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| | !align="center"|[[Team:University_of_Sheffield /Project|Our project]] | | !align="center"|[[Team:University_of_Sheffield /Project|Our project]] |
| | !align="center"|[[Team:University_of_Sheffield /Modelling|Modelling]] | | !align="center"|[[Team:University_of_Sheffield /Modelling|Modelling]] |
| - | !align="center"|[[Team:University_of_Sheffield /Parts|Parts]] | + | !align="center"|[[Team:University_of_Sheffield /Wet Lab|Wet Lab]] |
| - | !align="center"|[[Team:University_of_Sheffield /Lab Books| Our Team]] | + | !align="center"|[[Team:University_of_Sheffield /Lab Books| Our team]] |
| - | !align="center"|[[Team:University_of_Sheffield /Calendar| Calendar]] | + | !align="center"|[[Team:University_of_Sheffield /Timetable| Timetable]] |
| | + | !align="center"|[[Team:University_of_Sheffield /Misc| Miscellaneous]] |
| | |} | | |} |
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| | <!-- and finish cutting here! --> | | <!-- and finish cutting here! --> |
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| - | __TOC__
| + | =Our Team= |
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| - | ==Protocols==
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| - | ===Tecan Fluorescence Measurement===
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| - | Protocol used for characterization :
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| - | 1. Grow 5ml of overnight cultures of DH5-alpha cells containing the plasmid with GFP-LVA.
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| - | 2. Resuspend the overnight cultures in 50 ml of LB medium until the OD600 reaches about 0.6.
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| - | 3. Quickly add 0.2 mM of IPTG to the medium and plate that into 96 well plate.
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| - | 4. To 96 well plate add 180 ul of LB + IPTG as a control, 180 ul of DH5-alpha cells not induced with IPTG, finally add 180 ul of DH5-alpha induced with IPTG. Carry out the aforementioned in duplicates.
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| - | 5. Use the high flow cytometry machine Tecan to measure the fluorescence every 15 minutes for 8 hours (excitation wv – 485 nm, emission wv- 535 nm )(including shaking = aeration of the cultures 2 minutes prior each measurement)
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| - | =Our Team (WILL BE MOVED)= | + | |
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| | [[Image:Grouppicture.jpg|center|600px|The University of Sheffield Team]] | | [[Image:Grouppicture.jpg|center|600px|The University of Sheffield Team]] |
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| | From left to right: | | From left to right: |
| | * Oluwaseun Samuel Awotunde | | * Oluwaseun Samuel Awotunde |
| - | * Malgorzata Poczopko | + | * Malgorzata Poczopko - mba07mp@sheffield.ac.uk |
| | * Muhammad Hammad Karim | | * Muhammad Hammad Karim |
| - | * Eva Barkauskaite | + | * Eva Barkauskaite - mbb07eb@sheffield.ac.uk |
| | * Dmitry Malyshev | | * Dmitry Malyshev |
| - | * Rosie Bavage | + | * Rosie Bavage - mba07rb@sheffield.ac.uk |
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| - | =Lab Books=
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| - | <!-- Nasty HTML hack to get the gallery centred -->
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| - | <div align=center>
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| - | <gallery align=center perrow="3">
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| - | Image:Dmitry_shef.jpg|[[Team:University_of_Sheffield/Dimtry | Dimtry's Lab Book]]
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| - | Image:Eva_shef.jpg|[[Team:University_of_Sheffield/Eva | Eva's Lab Book]]
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| - | Image:Gosia_shef.jpg|[[Team:University_of_Sheffield/Gosia | Gosia's Lab Book]]
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| - | Image:Hammad_shef.jpg|[[Team:University_of_Sheffield/Hammad | Hammad's Lab Book]]
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| - | Image:Rosie_shef.jpg|[[Team:University_of_Sheffield/Rosie | Rosie's Lab Book]]
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| - | Image:SAM_shef.jpg|[[Team:University_of_Sheffield/Sam | Sam's Lab Book]]
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| - | </gallery>
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| - | </div>
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| - | =Timetable=
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| - | ===Dry Lab Period ===
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| - | '''February 2008'''
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| - | The very beginning. Three team members, Gosia, Eva and Dmitry met each other to discuss the possibility of joining iGEM competition this year. Straight after that Rosie joined the team.
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| - | March 2008 – The idea to participate in iGEM was presented in the Department of Molecular Biology and Biotechnology (MBB) in the students and staff committee meeting. The head of MBB Department, Prof. D. Hornby agreed to help us in managing this project.
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| - | '''April 2008'''
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| - | *The team now consisted of 9 members, mostly joined by MBB Level 2 students. The early brainstorming took place. However, no ideas that would be feasible to complete during the summer and would have actual impact on science appeared.
