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| | =Introductory Lab Sessions= | | =Introductory Lab Sessions= |
| | [[Image:Team-Newcastle iGem 2009 - Lab 03-07-09 no 1.JPG|thumb|right| Jane and Jess calculating serial dilutions]] | | [[Image:Team-Newcastle iGem 2009 - Lab 03-07-09 no 1.JPG|thumb|right| Jane and Jess calculating serial dilutions]] |
| - | ==Lab rules==
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| - | * Always use the distilled water from the green tap
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| - | * Always label things at teh lab with the red tape. Put the initials, the lab name (PA), date and what is inside
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| - | * For anything needs to be autoclaved, use the specific marker and place it on top of the boxes/
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| - | * Clean the bench before and after the work
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| - | * Dry the cases before using them
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| - | * Keep a distilled water to use on the table
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| - | * No actual work after 5 or 6 pm - if the autoclaver is needed, the experiments requiring it should be presented to the operator by 4pm
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| - | ==The first week initial planning, 30 June - 3 July==
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| - | [[Image:Team Newcastle iGem 2009 - Lab 01-07-09 no 10.jpg|thumb|right| Shaking incubator]]
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| - | *Tuesday
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| - | # Find the strain
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| - | # Pour the plates (if necessary)
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| - | ##Cool the media to 10C
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| - | ##Dry them
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| - | #Get the strain from the freezer inoculate for Tuesday
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| - | #Prepare the solutions and the media
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| - | *Wednesday
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| - | #Plate-> Single colony 5ml LB-> 37C incubation for Thursday
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| - | *Thursday
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| - | #Preworm the media at 37C
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| - | #Sample->wash 2x-? Suspend in 1ml->freeze->-80C
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| - | *Friday
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| - | #Transformation test with a plasmid
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| - |
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| - | ==Lab session: 30th June==
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| - | *We got samples of E.coli DH2 Alpha strains and placed them into three plates. They are placed for incubation at 37C
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| - | *Glycerol concentration will need be chanegd as 50%
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| - | *We have created 0.1M of CaCl2 using 5.5 gram of CaCl2. The final solution is 0.5 liter. We placed them into 4 boxes (three 100ml and one 200ml). They have blue covers. We have left them for autoclaving.
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| - | * We prepared LB solution using 20gr LB. Th final volume is 1 liter. We put them into boxes and left for autoclaving.
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| - |
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| - |
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| - | ==Lab session: 1st July==
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| - | [[Image:Team Newcastle iGem 2009 - Lab 01-07-09 no 6.JPG|thumb|right|Jess streaking some agar plates]]
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| - | [[Image:Team Newcastle iGem 2009 - Lab 01-07-09 no 9.JPG|thumb|right|Jane applying aseptic technique]]
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| - | Things we need for today:
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| - | *LB
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| - | *Containers
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| - | *Sterile tubes
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| - | *Space in incubator for tonight
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| - |
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| - |
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| - | * We plated out single cultures from yesterday's plates for a practice.
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| - | * We inoculated 2ml of LB with single cultures from yesterday's plates and put them in the shaking incubator.
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| - | * We made up some 50% glycerol and it was sent to be autoclaved.
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| - |
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| - |
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| - | Things we need for tomorrow (Thursday):
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| - | *Have we used up a lot of anything- is there enough for Thursday?
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| - | #Sterile tubes
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| - | #Pipette tips
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| - | #Solutions
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| - |
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| - | Culture
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| - | #Sterile flasks for culture (500ml)
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| - | #Spectrophotometer and cuvettes (where)
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| - | #Arrange space in shaking incubator
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| - |
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| - |
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| - | Harvest cells
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| - | #Centrifuge/ centrifuge vial (200ml?)
