Regulatory

Part:BBa_K3189001:Experience

Designed by: Jehoshua Sharma, Nathanael Wilms, Connor Gianetto-Hill   Group: iGEM19_Guelph   (2019-10-16)


This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_K3189001


GFP Expression using BBa_K3189001

The flasks in Figure 1 shows 50 mL E.coli cells transformed with gfp under the control of BBa_K3189001. On the plasmid containing BBa_K3189001 is the repressor, BBa_K3189004, needed for proper function of the promoter. Tetracycline was used to induce the system, resulting in GFP production and fluorescence is seen using a UV wand.

T--Guelph--tetO_characterization.JPG
Figure 1: E. coli cells expressing GFP under the control of BBa_K3189001 induced with tetracycline.

An initial expression test of GFP under the control of BBa_K3189001 was preformed using 1 ng/mL and 50 ng/mL tetracycline. It can be seen in Figure 2 that more fluorescence was seen with the higher concentration of tetracycline. Based on these results it seems that BBa_K3189001 responds to tetracycline in a dose dependent manner.

T--Guelph--GPRexpression.PNG
Figure 2: E. coli strains DH5a and BL21(DE3) expressing GFP under the control of BBa_K3189001 using 1 ng/mL and 50 ng/mL tetracycline.

To determine what levels of tetracycline are needed to induce expression of GFP downstream of BBa_K3189001, a minimum inhibitory concentration (MIC) like test was preformed using decreasing level of tetracycline. The tetracycline levels used started at 10,000 ng/mL in the first column of the plate in Figure 3 and reduced by half in each subsequent well until reaching 0.01 ng/mL. This plate was imaged using an UV light table. Visually it can be seen that the brightest wells are at 312.5 ng/mL for E. coli BL21(DE3) with little to no fluorescence was observed E. coli DH5a.

800px-T--Guelph--96-well_plate.jpeg
Figure 3: GFP under the control of BBa_K3189001 expression at decreasing levels of tetracycline.



BBa_K3189001 in BBa_K3189015

The construct BBa_K3189015 containing the chromoprotein amilCP (BBa_K1343022) under the control of BBa_K3189001. When the system is induced with 100 ng/mL of tetracycline, a dark blue colour is produced (Figure 4 and Figure 5). This shows BBa_K3189001 is able to function with different reporter proteins other than just gfp.

216px-T--Guelph--pTA-tetnotet.jpg
Figure 4: BBa_K2669002 under the control of BBa_K3189001. amilCP expression being induced using 100 ng/mL tetracycline (left) and uninduced (right).

207px-T--Guelph--pTAtetnotetspun.jpg
Figure 5: Pellets of cells of BBa_K2669002 under the control of BBa_K3189001 induced and uninduced with tetracycline. Pellet of cells induced with 100 ng/mL tetracycline (left) and pellet of cells uninduced (right).


User Reviews

UNIQ564633ea3de7b516-partinfo-00000000-QINU UNIQ564633ea3de7b516-partinfo-00000001-QINU