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Team:Todai-Tokyo/Notebook/bread
From 2009.igem.org
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=='''9/22'''== | =='''9/22'''== | ||
*read the sequence of mtlD→successful<BR> | *read the sequence of mtlD→successful<BR> | ||
| + | *mtlD primers with HAtag come<BR> | ||
| - | =='''9/ | + | =='''9/25'''== |
| + | *PCR of mtlD with new primer→failed<BR> | ||
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| + | =='''9/26'''== | ||
| + | *PCR of mtlD with new primer→successful<BR> | ||
| + | |||
| + | =='''9/27'''== | ||
*PCR of gpd1 promoter with Pfu Ultra<BR> | *PCR of gpd1 promoter with Pfu Ultra<BR> | ||
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=='''October'''== | =='''October'''== | ||
Revision as of 03:59, 14 October 2009
| Home | The Team | The Project | Parts Submitted to the Registry | Modeling | Notebook | Protocols | Ethics |
|---|
Contents |
Plan
Aim:Create yeast that can be used to make sweet and low energy bread
Methods:
- Clone the glucoamylase gene from Saccharomycopsis fibuligera
- Clone mtlD (mannitol synthase) from E.coli and insert it in the yeast chromosome by homologous recombination
- Replace gpd gene by mtlD
~9/20
- PCR of mtlD
- PCR of gpd1 promoter
- TA cloning of mtlD
"'9/21
- Miniprep of mtlD
9/22
- read the sequence of mtlD→successful
- mtlD primers with HAtag come
9/25
- PCR of mtlD with new primer→failed
9/26
- PCR of mtlD with new primer→successful
9/27
- PCR of gpd1 promoter with Pfu Ultra
October
- PCR of Glu1
- TA cloning of Glu1
- cut mtlD by XbaI and PstI
- PCR of gpd1 promoter with ExTaq
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