Team:Kyoto/Project/Goal C

From 2010.igem.org

(Difference between revisions)
(Bacterial strains)
m (Goal C: Characterization of the anti-killer gene)
Line 2: Line 2:
==Goal C: Characterization of the anti-killer gene==
==Goal C: Characterization of the anti-killer gene==
===Introduction===
===Introduction===
-
we selected SΔTMD1 as anti-killer gene of Lysis box.  
+
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.
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 [[Team:Kyoto/LearnMore#Lysis Cassette|Learn more]])
So SΔTMD1, which is a S mutant with TMD1 deleted, dominant-negatively inhibits Lysis cassette.(check [[Team:Kyoto/LearnMore#Lysis Cassette|Learn more]])
Line 21: Line 21:
====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 culture.

Revision as of 14:05, 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>. KyotoFigC001.pngKyotoFigC003.png

  • BBa_K358021:Anti-killergene is induced constitutively and killergene is regulated by lactose promoter.
  • BBa_K358022:lacP + SΔTMD1RRz, TMD1 is deleted from lysis cassette[SRRz].
  • BBa_K358024:This part is the same to BBa_K358021, except for its constitutive promoter[BBa_J23101]. So, this part also induces constitutively SΔTMD1 gene, the anti-killer gene, and lambda lysis cassette[SRRz], the killer gene, is regulated by lacP.

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 culture.


Result

Result

Discussion