Week 6
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''-idem after 2 hours.'' | ''-idem after 2 hours.'' | ||
- | + | We check bacteria from the stock and we see that some of them are fluorescent, even if we don’t expect this result. | |
- | *We strake on plate from falcon with glucose, we discard the supernatant, we clean in LB for 2 times, we | + | *We strake on plate from falcon with glucose, we discard the supernatant, we clean in LB for 2 times, we resuspend in 5 ml of LB. Bacteria become fluorescent. When we add 2 mM of glucose the bacteria are no fluorescent. |
- | + | ||
- | We are going to insert in our construct | + | So, it is possible to control Plac activation with glucose. As it's known in literature, endogenous LacI is not enough to repress Plac promoter from a high copy number plasmid and a small amount of glucose arises the cinetic rateo of Plac trascription. |
+ | We are going to insert LacI in our construct to solve this problem. | ||
This test enables us to verify GFP emivita which is about 40 minutes (link literature). | This test enables us to verify GFP emivita which is about 40 minutes (link literature). | ||
*[http://partsregistry.org/Part:BBa_J04431 J04431] digestion with Eco/Xba; | *[http://partsregistry.org/Part:BBa_J04431 J04431] digestion with Eco/Xba; |
Revision as of 13:52, 3 September 2007
- 08/06/07
- I763005 digestion with Spe1/Pst1;
- Ligation for J04500+J22101 (I763012);
- We inoculate in 5 ml for P0412, R0010.
- 08/07/07
- Miniprep for P0412 and R0010.
- We inoculate a colony of J04431 in 5 ml to perform the fluorescence test with glucose (see the following protocol).
J04431 bacteria from glycerol stock:
-growth of 1 ml 10 aliquot at 37°C for 1h;
-collection of 5 ml in 2 falcon;
-fluorescence control (1 green, 1 not);
-add glucose 2 mM in each falcon;
-incubation at 37°C for 1 h;
-in each falcon there aren't fluorescence bacteria;
-idem after 2 hours.
We check bacteria from the stock and we see that some of them are fluorescent, even if we don’t expect this result.
- We strake on plate from falcon with glucose, we discard the supernatant, we clean in LB for 2 times, we resuspend in 5 ml of LB. Bacteria become fluorescent. When we add 2 mM of glucose the bacteria are no fluorescent.
So, it is possible to control Plac activation with glucose. As it's known in literature, endogenous LacI is not enough to repress Plac promoter from a high copy number plasmid and a small amount of glucose arises the cinetic rateo of Plac trascription. We are going to insert LacI in our construct to solve this problem. This test enables us to verify GFP emivita which is about 40 minutes (link literature).
- J04431 digestion with Eco/Xba;
- B0015 digestion with Eco/Xba;
- P0412 digestion with Xba/Pst1;
- J04431, B0015, P0412 band extraction;
- Transformation of J04500+J22101 (I763012) ligation.
- 08/08/07
- Model analysis.
- 08/09/07
- 08/10/07
- Miniprep of I763012 and of I763016;
- I763012 digestion with Spe1/Pst1;
- I763012 control digestion with Xba/Pst1;
- I763012 extraction from gel.