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| - | #Ice bucket and ice
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| - | #Glycerol
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| - | #Sterile microfuge tubes
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| - | #Liquid nitrogen
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| - |
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| - |
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| - | ==Lab session: 2nd July==
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| - | [[Image:Team Newcastle iGem 2009 - Lab 02-07-09 no 1.JPG|thumb|right|James innoculating LB with pre-culture]]
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| - | * 1ml of preculture (which had been left overnight) was taken and used to inoculate 200ml of LB (standard bacterial broth). The flask which contained the mixture was then placed into the shaker, which both incubated the culture at 37 degrees Celsius and constantly shook the flask.
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| - |
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| - | * Once 2 hours had elapsed, the optical densities of the cultures were taken using a spectrophotometer. This was to determine whether the cells had grown and if they had, where the cells were in their growth phase. For competency, <i>E.coli</I> need to be in early log phase. The results were as follows:
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| - |
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| - |
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| - | {| border="1"
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| - | |-
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| - | ! Sample
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| - | ! Absorbance (nm)
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| - | |-
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| - | | 1
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| - | | 0.346
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| - | |-
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| - | | 2
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| - | | 0.443
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| - | |-
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| - | | 3
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| - | | 0.450
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| - | |}
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| - | * The next step was to transfer the three cultures into a centrifuge and allow them to spin for 10 minutes, at a speed of 8,000 rpm and at a temperature of 4 degrees celsius. Because balance is required in a centrifuge (i.e. even numbers), we only used two of the tubes.
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| - | [[Image:Team Newcastle iGem 2009 - Lab 02-07-09 no 3.JPG|thumb|right|Hanny preparing pre-culture sample]]
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| - |
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| - | * Once spun, the supernatant was removed and the pellet was resuspended in calcium chloride, which had been placed in a fridge since the solution was made. The concentration of the calcium chloride was 0.1M and the volume was 40ml.
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| - | * The cells emersed in the calcium chloride were then held in ice for 40 minutes.
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| - | * Once 40 minutes was complete, the cells were once again centrifuged at a speed of 8,000 rpm and at the temperature of 4 degrees celsius. After being spun, the supernatant was removed and the pellet was resuspended in 1ml calcium chloride again. This solution was again pre-chilled in the fridge, was again 0.1M but only 1ml was applied this time round.
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| - |
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| - | * 50% glycerol was then applied to the mixture. Because the concentration of the glycerol to cell mixture was supposed to be 10%, we applied 0.ml to 0.9ml of cell mixture.
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| - | * The resulting mixture was then placed into 50 microfuge tubes (each with a capacity of 100 microlitres) with these tubes being placed into a flask of liquid nitrogen. This process shock-freezes the <i>E.coli</I> cells.
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| - |
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| - | * After being given a few minutes to confirm freezing of the cells, the tubes were immediately scooped out of the flask and transferred immediately into a -80 degrees celsius freezer for storage.
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| - | ==Lab session: 3rd July==
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| - | [[Image:Team Newcastle iGem 2009 - Lab 03-07-09 no 2.JPG|thumb|right|Jane and Jess preparing serial dilutions]]
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| - | Today we were transforming DNA using Phil's protocol, however we used the following changes:
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| - |
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| - | * We added 3µl of DNA to our cells.
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| - | * We plated out 100µl of our dilutions.
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| - | * We incubated our transformed cells for the full 60 mins.
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| - | * We used the ampicillin resistance plasmid '435'
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| - |
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| - | ===Procedure===
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| - | * We followed the protocol using sterile technique where possible, as well as wearing gloves to prevent contamination of the DNA.
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| - | ** Glass tops such as LB jars can be run under the flame, however plastic eppendorfs cannot so working around the flame is sufficient.
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| - | * We found it easier if the person pipetting held the eppendorf as they can see what they're doing better.
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| - | * Prof. Aldridges lab uses sterile beads to plate ourt rather than plastic spreaders, these are a bit fiddly so it may take a while to get used to tipping the right amount out!!
