Difference between revisions of "Part:BBa K4035009"
 
(5 intermediate revisions by the same user not shown)
Line 4: Line 4:
  
  
−
This part is made of the Gal1 promoter ([https://parts.igem.org/Part:BBa_J63006 BBa_J63006]), the A-agglutinin-binding subunit Aga2 ([https://parts.igem.org/Part:BBa_K416000 BBa_K416000]) linked to the dimer protein CUP1-(GGGGS)3-CUP1 ([https://parts.igem.org/Part:BBa_K4035002 BBa_K4035002]) and the V5 tag ([https://parts.igem.org/Part:BBa_T2020 BBa_T2020]).
+
This part is the expression system of the CUP1 dimer ([https://parts.igem.org/Part:BBa_K4035002 BBa_K4035002]). It has been made by inserting the sequence into the pCTcon2-V5 plasmid (1) and is composed of the Gal1 promoter ([https://parts.igem.org/Part:BBa_J63006 BBa_J63006]), the A-agglutinin-binding subunit Aga2 ([https://parts.igem.org/Part:BBa_K416000 BBa_K416000]) linked to the dimer protein CUP1-(GGGGS)3-CUP1 ([https://parts.igem.org/Part:BBa_K4035002 BBa_K4035002]) and the V5 tag ([https://parts.igem.org/Part:BBa_T2020 BBa_T2020]).
  
  
 
==Usage and Biology==
 
==Usage and Biology==
  
−
Copper metallothionein CUP1 ([https://parts.igem.org/Part:BBa_M45090 BBa_M45090]) is a protein responsible for copper binding protein in the yeast Saccharomyces cerevisiae. In order to increase the copper retrieval efficiency, two copies of CUP1 were linked together and expressed on the external surface of S. cerevisiae by fusion with the A-agglutinin-binding subunit Aga2 ([https://parts.igem.org/Part:BBa_K416000 BBa_K416000]). Aga2 attaches to the yeast cell wall through disulfide bonds to Aga1p. The fusion of the dimer and Aga2 then leads to the presence of the CUP1 dimer on the outer membrane of the cell. The goal behind it was to improve the endogenous bio-accumulation property of wild type yeast by allowing it to bind more copper ions on its external surface.
+
Copper metallothionein CUP1 ([https://parts.igem.org/Part:BBa_M45090 BBa_M45090]) is a protein responsible for copper binding protein in the yeast Saccharomyces cerevisiae. In order to increase the copper retrieval efficiency, two copies of CUP1 were linked together ([https://parts.igem.org/Part:BBa_K4035002 BBa_K4035002]) and expressed on the external surface of S. cerevisiae by fusion with the A-agglutinin-binding subunit Aga2 ([https://parts.igem.org/Part:BBa_K416000 BBa_K416000]). Aga2 attaches to the yeast cell wall through disulfide bonds to Aga1p. The fusion of the dimer and Aga2 then leads to the presence of the CUP1 dimer on the outer membrane of the cell. The goal behind it was to improve the endogenous bio-accumulation property of wild type yeast by allowing it to bind more copper ions on its external surface.
  
 
This fusion protein also contains a V5 tag ([https://parts.igem.org/Part:BBa_T2020 BBa_T2020]) in order to check its expression by Western Blot and Immunocytochemistry. The expression is under the control of the Gal1 promoter ([https://parts.igem.org/Part:BBa_J63006 BBa_J63006]), so that the protein is expressed only in the presence of galactose.
 
This fusion protein also contains a V5 tag ([https://parts.igem.org/Part:BBa_T2020 BBa_T2020]) in order to check its expression by Western Blot and Immunocytochemistry. The expression is under the control of the Gal1 promoter ([https://parts.igem.org/Part:BBa_J63006 BBa_J63006]), so that the protein is expressed only in the presence of galactose.
Line 17: Line 17:
 
==Sequence and Features==
 
==Sequence and Features==
 
<partinfo>BBa_K4035009 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K4035009 SequenceAndFeatures</partinfo>
 +
  
  
Line 22: Line 23:
 
==Characterization==
 
==Characterization==
  
−
The characterization of this part can be found on the [https://parts.igem.org/Part:BBa_K4035002 Part:BBa K4035002] page as this one is describing its expression system.
+
The characterization of this part can be found on the [https://parts.igem.org/Part:BBa_K4035002 Part:BBa K4035002] page describing the dimer sequence.
  
  

Latest revision as of 20:42, 21 October 2021


Expression of the CUP1-(GGGGS)3-CUP1 dimer on the extracellular membrane of S. cerevisiae


This part is the expression system of the CUP1 dimer (BBa_K4035002). It has been made by inserting the sequence into the pCTcon2-V5 plasmid (1) and is composed of the Gal1 promoter (BBa_J63006), the A-agglutinin-binding subunit Aga2 (BBa_K416000) linked to the dimer protein CUP1-(GGGGS)3-CUP1 (BBa_K4035002) and the V5 tag (BBa_T2020).


Usage and Biology

Copper metallothionein CUP1 (BBa_M45090) is a protein responsible for copper binding protein in the yeast Saccharomyces cerevisiae. In order to increase the copper retrieval efficiency, two copies of CUP1 were linked together (BBa_K4035002) and expressed on the external surface of S. cerevisiae by fusion with the A-agglutinin-binding subunit Aga2 (BBa_K416000). Aga2 attaches to the yeast cell wall through disulfide bonds to Aga1p. The fusion of the dimer and Aga2 then leads to the presence of the CUP1 dimer on the outer membrane of the cell. The goal behind it was to improve the endogenous bio-accumulation property of wild type yeast by allowing it to bind more copper ions on its external surface.

This fusion protein also contains a V5 tag (BBa_T2020) in order to check its expression by Western Blot and Immunocytochemistry. The expression is under the control of the Gal1 promoter (BBa_J63006), so that the protein is expressed only in the presence of galactose.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1000
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 150
  • 1000
    COMPATIBLE WITH RFC[1000]



Characterization

The characterization of this part can be found on the Part:BBa K4035002 page describing the dimer sequence.