Team:Kyoto/Project/Goal C
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===Experiment 1 Function check of SΔTMD1=== | ===Experiment 1 Function check of SΔTMD1=== | ||
====Bacterial strains==== | ====Bacterial strains==== | ||
- | We used | + | We used three types of E. coli, E. coli KRX transformed with <partinfo>BBa_K358021</partinfo>, KRX transformed with <partinfo>BBa_K358022</partinfo> and KRX transformed with <partinfo>BBa_K358024</partinfo>. |
- | [[Image:KyotoFigC001.png|450px]][[Image:KyotoFigC003.png|400px]] | + | [[Image:KyotoFigC001.png|450px]] |
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+ | [[Image:KyotoFigC003.png|400px]] | ||
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+ | dede | ||
====Measurement==== | ====Measurement==== | ||
We picked out three colonies from each devices, and cultivated them in M9 medium with 1mM IPTG and without IPTG overnight. Then, we measured A550 of each cultures. | We picked out three colonies from each devices, and cultivated them in M9 medium with 1mM IPTG and without IPTG overnight. Then, we measured A550 of each cultures. |
Revision as of 12:24, 26 October 2010
Contents |
Goal C: Characterization of the anti-killer gene
Introduction
we selected SΔTMD1 as anti-killer gene of Lysis box. Lysis cassette encodes S gene, R gene and so on and the transmembrane domein 1(TMD1) of this S gene is essential for the function of lysis cassette as killer-gene. So SΔTMD1, which is a S mutant with TMD1 deleted, dominant-negatively inhibits Lysis cassette.(check Learn more) That is why we selected SΔTMD1 as anti-killer gene.
Then, we checked if SΔTMD1 prevent Lysis cassette from causing the cell death. To research this function of SΔTMD1, we used the E.coli transformed with both these genes( <partinfo>BBa_K358021</partinfo>). Because E.coli is immediately dead if killer-gene is constitutively expressed, we made lysis cassette regulated by lac promoter. The E.coli were grown in the medium without IPTG, and after there were enough E.coli, they were cultured in the one with IPTG to express Lysis cassette. After that, we checked, by measuring the absorbance (OD600), if E.coli were alive due to anti-killer gene, SΔTMD1 expressed constitutively.
Experiment 1 Function check of SΔTMD1
Bacterial strains
We used three types of E. coli, E. coli KRX transformed with <partinfo>BBa_K358021</partinfo>, KRX transformed with <partinfo>BBa_K358022</partinfo> and KRX transformed with <partinfo>BBa_K358024</partinfo>. {{}} {{}} dede
Measurement
We picked out three colonies from each devices, and cultivated them in M9 medium with 1mM IPTG and without IPTG overnight. Then, we measured A550 of each cultures.