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Revision as of 13:30, 26 October 2010 (view source) Ptmvanboheemen (Talk | contribs) (→RBS Characterizaton) ← Older edit		Revision as of 13:33, 26 October 2010 (view source) Ptmvanboheemen (Talk | contribs) (→Hydrocarbon & Salt Tolerance) Newer edit →
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	===Hydrocarbon & Salt Tolerance===		===Hydrocarbon & Salt Tolerance===
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	===Solubility===		===Solubility===
	[[Image:TU_Delft_BioBrick-formation-emulsifier.png]]		[[Image:TU_Delft_BioBrick-formation-emulsifier.png]]

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Revision as of 13:33, 26 October 2010

Cloning Plan

Once we decided what we wanted to achieve and with which genes, we designed the following cloning plan.

At the start of our project we tried to perform [http://partsregistry.org/Assembly:3A_Assembly| three-way ligation] as describe in the part registry. Because we experienced troubles by ligating small parts. We used a different approach to make our BioBricks by performing two-way ligation.

Two-way ligations strategies

By using two-way ligation we ligated two parts to each other. The backbone of the smallest part was cut open. The largest part was cut out of its backbone. Then both parts were mixed and ligated. To prevent self-ligation we cut the backbone with an additional restriction enzyme.

Cloning strategy A

In the case when the smallest part had to be downstream of the largest part, we used cloning strategy A

The smallest brick (blue) was cut with EcoRI and XbaI

The largest brick (orange) was cut with EcoRI and SpeI

It is important that the additional enzyme only cuts in the backbone and not in the part itself

Cloning strategy B

In the case when the smallest part had to be upstream of the largest part, we used cloning strategy B

The smallest brick (green) was cut with SpeI and PstI

The largest part (blue) was cut with XbaI, PstI

It is important that the extra enzyme only cuts in the backbone and not in the part itself

Cloning strategy C

In the end all BioBricks have to be cloned in the pSB1C3 plasmid backbone. With our strategy all the BioBricks are still in its original plasmid backbone, which in most cases was pSB1A2. We performed a pSB1C3 migration which is illustrated by cloning strategy C.

The part (blue) was cut with EcoI and PstI

To prevent self-ligation we cut the backbone with an additional restriction enzyme. It is important that the extra enzyme only cuts in the backbone and not in the part itself.

The vector backbone (brown) was cut with EcoRI, PstI

To prevent self-ligation we cut the insert with an additional restriction enzyme. In the case of the iGEM vectors is the insert J04450. It is important that the extra enzyme only cuts in the insert and not in the part itself.

Our plan

Our BioBricks are build from multiple parts. To make the final BioBrick several intermediates had to be prepared. Here our complete cloning plan of the different sub projects are illustrated.

Alkane Degradation

Hydrocarbon & Salt Tolerance

Solubility

Sensing

RBS Characterizaton