Difference between revisions of "Part:BBa K2668020"

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<p>The Sirius part (BBa_K2668020) correspond to a CBM3a and mRFP1 sequences fused by an endogenous C terminal linker. IDT performed the DNA synthesis and delivered the part as gBlock.  The construct was cloned by infusion into the pSB1C3 plasmid and then transformed into E. coli Dh5-alpha strain. Figure 1 shows the restriction map of the resulting clones.</p>
 
<p>The Sirius part (BBa_K2668020) correspond to a CBM3a and mRFP1 sequences fused by an endogenous C terminal linker. IDT performed the DNA synthesis and delivered the part as gBlock.  The construct was cloned by infusion into the pSB1C3 plasmid and then transformed into E. coli Dh5-alpha strain. Figure 1 shows the restriction map of the resulting clones.</p>
  
<figure class="figure"  style="text-align:center;"><img style="width : 70%; heigth = auto;" src="" alt="An awesome Agarose gel"><figcaption class="figure-caption"><strong>Figure 1:</strong> Figure 1: Analyses of pSB1C3_ CBM3a and mRFP1 length and restriction map. </figcaption></figure>
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<img style="width : 70%; heigth = auto;" src="" alt="An awesome Agarose gel"><br/><strong>Figure 1:</strong> Figure 1: Analyses of pSB1C3_ CBM3a and mRFP1 length and restriction map.
 
<h2>Characterisation</h2>
 
<h2>Characterisation</h2>
 
<h3>1. Production of Sirius</h3>
 
<h3>1. Production of Sirius</h3>

Revision as of 19:37, 9 October 2018


Sirius: CBM3a - mRFP1 fusion

Introduction

Sirius (BBa_K2668020) is a fusion protein between CBM3a and mRFP1. By fusing CBM3a to a fluorescent moiety, this part allowed us to investigate the binding capability of CBM3a platform to cellulose.

Construction

The Sirius part (BBa_K2668020) correspond to a CBM3a and mRFP1 sequences fused by an endogenous C terminal linker. IDT performed the DNA synthesis and delivered the part as gBlock. The construct was cloned by infusion into the pSB1C3 plasmid and then transformed into E. coli Dh5-alpha strain. Figure 1 shows the restriction map of the resulting clones.

<img style="width : 70%; heigth = auto;" src="" alt="An awesome Agarose gel">
Figure 1: Figure 1: Analyses of pSB1C3_ CBM3a and mRFP1 length and restriction map.

Characterisation

1. Production of Sirius

The part BBa_K2668020 was cloned into the pET28 expression vector using In-Fusion Cloning Kit. The resulting construct was transformed into E. coli strain BL21 and expression of the recombinant protein was induced using IPTG. The His-tagged protein was then purified on IMAC resin charged with cobalt. Results are shown on figure 2. A large amount of protein at the expected size for Sirius (52 kDa, lane CFE) was found predominant in elution samples (E1/40 and E1/100). The degree of purity of full length Sirius was about 72%. In addition to the full length protein, several extra bands that likely correspond to proteolysis products were observed.


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
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1272
    Illegal AgeI site found at 1384
  • 1000
    COMPATIBLE WITH RFC[1000]