Team:Johns Hopkins/Project/VitC

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======Introduction======
 
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As we begin our work with Saccharomyces Cerevisiae, it has come 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. The 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.
 
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======Promoters======
 
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Yeast promoter sequences of varying strength have been provided for our work. The following are the available promoters:
 
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ARD1p,
 
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BAP2p,
 
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FCY2p,
 
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Gal 1/10p,
 
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HHO1p,
 
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KRE9p,
 
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PRY1p,
 
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RPL8Ap,
 
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RPL24Ap,
 
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RPS2p,
 
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RPS8Bp,
 
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STM1p,
 
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TDH3p
 
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======UTRs======
 
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Similarly, the following UTRs, or termination sequences have been provided for our work:
 
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ARD1utr,
 
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BAP2utr,
 
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FCY2utr,
 
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HHo1utr,
 
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KRE9utr,
 
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PRY1utr,
 
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RPL8Autr,
 
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RPL24Autr,
 
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RPS2utr,
 
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RPS8Butr,
 
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STM1utr,
 
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TDH3utr
 
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Revision as of 23:02, 19 September 2011

VitaYeast - Johns Hopkins University, iGEM 2011