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Team:Leicester/Project
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===== Day Four ===== | ===== Day Four ===== | ||
(10:00 am) Started looking at the colonies and taking photos until the camera died after 11. The other 16 will have to wait until later. | (10:00 am) Started looking at the colonies and taking photos until the camera died after 11. The other 16 will have to wait until later. | ||
| + | (13:00) finished photographing all colony plates as found new camera. The next stage to make new plates which have polystyrene as the sole carbon source in an attempt to isolate the micorbes from our normal agar colonies that use polystyrene, its a way of purifying our colonies. This may take a while for the colonies to grow so our computer scientist, emily, will run simulations of what the degredation would look like over a period of time that exceeds the running time of our project. the new plates consist of a very small amount of agar so that when this carbon source runs out they switch to the expanded polystyrene which we have melted with acteone to produce a NON NEWTONIAN LIQUID that we will mix with the agar to produce a enriched form of agar. To maintain the liqiud state of the polystyrene we will use the orbital shaker provided by heathrow scientific for which we are very grateful. The measure of the petri dish are 17 ml agar at concentration..... and 3 ml liquid polysyrene (making 15% of the volume of the the overall solution). We will perhaps run this at different concentrations of liquid polystyrene of the overall volume 1%,5,10% and 15% to see what the best results will be and narrow down to the ideal concentration of polystyrene for our experiment to run optimally. | ||
=== The next step === | === The next step === | ||
== Results == | == Results == | ||
Revision as of 12:26, 12 July 2012
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Overall project
Our project is about trying to reduce the waste going to landfill by engineering a bacteria to degrade polystyrene. Some bacteria have been found to form biofilms on polystyrene, indicating that polystyrene may be being degraded. We have several different parts to our project, including a citizen science experiment (CSE).
We intend to extract the genes involved in any pathway degrading Expanded Polystyrene (EPS), and/or develop a new pathway involving modifications to existing enzymes able to degrade aromatic and aliphatic hydrocarbons to fit polystyrene and its derivatives into the active sites. The bacteria strain that we insert these new genes into should then be able to degrade polystyrene at a higher rate than natural bacteria, and future iGEM projects at the University of Leicester could harness this bacterial strain to produce useful products.
Project Details
The Citizen Science Experiment
The CSE was used to get the public involved in trying to find bacteria that could live on, and degrade expanded polystyrene (EPS). We asked them to bury a strip of EPS in the ground and leave it for a length of time (around 2 months), to find out whether bacteria might establish colonies, thus indicating that a colony could at the very least bind to, and possibly degrade EPS. The kits were Risk Assessed, and a copy of the assessment was included in the kit, along with instructions, a strip of EPS, and a self seal bag to put the EPS into. This was all contained in a stamped, addressed envelope at a cost to the public of £2 (+50p postage if bought online via our blog to cover the cost of sending the kit to the person). We recently had our first batch of kits back, ready to analyse.
The hope is that we'll find a bacteria that has been using polystyrene as a carbon source, so we can extract the genes responsible and attach them to high expression promoters to increase the amount of protein each bacterium produces. We will also be trying mutagenesis on these bacteria to increase the rate of reaction of the enzymes involved in the pathway.
The Experiments
Plating out the returned Citizen Science Experiment kits
The protocol
The first part involves halving the expanded polystyrene (EPS) lengthways with sterilized scissors in our returned citizen science experiment (CSE) kits so that we'll still have some of each sample left should we need it. First we need to do a practice with unused EPS strips (control and test). Pour/pipette 20ml LB agar into a petri dish and allow to set. Put line down middle in permanent marker USING A RULER! Then label one side swab (for the swabbing/scraping material) and the other side strip for the EPS strip (can use other names if you prefer). Add 50 micro litres of PBS (phosphate buffered saline) to each side of the half strip of EPS and scrape with spreader, before spreading onto the left half of the agar (or side labeled as 'swab'). Try to swab any mud off the strip if possible. Then place the half strip in the centre of the other half labeled 'strip'. Leave for a week at room temperature on the lab bench and examine agar for colonies. The other half of the strip should be put back into cold storage for future use.
Day One
Luke determines the protocol after much discussion with Dr B, Will and Tony, and we practice with unsterilised petri dishes, after getting everything we need to plate out samples.
Day Two
(10:30 am) continuation of agar plating. As well as running a few practises to ensure our technique is correct we have 25 CE kits to get through, in addition to a few controls using sterile polystyrene not placed in soil so to set a base line to compare our results too, you can never have too many controls. So as you can imagine it might take a while for us all to plate them, but it will be a big step to take on the road to our project success. (11:15 am) the production line begins, tony separating the petri dishes and luke plating out, will updating wiki as they go plus twittering, facebooking and other media communications, enjoy my sporadic posts.
(13:45 pm) Lab inductions complete and everyone can now be in the lab... yay. So on with the plating. 10 down 25 to go, luke working with Reema (our new member specialising in organic chemistry... now currently learning biology of plating). (14:45) 7 kits down, 18 to go Chris has taken over from Luke (who's writing this). The plated out kits are being left on a shelf by the bench. (17:00) Finished plating out the last of the 25. A good days work. Now we can leave the plates to grow cultures and see what we get.
Day Four
(10:00 am) Started looking at the colonies and taking photos until the camera died after 11. The other 16 will have to wait until later. (13:00) finished photographing all colony plates as found new camera. The next stage to make new plates which have polystyrene as the sole carbon source in an attempt to isolate the micorbes from our normal agar colonies that use polystyrene, its a way of purifying our colonies. This may take a while for the colonies to grow so our computer scientist, emily, will run simulations of what the degredation would look like over a period of time that exceeds the running time of our project. the new plates consist of a very small amount of agar so that when this carbon source runs out they switch to the expanded polystyrene which we have melted with acteone to produce a NON NEWTONIAN LIQUID that we will mix with the agar to produce a enriched form of agar. To maintain the liqiud state of the polystyrene we will use the orbital shaker provided by heathrow scientific for which we are very grateful. The measure of the petri dish are 17 ml agar at concentration..... and 3 ml liquid polysyrene (making 15% of the volume of the the overall solution). We will perhaps run this at different concentrations of liquid polystyrene of the overall volume 1%,5,10% and 15% to see what the best results will be and narrow down to the ideal concentration of polystyrene for our experiment to run optimally.