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| - | *A new science orientated society was established within the University of Sheffield Union of Students. The initial purpose of the SynBio society was to help students within the University to participate in iGEM next year, along with that a Scientific Journal Club with monthly meetings is on the agenda
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| - | * Applications of Funding to various sources were sent out.
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| - | '''June 2008'''
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| - | * the idea of sensing biological water contamination employing the Quorum Sensing mechanism was finalised
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| - | * 15th June - meeting with Prof. P. Wright took place to discuss a possibility to join labs in the Bioincubator, a new business and research facility in Sheffield
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| - | * 29th June - two level 2 students representing the Department of Automatic Control and Systems Engineering joined the team to cover the Engineering parts of the project.
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| - | * 30th June - meeting with Dr. Catherine Biggs from the ChELSI group took place to discuss a possible approach towards using the Quorum sensing as a way of sensing water contamination
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| - | '''July 2008'''
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| - | * 2nd to 16th July - team members representing biological and engineering sides of the project introduced each other to their plans of action as well as explained the material behind it.
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| - | * 7th July - meeting with Prof. Marian Gheorghe from Automatic Control and Systems Engineering. The meeting discussed the approach towards mathematical modeling of the Quorum Sensing using E.coli as a tool.
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| - | * iCHEME offered a financial contribution towards the trip to Jamboree.
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| - | * Discussions with the group as well as Dr. C. Biggs, with an aim to choose the right model organism to represent water pathogens.
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| - | * Ph.D. student Esther Karunakaran proposed using a fusion histidine kinase as a receptor for V. cholerae autoinducer . V. cholerae , one of the causative agents of water borne diseases, was then chosen as a model organism representing water pathogens.
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| - | * The native E.coli BarA - UvrY signal transduction pathway was selected for "hijacking" by our fusion kinase.
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| - | * 20th July - students discussed a possible target for GFP insertion in the E.coli genome, the pgaABCD operon was chosen.
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| - | * Prof. P. Wright and Dr. C. Biggs representing the ChELSI research group within the University of Sheffield approved the project plan and agreed to provide lab materials and lab space in the Bioincubator research facility.
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| - | * IDT DNA kindly agreed on a contribution of £1000 towards the cost of gene synthesis and primer orders. The CqsS – a native receptor for CAI-1 molecules was ordered for further experiments.
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| - | '''August 2008'''
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| - | * 4th August - meeting with David Wengraf to discuss possible biohazard before final approval to enter Bioincuabotr Labs.
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| - | * 4th and 5th August - meetings with Prof. Rice so as to choose a correct place to cut the CqsS and BarA to have a functional fusion kinase.
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| - | === Wet Lab Period ===
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| - | '''Mid - August 2008'''
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| - | * 7th August - team enters the labs to start actual experiments. Preparation for gene knockout using Datsenko and Wanner method takes place. Prof. Stafford from the Univeristy of Sheffield Medical School provides us with electroporation protocol. From 11th August to mid September the electroporation is carried out unsuccessfully.
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| - | * 15th August - an official project presentation to the ChELSI research group.
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| - | * the transformation using the Biobrick BBa_I763004 containing a plasmid with GFP – LVA tag is carried out. All attempts are unsuccseful despite using pre – approved protocols and cultures.
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| - | * 26th August - Mr. Peter Grant representing the Biofusion Group provides funding towards the costs of U. S. VISA.
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| - | '''September 2008'''
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| - | * The gene order for CqsS membrane receptor arrives.
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| - | * Along with that Prof. B. Bassler from Princeton University sends us the plasmid containing CqsA - a protein producing CAI -1 (Cholera Autoinducer – 1) with the purification protocol
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| - | * Prof. O. Melefor from Karolinska Instutue kindly sends us a DH5 – alpha strain containing a barA knockout
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| - | * Prof. Robert Poole agrees to provide further funding towards the trip to USA. On 16th September the hotels and flights to the Jamboree are booked, along with registration confirmation of all attending team members.
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| - | * The electroporation and transformation are still unsuccessful even after extensive troubleshooting.
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| - | * 29th September VISA is attained for all the students.
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| - | '''October 2008'''
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| - | * Plasmid prep of one possible GFP - LVA transformant colony is made. The attemts to characterize it using Tecan as well as loading restriction digest of the plasmid prep on an agarose gel suggests that the colony was most likely contamination.
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| - | * 8th to 15th October -preparation for Biobrick submission to the Parts Registry takes place. Failed transformations raise suspicions of a faulty Biobrick booklet. Thorough investigation of various DNA parts from all over the booklet proves this hypothesis. Due to faulty DNA shipment no parts can be submitted to the Registry.
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