Difference between revisions of "Part:BBa K3429002"
 
(One intermediate revision by one other user not shown)
Line 7: Line 7:
 
                 <tr>
 
                 <tr>
 
                     <td><b>Name</b></td>
 
                     <td><b>Name</b></td>
−
                     <td>TasA matrix protein</td>
+
                     <td>superfolder Green Fluorescent Protein (sfGFP)</td>
 
                 </tr>
 
                 </tr>
 
                 <tr>
 
                 <tr>
 
                     <td><b>Base pairs</b></td>
 
                     <td><b>Base pairs</b></td>
−
                     <td>786</td>
+
                     <td>714</td>
 
                 </tr>
 
                 </tr>
 
                 <tr>
 
                 <tr>
Line 23: Line 23:
 
             </table>
 
             </table>
  
−
The superfolder green fluorescent protein (sfGFP) is a, for B. subtilis codon-optimized, derivative of the GFP. Huang et al. was able to demonstrate its function as a reporter fused with the TasA protein. <sup> [1] </sup> We implement it as a reporter and experimental control for our TasA fusion proteins with the enzymes CotA, CuO and EreB.  
+
The superfolder green fluorescent protein (sfGFP) is a, for B. subtilis codon-optimized, derivative of the GFP. Huang et al. was able to demonstrate its function as a reporter fused with the TasA protein<sup>[1]</sup>.  We implement it as a reporter and experimental control for our TasA fusion proteins with the enzymes CotA, CuO and EreB.  
  
  

Latest revision as of 09:29, 26 October 2020


Superfolder Green Fluorescent Protein (sfGFP)

Profile

Name superfolder Green Fluorescent Protein (sfGFP)
Base pairs 714
Molecular weight 26.8 kDa
Origin Aequorea victoria, synthetic

The superfolder green fluorescent protein (sfGFP) is a, for B. subtilis codon-optimized, derivative of the GFP. Huang et al. was able to demonstrate its function as a reporter fused with the TasA protein[1]. We implement it as a reporter and experimental control for our TasA fusion proteins with the enzymes CotA, CuO and EreB.


References

[1] Huang, J., Liu, S., Zhang, C. et al., Programmable and printable Bacillus subtilis biofilms as engineered living materials. Nat Chem Biol 15, 34–41, (2019), https://doi.org/10.1038/s41589-018-0169-2



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]