Team:LCG-UNAM-Mexico:Journals:Uriel
From 2009.igem.org
(Difference between revisions)
(→August 4, 2009) |
(→References) |
||
(29 intermediate revisions not shown) | |||
Line 134: | Line 134: | ||
== August 4, 2009 == | == August 4, 2009 == | ||
- | [Image:5-ago-dr para ligar.jpg] | + | [[Image:5-ago-dr para ligar.jpg|200px]] |
We redo the colony PCR for [http://partsregistry.org/Part:BBa_K242001 ogr] and [http://partsregistry.org/Part:BBa_K242002 cox] only using the [https://2009.igem.org/Team:LCG-UNAM-Mexico/Resources/Strains C-117] strain. The PCR | We redo the colony PCR for [http://partsregistry.org/Part:BBa_K242001 ogr] and [http://partsregistry.org/Part:BBa_K242002 cox] only using the [https://2009.igem.org/Team:LCG-UNAM-Mexico/Resources/Strains C-117] strain. The PCR | ||
Line 375: | Line 375: | ||
[https://2009.igem.org/Team:LCG-UNAM-Mexico/Resources/Strains DH5alpha] strains that contain the listed plasmids below were grown in selective media and plasmid | [https://2009.igem.org/Team:LCG-UNAM-Mexico/Resources/Strains DH5alpha] strains that contain the listed plasmids below were grown in selective media and plasmid | ||
purification was performed and afterwards it was digested. | purification was performed and afterwards it was digested. | ||
+ | |||
+ | |||
Plasmids: | Plasmids: | ||
- | 1) | + | 1) ogr XbaI/PstI |
- | 2) | + | 2) ogr+pSB1CB XbaI/PstI |
- | 3) | + | 3) ogr+pSB1CB EcoRI/PstI |
- | 4) | + | 4) ogr+pSB1CB EcoRI/PstI |
- | 5) | + | 5) ogr+pSB1CB EcoRI/PstI |
- | 6) | + | 6) BBa_J04450 EcoRI/PstI |
- | 7) | + | 7) ogr+BBa_PB1005 EcoRI/PstI |
- | 8) | + | 8) BBa_J04450 EcoRI/PstI |
+ | 9) cox | ||
Restriction Reactions: | Restriction Reactions: | ||
Line 403: | Line 406: | ||
With this gel was confirmed that [http://partsregistry.org/Part:BBa_K242001 ogr] is cloned in [http://partsregistry.org/Part:pSB1T3 pSB1T3] and now we can make a glycerol for this strain. | With this gel was confirmed that [http://partsregistry.org/Part:BBa_K242001 ogr] is cloned in [http://partsregistry.org/Part:pSB1T3 pSB1T3] and now we can make a glycerol for this strain. | ||
- | 24 Ago 2009 | + | [[Image:21-08-09--ogrpcr-4xogr+18-17-cox-17-ogr+ter.jpg|200px ]] |
+ | |||
+ | First nine lanes interest. | ||
+ | |||
+ | == 24 Ago 2009 == | ||
- | The | + | The pSB1C3 was dephosphorylated with antarctic phosphate |
Dephospohrialtion Reaction: | Dephospohrialtion Reaction: | ||
Line 420: | Line 427: | ||
2) 5 min --> 65ºC | 2) 5 min --> 65ºC | ||
- | After plasmid dephosphorialtion we are going to perform a ligation reaction between | + | After plasmid dephosphorialtion we are going to perform a ligation reaction between cox and ogr+BBa_0015 |
== August 25, 2009 == | == August 25, 2009 == | ||
Line 449: | Line 456: | ||
We platted [https://2009.igem.org/Team:LCG-UNAM-Mexico/Resources/Strains DH5alpha] transformed cells over selective medium and incubate the plates overnight at 37ºC. | We platted [https://2009.igem.org/Team:LCG-UNAM-Mexico/Resources/Strains DH5alpha] transformed cells over selective medium and incubate the plates overnight at 37ºC. | ||
+ | |||
+ | == August 27, 2009 == | ||
+ | |||
+ | Plasmid extraction | ||
+ | |||
+ | [[Image:3x024-pcrcontrol-x007.jpg|250px]] | ||
== August 29, 2009 == | == August 29, 2009 == | ||
Line 471: | Line 484: | ||
We run a 1% Agarose gel at 85 V. 1hr | We run a 1% Agarose gel at 85 V. 1hr | ||
+ | |||
+ | [[Image:Ogr+ter-cox-17dfos.jpg|250px]] | ||
Unfortunately [http://partsregistry.org/Part:BBa_K242002 cox]+[http://partsregistry.org/Part:BBa_K242001 ogr]+BBa_B0015 cloning by fusing [http://partsregistry.org/Part:BBa_K242002 cox] and [http://partsregistry.org/Part:BBa_K242001 ogr]+BBa_B0015 in another plasmid | Unfortunately [http://partsregistry.org/Part:BBa_K242002 cox]+[http://partsregistry.org/Part:BBa_K242001 ogr]+BBa_B0015 cloning by fusing [http://partsregistry.org/Part:BBa_K242002 cox] and [http://partsregistry.org/Part:BBa_K242001 ogr]+BBa_B0015 in another plasmid | ||
