Team:UCL London/Characterisation

From 2010.igem.org

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The 3 parts were innoculated into seperate 1 L fermenters and we ran the processes in parraellel along side a control process. We observed the various stages of the process from the growth to the lag phase, and what we hoped to observe was the progressive change of the colours of the 3 processes into green, as we expected the induction of the GFP protein on addition IPTG causing the induction of the promoter and thus the green proteins release into the culture.
The 3 parts were innoculated into seperate 1 L fermenters and we ran the processes in parraellel along side a control process. We observed the various stages of the process from the growth to the lag phase, and what we hoped to observe was the progressive change of the colours of the 3 processes into green, as we expected the induction of the GFP protein on addition IPTG causing the induction of the promoter and thus the green proteins release into the culture.
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[[Image:MNARK Infors 02.jpg|400px|right]]
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[[Image:MNARK Infors 03.jpg|400px|right]]
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Revision as of 19:27, 24 October 2010

UCL IGEM 2010

RETURN TO IGEM 2010

1. CHARACTERISATION OF NEW PARTS

UCL-XIANGCHARAC1.JPG


Our pTAC with RFP reporter was characterised at lab scale by carrying out a successful transformation with a control. By adding transforming the parts into competent cells and adding IPTG to the non-control plate, we expected to see the control's colour remain unchanged whilst that of the other plate to turn red indicating that the IPTG will have induced the activation of the pTAC and thus characterise our part. Obviously, we had hoped to be in a position to characterise the whole genetic circuit but due to time restraints we could complete our circuit.



Check out our parts page to see the parts submitted in more detail [http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2010&group=UCL_London&Done=1|UCL_London 2010 iGEM Team Parts].

2. CHARACTERISATION OF EXISTING PARTS/DEVICES AT 1 L FERMENTER SCALE

As part of the Gold criteria which is our target, we had to characterise an existing part, and so we decided to characterise 3 devices from our 2009 parts;

[http://partsregistry.org/wiki/index.php?title=Part:BBa_K239011 UCL_London 2009 iGEM BBa_K239011 PART]

[http://partsregistry.org/wiki/index.php?title=Part:BBa_K239009 UCL_London 2009 iGEM BBa_K239009 PART]

[http://partsregistry.org/wiki/index.php?title=Part:BBa_K239015 UCL_London 2009 iGEM BBa_K239015 PART]


The 3 parts were innoculated into seperate 1 L fermenters and we ran the processes in parraellel along side a control process. We observed the various stages of the process from the growth to the lag phase, and what we hoped to observe was the progressive change of the colours of the 3 processes into green, as we expected the induction of the GFP protein on addition IPTG causing the induction of the promoter and thus the green proteins release into the culture.

MNARK Infors 05.jpg




MNARK IGEM plus control 02.jpg
MNARK IGEM plus control 03.jpg
MNARK Infors 02.jpg
MNARK Infors 03.jpg
UCL-Green.jpg
MNARK Infors 06.jpg
Time
45092
17481
11526

OXYGEN SUPPLY SWITCHED BACK ON

35924
20049
8382


Time
46577
18826
12078

OXYGEN SUPPLY SWITCHED BACK ON

38756
21730
8660
 

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