Team:Newcastle/26 August 2010

From 2010.igem.org

Revision as of 15:01, 7 September 2010 by Alankoh (Talk | contribs)

iGEM Homepage Newcastle University BacillaFilla Homepage Image Map

Contents

yneA

PCR (Repeat)

Aim

To repeat the PCR that we did yesterday using the correct rocF primers.

Materials and Protocol

Please refer to PCR.


PCR Purification

Aim

To remove unwanted primers, taq polymerase, buffer and salts to obtain pure DNA.

Materials and Protocol

Please refer to PCR purification.


Restriction Digest

Aim

To digest the PCR products of pSB1C3 and yneA from PCR purification with enzymes EcoR1 and Nhe1.

Materials and Protocol

Please refer to restriction digest.

Results, Discussion and Conclusion

We run the digested products with gel electrophoresis to determine whether the digest worked.

Gel extraction

Aim

To purify the DNA of yneA and pSB1C3 by extracting the bands from the gel after running gel electrophoresis. Concentration of DNA is then checked with NanoDrop.

Materials and Protocol

Please refer to:

Results

The gel did not show any band when we looked at it from GelDoc.

Conclusion

The restriction digest did not work, so we will repeat the protocol again tomorrow.

First transformation of 'Bacillius subtilis 168' with Prrnb-GFP containing YneA

Aim

The aim of the experiment is to perform insert the plasmid Prrnb-GFP containing YneA which have been ligated eariler into the chromosome of 'Bacillus subtilis 168'. 'B. subtilis' containing the intergated vector will be resistance to both the antibiotic chloramphenicol and streptomycin, therefore those that have successful intergated will be selected with agar plates that contain these antibiotic. The second step will be to identify those colones that have the plasmid intergated at the corerct position in the chromosome, which is the amylase locus. Thus those that have intergardted at the wrong position will not be able to break down starch, which can be tested with the iodine test.

Materials and Protocol

Please refer to: Transformation of Bacillus subtilis Note: Overnigth culture of 'B. subtilis 168' in MM competence medium was done the day before and the iodine test was performed the day after.

Results

Unfortunately our colonies had halos. Although the insert has integrated, the colonies have antibiotic restistance, the insert has not integrated at the amyE locus.


Starchplate.jpg
Starchplate2.jpg

However when we checked the colonies under a microscope the cells were filamentous due to integration elsewhere on the Bacillus subtilis 168 chromosome perhaps at the native yneA locus.

Filamentous cells
Filamentous cells showing GFP signal
Normal Bacillus subtilis 168



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