Difference between revisions of "Part:BBa K4361302"
 
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<li>G 474 > T, silent mutation</li>
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<li>T 529 > C, resulting in substitution F177L</li>
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<li>G 606 > T, silent mutation</li>
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<li>T 618 > A, silent mutation</li>
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<li>G 648 > T, resulting in substitution E216D</li>
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<li>T 681 > A, resulting in substitution E227D</li>
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<li>G 742 > A, resulting in substitution E248A</li>
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<li>A 745 > C, resulting in substitution K249Q</li>
 
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<span class='h3bb'>Sequence and Features</span>
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<span class='h3bb'><h3>Sequence and Features</h3></span>
 
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<h3>Usage and Biology</h3>
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The set of BlcR mutants (</html>[[Part:BBa_K4361300]] through [[Part:BBa_K4361319]]<html>) were expressed in a PURE system in the presence of GreenLys (fluorescent Cy2-labeled lysine). Samples were then run on an SDS PAGE gel (<b>Figure 1.</b>) to determine whether or not the protein was produced. For this mutant (<u>lane 3</u>), a protein band corresponding to the BlcR monomer is visible. Concluding that the production in an E. coli cell-free system was successful for this mutant.
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<a href="https://static.igem.wiki/teams/4361/wiki/results/figure-7-pure/figure-7-pure-3.png"><img src="https://static.igem.wiki/teams/4361/wiki/results/figure-7-pure/figure-7-pure-3.png" style="width:600px;margin-left:125px"></a>
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<figcaption> <b>Figure 1.</b> SDS PAGE showing the translation products of 20 different plasmids coding for BlcR mutants. PURE reaction solution was supplemented with GreenLys and the synthesized proteins were imaged with Typhoon using a 488-nm laser. C: negative control with no plasmid. WT: positive control with expressed wildtype BlcR. 3: A40V mutant.</figcaption>
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</html>
  
 
<!-- Uncomment this to enable Functional Parameter display  
 
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Latest revision as of 18:15, 13 October 2022


BlcR A40V

A mutant of the BlcR protein, created through site-directed mutagenesis with primers R4 (Part:BBa_K4361204) and F4.1 A40V (Part:BBa_K4361205). For this mutant, the alanine in position 40 has been changed to valine by mutating the GCG codon to GTG.

This mutant also contains the following nucleotide mutations outside of the targeted site:

  • G 474 > T, silent mutation
  • T 529 > C, resulting in substitution F177L
  • G 606 > T, silent mutation
  • T 618 > A, silent mutation
  • G 648 > T, resulting in substitution E216D
  • T 681 > A, resulting in substitution E227D
  • G 742 > A, resulting in substitution E248A
  • A 745 > C, resulting in substitution K249Q

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 694
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 78
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 589

Usage and Biology

The set of BlcR mutants (Part:BBa_K4361300 through Part:BBa_K4361319) were expressed in a PURE system in the presence of GreenLys (fluorescent Cy2-labeled lysine). Samples were then run on an SDS PAGE gel (Figure 1.) to determine whether or not the protein was produced. For this mutant (lane 3), a protein band corresponding to the BlcR monomer is visible. Concluding that the production in an E. coli cell-free system was successful for this mutant.
Figure 1. SDS PAGE showing the translation products of 20 different plasmids coding for BlcR mutants. PURE reaction solution was supplemented with GreenLys and the synthesized proteins were imaged with Typhoon using a 488-nm laser. C: negative control with no plasmid. WT: positive control with expressed wildtype BlcR. 3: A40V mutant.