Difference between revisions of "Part:BBa K1355002:Design"

Revision as of 00:39, 9 October 2014

Mercury ions detector device

Design Notes

For this genetic construction, we followed these summarized steps in the following image:

1) Transformation of DH5-alpha with the Green Fluorescent Protein (GFP) translational unit BBa_E0840 and with the Essential Biobrick (Regulation and transport of mercury) BBa_K1355001 that contains a bidiretional promotor regulated by the MerR protein.

2) Extraction and quantification of the BBa_E0840 and BBa_K1355001 plasmid DNA;

2) Verifying the electrophoretic profile of the extracted plasmid DNA;

Figure 1: A) Electrophoretic profile of BBa_E0840 plasmid DNA in pSB1C3; B) Eletrophoretic of BBa_K1355001 plasmid DNA in pBSK.

3) Restriction enzyme digestion of the BBa_K1355001 with SpeI and EcoRI and of BBa_E0840 with EcoRI and XbaI aiming to isolate the biobrick fragment and linearize the vector, respectively;

4) Checking the electrophoretic profile of digested samples;

Figura 2: A) Electrophoretic profile of BBa_K1355001 digested with SpeI and EcoRI; B) Eletrophoretic profile of the BBa_E0840 digested with EcoRI and XbaI.

5) Purification from agarose gel of the fragment (Biobrick BBa_K1355001) and the linearized vector (BBa_E0840);

4) Checking the electrophoretic profile of purified samples;

Figure 3: A) Eletrophoretic profile of BBa_K1355001 (fragment) purified; B) Eletrophoretic profile of BBa_E0840 (linearized vector) purified.

6) Ligation of the linearized vector with fragment using T4 DNA ligase;

7) Transformation of the ligation in DH5-alpha;

FOTO

Figure 4: Mercury Bacter Hg biodetector (DH5-alpha transformed with BBa_K1355002)

8) Extraction of plasmid DNA with our biodetector constrution from DH5-alpha transformed;

9) Check the electrophoretic profile to see results of samples linked;

Figure 5: Electrophoretic profile of BBa_K1355002 plasmid DNA in pSB1C3.

10) Restriction enzyme digestion of BBa_K1355001 + BBa_E0840 (BBa_K1355002) with EcoRI + PstI, and only with EcoRI aiming to analyze the fragment size to be isolated (digestion with EcoRI + PstI) and the size of the linearized vector (digestion only with EcoRI);

11) Checking the electrophoretic profile of the digested sample to obtain results showing that the isolated fragment (sample digested with EcoRI + PstI) is the junction of BBa_K1355001 + BBa_E0840 in pSB1C3 and that the linearized vector (sample digested only with EcoRI) is our biobrick in pSB1C3;

Figure 6: Eletrophoretic profile of the BBa_K1355003 do not digested; digested only with EcoRI; digested only with PstI; and digested with EcoRI + PstI, respectively.

Source

BBa_K1355001, BBa_E0840

References