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| - |
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| - | ===Our serial dilutions were prepared as follows:===
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| - | [[Image:Team Newcastle iGem 2009 - Lab 03-07-09 no 5.JPG|thumb|right|Spreading the diluted cells across the agar surface using sterile glass beads]]
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| - | * Using the waiting times within our procedure we set up 6 labelled eppendorf tubes with 900µl of LB, ready for the series dilution.
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| - | * We took 100µl of our incubated cells and put them in tube 1, mixed the solution briefly and then proceded to take 100µl of the diluted cells and tranfer them along the line of eppendorfs, resulting in eppendorfs containing 10-1 to 10-5 solutions for both the control and 'transformed' cells.
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| - | *We plated all 6 transformed ''E.coli'' solutions onto LB+amp agar plates, and the controls we plated onto both LB+amp plates(to check for contamination) as well as plain LB plates (in order to later calculate transformation frequency).
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| - | ==Lab session: 6th July==
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| - | [[Image:Team Newcastle iGem 2009 06-07-09 no 2.JPG|thumb|right| Goksel rehydrating the BioBricks, which are in dry DNA form]]
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| - | List of bricks for the day
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| - | #Bba_J04450 (plasmid:PSB1AK3). Location: Plate 1, Well 13A
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| - | # ? (plasmid:PSB1AK3). Location: Plate 2, Well 8A
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| - | #Bba_L13522 (plasmid:PSB1AT3). Location: Plate 1, Well 15A
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| - |
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| - | ===Preparation of the tubes===
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| - | * We got 3 tubes containing cells from the freezer at 80C and placed them into the ice and waited for 30 minutes
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| - | * We prepared 6 tubes (3 tubes for controls and 3 tubes for the plasmids) for the bricks
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| - | * We added 40ul of cells to each of the six tubes
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| - | * We added 3ul of DNA for the plasmid tubes and 3ul of water for the control tubes
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| - | * We added 900ul of LB for each of the six tubes
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| - | * We then placed the tubes in the shaking incubator for an hour.
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| - |
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| - | ===Plating out===
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| - | [[Image:Team Newcastle iGem 2009 06-07-09 no 7.JPG|thumb|right| James extracting portion of diluted solution to be placed on plates]]
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| - | [[Image:Team Newcastle iGem 2009 06-07-09 no 14.JPG|thumb|right| Hanny spreading solutions on plate using sterile glass beads]]
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| - | We prepared 9 plates with full strength (undiluted) and 9 plates with diluted tube content.
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| - |
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| - | ;Plates with undiluted content
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| - | *The first three plates having LB + Amp were used as the negative control. Hence the cells not having amp. resistance would not grow on these plates.
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| - | * The next three plates with LB content were used as the positive control. Cells without amp. resistanec would still grow on these plates.
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| - | * The other three plates were used for the plasmids.
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| - |
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| - | {| class="wikitable" border="1"
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| - | |-
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| - | | LB + Amp, (-) control 1
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| - | | LB, (+) control 1
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| - | | LB + Amp, Transformation Plasmid 1
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| - | |-
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| - | | LB + Amp, (-) control 2
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| - | | LB, (+) control 2
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| - | | LB + Amp, Transformation Plasmid 2
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| - | |-
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| - | | LB + Amp, (-) control 3
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| - | | LB, (+) control 3
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| - | | LB + Amp, Transformation Plasmid 3
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| - | |-
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| - | |}
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| - |
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| - |
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| - | ;Plates with diluted content
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| - | * For the diluted ones we used 900ul of LB and 100ul of DNA from the corresponding tubes.
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| - | * The same set of 9 plates were prepared for the diluted content.
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| - | <br>
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| - | ==Lab Session:7th July==
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| - | <b>Experiment summary so far...</b> Yesterday, we attempted to transform cultures with BioBricks. We inserted the three BioBricks into competent <i>E.coli</i> cells grown in the previous lab session (via plasmids) and grew them overnight. The cells were spread on plates in both undiluted and diluted forms. The diluted solution of competent <i>E.coli</i> cells were spread onto three different plates - a negative control plate, a positive control plate and a plasmid plate (see table above). Today we reviewed the cultures which grew on the plates and prepared them for plasmid extraction and purification - this will form tomorrow's experiment.
