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| Yeast promoter sequences of varying strength have been provided for our work. The following are the available promoters: | | Yeast promoter sequences of varying strength have been provided for our work. The following are the available promoters: |
| {| style="margin-left: 70px;" | | {| style="margin-left: 70px;" |
- | !width="100"|ARD1p | + | !width="100"|[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530016 RPS8Bp] |
| !width="100"|[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530005 BAP2p] | | !width="100"|[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530005 BAP2p] |
| !width="100"|[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530015 FCY2p] | | !width="100"|[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530015 FCY2p] |
Line 29: |
Line 29: |
| !width="100"|[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530010 HHO1p] | | !width="100"|[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530010 HHO1p] |
| |- | | |- |
- | |'''[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530003 KRE9p]''' ||'''[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530007 PRY1p]''' ||'''RPL8Ap''' ||'''RPL24Ap''' || '''[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530009 RPS2p]''' | + | |'''[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530003 KRE9p]''' ||'''[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530007 PRY1p]''' ||'''[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530004 STM1p]''' ||'''[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530008 TDH3p]''' || '''[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530009 RPS2p]''' |
- | |- | + | |
- | |'''[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530016 RPS8Bp]''' || '''[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530004 STM1p]''' || '''[http://partsregistry.org/wiki/index.php?title=Part:BBa_K530008 TDH3p]''' || | + | |
| |} | | |} |
| | | |
Promoters and UTRs
As we began our work with Saccharomyces cerevisiae, it came to our attention that the database is deficient in genes for this organism. This deficiency is due in part to the fact that E. coli genes are widespread through the database, whereas yeast remains a largely untapped area. In order to address this problem and facilitate the use of yeast in synthetic biology we have decided to provide the basic parts required for gene use and assembly. Dr. Jef Boeke has provided some basic parts including promoters and termination sequences of varying strengths. This will allow future teams the ease of use of premade biobricked sequences to use with their genes.
Promoters
Yeast promoter sequences of varying strength have been provided for our work. The following are the available promoters:
UTRs
Similarly, the following UTRs, or termination sequences have been provided for our work: