Team:Newcastle/3 September 2010

From 2010.igem.org

(Difference between revisions)
(Results)
(Levan glue)
 
(6 intermediate revisions not shown)
Line 1: Line 1:
{{Team:Newcastle/mainbanner}}
{{Team:Newcastle/mainbanner}}
-
=''yneA''=
+
=Levan glue=
-
==Aims==
+
We started working on levan. For this we used agar plates containing 10% sucrose and ''Bacillus subtilis'' 168 was grown onto that medium. The sucrose cultures and controls were compared. The cultures grown on sucrose should be considerably thicker.
-
The aim of the experiment is to test for the correct integration of ''yne''A in pGFPrrnb plasmid.
+
The overnight cultures of the different strains were also grown on solid agar plates with and without sucrose.
 +
For more information levan, please refer to: [[Team:Newcastle/glue|levan]].
-
==Materials and protocols==
+
[[Image:DSC01022.JPG|500px|''B. subtilis producing levan]]
-
#Please refer to: [[Team:Newcastle/Qiagen_Minipreps#Plasmid_extraction| Plasmid extraction]].
+
'''Image 1''': Image showing ''B. subtilis'' producing levan on agar plate containing 10% sucrose.
-
#Please refer to:[[Team:Newcastle/Restriction_digests|Restriction digest]]. We used Nhe1 and Spe1 to remove the ''yneA'' from pGFP-rrnB.
+
-
#Please refer to:[[Team:Newcastle/Gel_electrophoresis| Gel electrophoresis]] for running all the digested plasmid fragments.
+
-
==Results==
 
-
 
-
[[Image:03.09.10.png#file|400px]]
 
-
 
-
'''Figure 1''': Restriction digest result of pGFPrrnB and ''yneA'' with Nhe1 and Spe1.
 
-
 
-
* '''Lane 1''': 1kb DNA ladder
 
-
* '''Lane 2''': Tube 1
 
-
* '''Lane 3''': Tube 2
 
-
* '''Lane 4''': Tube 3
 
-
* '''Lane 5''': Tube 4
 
-
* '''Lane 6''': Tube 5
 
-
* '''Lane 7''': Tube 6
 
-
* '''Lane 8''': Tube 7
 
-
* '''Lane 9''': Tube 8
 
-
* '''Lane 10''': Tube 9
 
-
* '''Lane 11''': Tube 10
 
-
* '''Lane 12''': Tube 11
 
-
* '''Lane 13''': Tube 12
 
-
* '''Lane 14''': 1kb DNA ladder
 
-
 
-
==Conclusion==
 
-
 
-
The results show that the digest works, there is a band at approximately 541bp corresponding to ''yneA'' and a band at approximately 8.4kbp corresponding to pGFPrrnb in lanes 2,3,4,6,7,8,9, 11 and 12.
 
{{Team:Newcastle/footer}}
{{Team:Newcastle/footer}}

Latest revision as of 02:08, 28 October 2010

iGEM Homepage Newcastle University BacillaFilla Homepage Image Map

Levan glue

We started working on levan. For this we used agar plates containing 10% sucrose and Bacillus subtilis 168 was grown onto that medium. The sucrose cultures and controls were compared. The cultures grown on sucrose should be considerably thicker.

The overnight cultures of the different strains were also grown on solid agar plates with and without sucrose. For more information levan, please refer to: levan.

B. subtilis producing levan

Image 1: Image showing B. subtilis producing levan on agar plate containing 10% sucrose.


Newcastle University logo.png    Newcastle cbcb logo.pngNewcastle Biomedicine logo.gif    Team Newcastle CEG logo.gif
Newcastle iww logo.jpg  UNIPV Pavia Logo.gif  Newcastle BBSRC.gif    Newcastle Genevision logo.png Newcastle WelcomeTrust.jpg
FaceBook Icon