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| | <br> | | <br> |
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| - | <b>Observations</b>
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| - | Firstly, none of the <i>E.coli</i> cells mixed with BioBrick 1 (in the presence of competence inducers) took up the DNA - they didn't appear on the diluted or undiluted plates, which were lined with ampicillin. However the <i>E.coli</i> cells which had been mixed with BioBricks 2 and 3 did take up the DNA as they were present in colonies on ampicillin-covered plates. There were two colonies of bacteria which had been transformed by BioBrick 2, and eight colonies transformed by BioBrick 3. These 10 cultures became the focus of the subsequent experiments.
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| - | <br>
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| - | <b> Preparation of Solutions</b>
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| - | To prove that the DNA the <i>E.coli</i> cells had taken up really was the BioBrick added to the solution, we need to carry out the procedure of DNA electrophoresis with the aid of restriction enzymes. In order to carry out this step, we need to extract and purify the plasmids first (to be done tomorrow) via alkaline lysis - this requires three solutions, two of which were made today.
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| - | <br>
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| - | <u>Solution 1</u>
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| - | <br>
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| - | According to Dr. Aldridge's protocol named "Phil’s mini method for Alkaline Lysis for Mini Prep", we need to add 'solution 1' (along with an RNAse) to resuspended transformed ''E.coli'' cells. Solution 1 required the following ingredients at the following concentrations:
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| - | * 50 mM Glucose
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| - | * 25 mM Tris.Hcl (pH 8.0)
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| - | * 10 mM EDTA (pH 8.0)
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| - | This solution was made today in preparation for tomorrow's exercise. We were told that the total volume should be 250ml. We were presented with pre-made solutions - 1M Tris HCl and 0.5M EDTA - and were told we needed to calculate the correct volumes of each of these solutions to be added to the beaker to give the desired molarity. We were presented with glucose in it's solid form and asked to make a stock solution of 1M glucose; after which we were asked to calculate the amount to glucose solution to add to the beaker to make a molarity of 0.5M! The following equation helped:
| + | *[https://2009.igem.org/Team:Newcastle/Project/Labwork/Week1/Week1 Introductory Lab Sessions] (30th June - 3rd July 2009) |
| - | <br>
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| - | Molecular Weight x Desired Volume (Litres) x Molarity = Weight (grams)
| + | *[https://2009.igem.org/Team:Newcastle/Project/Labwork/Week1/Week2 Introductory Lab Sessions] (6th July - 10th July 2009) |
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| - | Solution I (can be stored at RT until Rnase A added)
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| - | * 50 mM Glucose
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| - | * 25 mM Tris.Hcl (pH 8.0)
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| - | * 10 mM EDTA (pH 8.0)
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| - | you can make it up to 500 ml
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| - | Add 250 ul of RNase A to 50 ml of Sol. I then store at 4°C
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| - | Solution III (for 100 ml)
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| - | * 5M Potassium acetate: 60ml
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| - | * glacial acetic acid: 11.5 ml
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| - | * H2O: 28.5 ml
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| - | <u>Solution 3</u>
| + | *[https://2009.igem.org/Team:Newcastle/Project/Labwork/Week1/Week3 Introductory Lab Sessions] (14th July - 17th July 2009) |
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| | + | *[https://2009.igem.org/Team:Newcastle/Project/Labwork/Week1/Week4 Introductory Lab Sessions] (23rd July - 24th July 2009) |
| | {{:Team:Newcastle/Footer}} | | {{:Team:Newcastle/Footer}} |
| | {{:Team:Newcastle/Right}} | | {{:Team:Newcastle/Right}} |
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