediawiki/parts/0/0a/T--TU_Darmstadt--attPrecombination.png" style="width:50%">
                 <p align="center"><b>Figure 2:</b> The mechanism of &lambda;-integrase mediated <i>attP/attB</i>-recombination</p>
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                 <p align="center"><b>Figure 2:</b>&lambda;-integrase mediated <i>attP/attB</i>-recombination via <i>Holliday junctions</i></p> <br>
 
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Revision as of 11:04, 27 October 2016

λ-Integrase

The λ‑integrase, originally derived from the λ‑phage, catalyzes the recombination of the phage genome with the chromosomal genome of its host in combination with several assisting proteins. Therefore, two attachment sites are necessary: one located on the bacterial genome (attB) and the other located on the λ‑genome (attP), which also contains several binding sites for regulatory proteins.

λ-Integrase interacting with DNA

Figure 1: Crystal structure of the λ-Integrase in interaction with DNA. Created with VMD (Visual Molecular Dynamics).PDB entry, Biswas, T. et al. 2005

Recombination Process

The attachment sites contain homologous recognition sequences, called BOB' region (attB) and COC' region (attP). These regions can be connected by the λ‑integrase and the bacterial integration host factor (IHF) via Holliday junction, forming an intasome, a DNA‑protein‑complex, producing hybrid attachment sites attL and attR.


Figure 2:λ-integrase mediated attP/attB-recombination via Holliday junctions


Figure 3:

Usage and Biology

The λ-Integrase can be used for specific genomic integration of a variable gene of interest (GOI) via attP/attB recombination. For Integration of a certain GOI it has to be cloned into a vector carrying the λ-attP-site. The cloned plasmid together with the presented Part must be transformed into a λ-negative E. Coli-Strain with attB-site. The presented λ-Integrase is specific for the λ-attP-site used in BBa_K1976000.

Characterisation

Figure 4: SDS-Page after expression of λ-integrase gene. The gel band of λ-integrase is highlighted by the red circle.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


uniprotP03700