Revision as of 09:52, 4 August 2012

Notebook: Week 8

Aims of the Week

The Lab team are aiming to begin assembly of Ribosome Binding Site and Constitutive Promoter, which could then be used for a number of our modules. James and Leonard have also been working towards characterising salt tolerance, and aim to begin doing this by the end of the week. The protocol for this experiment has been decided, and so it is likely we will have some characterisation data by the end of the week. Rhiannon's aim was to finish setting up the wiki LabBook, and publish it on the wiki. The Rathenau Debate Deadline is approaching, and Erin plans to make the final touches before it is sent off. Carina also wants to confirm her plans for the architectural project and begin a diary documenting her designs.

Monday 30th July

Wet Lab. After the concern that the small size of the BBa_J23119 and BBa_B0034 insert means we cannot truly detect the presence of the correct insert (Ext 7.3), Rhiannon and Aurelija decided to investigate other ways of detecting it. This included setting up a 25bp ladder on 3.5% gel, but neither the 12bp insert (BBa_B0034) or the 35bp insert (BBa_J23119) could be detected. This may be due to the low concentration of these plasmids - and so we are considering using PCR to amplify them.

Meeting - wiki. Rhiannon met with many of the team members to discuss the design for the Lab Book page. Our aim was to make the work description sufficiently detailed that it could be easily reproduced by others in the future. At the same time, we risked making it too long to read. For this reason, we have a summary infographic for each class of experiments, which clearly illustrate the method and results. However, we have also contained all of the necessary information in a drop-down from this image. While the design will continue to evolve, we are currently content with it at present.

Tuesday 31st July

Wet Lab. Todays activities included PCR reactions of plasmid backbones, to amplify them before use, and analysis of their concentration by nanodrop. This proved somewhat disappointing. There was also miniprep of our Tetracycline Repressor (BBa_C0040) and the Gas Vesicle Cluster (BBa_I750016), but both proved to have very low [plasmid concentration. We also grew up some of our W3100 cells transformed with the Salt Tolerance BioBrick (BBa_K398108), as well as some untransformed W3100s, for characterisation of salt tolerance tomorrow.

Rathenau. Erin finished her write up of the Rathenau debate, and after proof reading from other members of the team sent it to an advisor for assessment.

Wednesday 1st August

Wet Lab:Today James began characterisation of the salt tolerance BioBrick. We used a simple protocol, involving 3 different salt concentrations for a transformed and untransformed line of W3100s. We also commenced 3A assembly and transformation of our Constitutive Promoter (J23119), the stress promoter (PcstA), the Ribosome Binding Site (BBa_B0034) and the plasmid backbone PSB1K3. An analytical digest of our plasmid backbones proved disappointing, as so we began a repeat of the PCR. We also re-picked colonies of the BBa_C0040 and BBa_R0040 BioBricks, which have proven very difficult to transform and culture.

Modelling - meeting with Chris Barnes: Chris Barnes is a member of UCL staff who created the ACBsysBio software during his days in Imperial. We had already talked to Chris Barnes about how his software was going to be useful for our project. This meeting was to check how our initial model, written in MATLAB SimBiology, would be transported across into his software. Outcome: It appears the the model will work.

Thursday 2nd August

Wetlab: James completed the protocol for the salt characterisation, which appears to have been successful. This will be repeated early next week. There was also a gel for the repeat of the PCR of plasmid backbones, which again proved unsuccessful - for reasons that are not clear to us.

Also given the problems we have had with transformation - we have set up another series on transformations, which will attempt to eliminate some of the causes of problems already experienced. We are also allowing only two members of the team to carry out the protocol from start to finish, to limit the number of possible problems. BioBricks that are being transformed are the Constitutive Promoter (BBa_J23119) and Ribosome Binding Site (BBa_B0034) due to their low concentration. Also included is a a spare Constitutive Promoter (BBa_J23100) and a spare Ribosome Binding Site (BBa_B0030)

@@ Line 19: / Line 19: @@
 == Tuesday 31st July ==
-<div class="notebook-wetlab"> '''Wet Lab.''' Todays activities included PCR reactions of plasmid backbones, and analysis of their concentration by nanodrop. This proved somewhat disappointing. There was also miniprep of our Tetracycline Repressor (BBa_C0040) and the Gas Vesicle Cluster (BBa_I750016), but both proved to have very low [plasmid concentration. We also grew up some of our W3100 cells transformed with the Salt Tolerance BioBrick (BBa_K398108), as well as some untransformed W3100s, for characterisation of salt tolerance tomorrow.</div>
+<div class="notebook-wetlab"> '''Wet Lab.''' Todays activities included PCR reactions of plasmid backbones, to amplify them before use, and analysis of their concentration by nanodrop. This proved somewhat disappointing. There was also miniprep of our Tetracycline Repressor (BBa_C0040) and the Gas Vesicle Cluster (BBa_I750016), but both proved to have very low [plasmid concentration. We also grew up some of our W3100 cells transformed with the Salt Tolerance BioBrick (BBa_K398108), as well as some untransformed W3100s, for characterisation of salt tolerance tomorrow.</div>
 <div class="notebook-rathenau"> '''Rathenau.''' Erin finished her write up of the Rathenau debate, and after proof reading from other members of the team sent it to an advisor for assessment. </div>

Team:University College London/Notebook/Week8

From 2012.igem.org