Team:Heidelberg LSL/Notebook methods

From 2012hs.igem.org

Revision as of 19:29, 11 June 2012 by Bunnech (Talk | contribs)

iGEM-2012HS - LSL-Heidelberg iGEM-2012HS - LSL-Heidelberg

Methods

Transformation

Transformation is a process in which linear or circular DNA, in other words your designed plasmid, is brought into competent bacteria without the help of bacteriophages. You do this mostly with one of these two intentions: firstly, you want to amplify of your chosen Biobrick-DNA and let transformed bacteria grow it for you is the cheapest and fastest way. Afterwards you have to extract your chosen Biobrick out of your bacteria. Secondly, when you completed your construct in form of a plasmid, you might need to bring it into your final bacteria cells to test if it works.
For amplifying DNA from the registry, we transformed chemocompetent Top10 cells by applying the following protocol:
DNA from Registry Plate: 10 ul water is added to the corresponding well containing the desired BioBrick DNA and DNA is solved by incubation for 15 min at room temperature. 5 ul of DNA solution are added to 50 ul of chemocompetent Top10 cells and incubated on ice for 20 min. Afterwards, a heat shock is performed by incubation the bacteria on 42°C/50 s. After another 2 min on ice, the bacteria are plated onto LB-Amp agar plates.

Inoculation of LB agar plates

LB agar is made of LB medium substituted with 100 ug/ml ampicillin and 1.5 % Agar, which makes the LB media solidify.
When plating out transformed bacteria, you should start by carefully labelling the plate with the construct name, date, bacterial strain, antibiotic resistance and your initials and preheat the plate to 37° C. Using a bunsen burner, you then form an inoculation loop out of a small glass pipette. After adding 20-100 ul of bacterial suspension to the plate, you evenly distribute it on the agar plate surface with your glass tool. Now, you can incubate the inoculated LB agar plates at 37 degrees celsius overnight.

Inoculation of liquid LB medium

...

Qiagen Miniprep

With a Miniprep you extract DNA out of liquid bacterial suspensions such as overnight cultures. There are various companies that offer kits for this process. We followed the instructions of the Qiagen Miniprep kit or the Promega Miniprep kit according to the manufacturer's protocols.
DNA was eluted from the column using either 50 ul of water or TE buffer.

Restriction digest

A restriction digest is the process in which restriction enzymes, small selective DNA-scissors, cut DNA in pieces. These enzymes bind selectively at specific sequences and cut double-stranded DNA either blank or sticky (i.e. they produce up to 4 bp non-paired overhangs). You have to think carefully about the choice of the right restriction enzymes when making up your cloning strategy. For iGEM standard cloning in BBa-format as it was applied here, the following protocol can be applied for all Enzymes used (EcoRI, SpeI, XbaI, PstI).
We used the NEB restriction enzymes and buffers for setting up the digestions. Those were done as follows:
*1 µg of DNA
*3 µl of NEB buffer 2
*3 µl of BSA
*1 µl of each restriction enzyme used
*Water was added to reach a final volume of 30 ul

After setting up the digestions, the reaction mixtures were mixed briefly, spinned down in a centrifuge (quick run up to 5.000 rpm) and then incubated on a thermomixer heating device for 1 h at 37 °C and stored at -20 °C afterwards. After Digestion, DNA was purified via a qiagen nucleotide removal or gel extraction kit.

Contents

SAP digest

...

Gel electrophoresis

<p>...

Gel extraction

<p>...

Qiagen nucleotide removal kit

<p>...

Ligation digest

<p>...

Oligo annealing

<p>...

Colony PCR

<p>...

Sequencing

<p>...

X-Gal assay

<p>...

ONPG assay

<p>...

Use of the photometer

<p>...

Use of the plate reader

<p>...

<p> 

</div> </div>