Team:SDU-Denmark/Notebook

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===Create biobrick RIP+Export in registry===
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Revision as of 08:47, 9 July 2009

Home The Team The Project Parts Submitted to the Registry Modeling Notebook


Contents

Project task-management notebook

Todo

Create biobrick RIP in registry

Create biobrick RIP+Export in registry

Doing

Plasmid backbone

Task: Find a backbone for both e.coli and b. subtilis

Status: Doing.

People: Helle and Mike

Last edit: July 8th 2009.

July 7th 2009: We found the backbone, [http://partsregistry.org/wiki/index.php/Part:BBa_I742123 BBa_I742123], which other teams have found to be compatible with both both gram positive and gram negative bacteria, such as e. coli.

After talking to HQ, it turns out that the quality of their stock is bad, and they will try to get some home from older teams. Furthermore, it might simply be better to use a more specifik backbone for e. coli and for b. subtilis.

(mike)


July 8th 2009: We decided to start working with [http://partsregistry.org/Part:pSB1A3 pSB1A3] instead, which is a high-output e. coli backbone.

Output: 100-300 number pr. cell. Resistance: ampicillin (we're going with 50 µg/mL first)

(mike)

Inducible promoter

Task: Find a promoter, that can be induced

Status: Doing.

People: Anna

Last edit: July 8th 2009.


July 7th 2009

I found the inducible promoter BBa_R0011 that is regulated by LacI.

It is a strong promoter, that will be on in stains without LacI.

(anna)


E. coli strain

Task: Find a e.coli strain

Status: Doing.

People:

Last edit: July 8th 2009.

July 7th 2009

The plasmid seems to be working in most types (no need for ccdB) Jacob suggests E. coli KG22, which can turns on the operon by adding IPTG.

July 8th 2009

We'll use Top10 e.coli strain


Done

Done Done