didn't work out. We will try to repeat the procedure to see if we are luckier. | didn't work out. We will try to repeat the procedure to see if we are luckier. | ||
- | |||
== September 7, 2009 == | == September 7, 2009 == | ||
Line 696: | Line 710: | ||
== October 5, 2009 == | == October 5, 2009 == | ||
- | To test for the activity of the [http://partsregistry.org/Part:BBa_K242100 multipromoter] that we | + | To test for the activity of the [http://partsregistry.org/Part:BBa_K242100 multipromoter] that we designed and synthesized, we are going to |
- | transform E. coli [https://2009.igem.org/Team:LCG-UNAM-Mexico/Resources/Strains#Expression_Strains BL21(DE3)plysS] | + | transform E. coli [https://2009.igem.org/Team:LCG-UNAM-Mexico/Resources/Strains#Expression_Strains BL21(DE3)plysS] from novagen. This strain uses a T7 phage polymerase that is controlled thorough Lac promoter. The multipromoter is composed of T7 & T3 promoters, we expect that our construction will respond to IPTG. |
- | This strain uses a T7 phage polymerase that is controlled | + | |
- | + | The IPTG preparation protocol we used is discribed [http://openwetware.org/wiki/IPTG HERE!!!] | |
- | + | ||
- | + | Transformed cells were platted on LB medium with Kn and IPTG .5 mM and expect that the colonies will fluoresce | |
+ | and could be seeing with a transluminator. | ||
- | + | == Octuber 6, 2009 == | |
- | + | We took a look to the LB Agar plates with a transluminator at a wavelength of 395nm but because we didn't have a | |
- | + | filter for GFP emitting wavelength we couldn't discriminate for our wavelength of interest. | |
- | + | We are going to try other approach this time with a microscope more suitable to see GFP. | |
- | + | ||
- | + | == October 7, 2009 == | |
+ | |||
+ | REGISTRY SITE FOR [http://partsregistry.org/wiki/index.php?title=Part:BBa_K242101 MULTIPROMOTER] BBa_K242101 | ||
+ | |||
+ | m stands for multipromoter !! | ||
+ | |||
+ | Cultures were prepared as follows: | ||
+ | |||
+ | BL21/m+ BL21/m+ BL21/m- | ||
+ | 100 mL LB + + + | ||
+ | 100 µL Kan 30 µg/µL + + - | ||
+ | 100 µL Cam 20 µg/µL + + + | ||
+ | 10 µL IPTG 1M + - + | ||
+ | |||
+ | |||
+ | For the induction of protein production we started our culture at .1 abs 620nm in 100mL LB and waited until it reached 0.35 abs 620 nm then we added IPTG to a final concentration of 0.1mM and then we leave the culture media for four | ||
+ | hours. | ||
+ | |||
+ | 5mL of each culture were centrifuged at max speed and the supernatant was discarded. We prepared our samples | ||
+ | to see them. Using a microscope with suitable filters and light to see GFP we compared the cultures between them | ||
+ | |||
+ | Results: | ||
+ | Bl21/m+ Bl21/m+ Bl21/m- | ||
+ | IPTG + - + | ||
+ | ++++ ++ - Fluorescence | ||
[[Image:Gfp multi.JPG |280px]] | [[Image:Gfp multi.JPG |280px]] | ||
- | Great NEWS!!! our promoter worked for T7 polymerase | + | In frame is BL21/multipromoter with IPTG inducer at 100X. Unfortunately the microscope and camera were not suitable to check in full detail BL21/m- IPTG+, which gave no fluorescence, and Bl21/multipromoter IPTG-, which presented a diminished fluorescence. |
+ | |||
+ | This results support the functioning of multipromoter for T7 polymerase. | ||
+ | |||
+ | Great NEWS!!! our promoter worked for T7 RNA polymerase | ||
+ | |||
+ | For future experiments to get a better characterization look result site. | ||
== October 20, 2009 == | == October 20, 2009 == | ||
Line 733: | Line 775: | ||
== October 21, 2009 == | == October 21, 2009 == | ||
+ | Preparation of parts for sending them to the registry!!! | ||
+ | =References= | ||
+ | To see all the literature that we used to develop the construction of control system pleas visit | ||
+ | references site and look for ogr, cox, P2 and P4 papers [https://2009.igem.org/Team:LCG-UNAM-Mexico/Description#References References]. | ||
<!--Do not remove the first and last lines in this page!-->{{Template:LCG_bottom_Netscape}} | <!--Do not remove the first and last lines in this page!-->{{Template:LCG_bottom_Netscape}} |
Latest revision as of 03:48, 22 October 2009