Caltech/Project/N
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==Role in Lambda Life Cycle== | ==Role in Lambda Life Cycle== | ||
- | PL and PR are the first promoters activated during λ infection. N is transcribed from PL, so it acts early in the phage’s developmental cycle. | + | PL and PR are the first promoters activated during λ infection. N is transcribed from PL, so it acts early in the phage’s developmental cycle. N is necessary to transcribe genes necessary for both lysis and lysogeny. In the absence of N, the phage cannot go into either pathway and it will not be infectious. |
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==Original Goals== | ==Original Goals== | ||
- | The objective of this subproject project was to determine the necessary concentration of N protein required for lysis. The N gene was placed behind a tetracycline-inducible promoter in a low copy (pSB2K3) plasmid. Addition of anhydrotetracycline (aTc) would induce the production of N. For more details, please see our list of constructs [[Caltech/Project/Constructs|here]. This construct was transformed into D1210 ''E. coli'' and titered using N amber mutant phage. | + | The objective of this subproject project was to determine the necessary concentration of N protein required for lysis. The N gene was placed behind a tetracycline-inducible promoter in a low copy (pSB2K3) plasmid. Addition of anhydrotetracycline (aTc) would induce the production of N. For more details, please see our list of constructs [[Caltech/Project/Constructs|here]]. This construct was transformed into D1210 ''E. coli'' and titered using N amber mutant phage. |
==Status and Future Plans== | ==Status and Future Plans== | ||
- | + | [[Image:N_results.jpg|center|frame|Results of titering N amber mutant phage on D1210 containing the tet-regulated N construct.]] | |
==Relevant Protocols== | ==Relevant Protocols== | ||
* [[Caltech/Protocols/Titering | Titering]] | * [[Caltech/Protocols/Titering | Titering]] | ||
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</div> | </div> |
Latest revision as of 03:52, 27 October 2007
iGEM 2007
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