Team:Paris Saclay/Project/Odor-free ecoli

From 2014.igem.org

(Difference between revisions)
(The Principle of the construction)
(The Principle of the construction)
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In the lab, we already had a strain in which the tnaA was replaced by a kanamycin resistance, but this strain was too modified to be used for our project. So we switched the tnaA sequence with the kanamycin resistance in our bacterium by phage transduction. Transduction is the transfer of bacterial DNA from one bacterium (the donor) to another (the recipient) by a bacteriophage P1.
In the lab, we already had a strain in which the tnaA was replaced by a kanamycin resistance, but this strain was too modified to be used for our project. So we switched the tnaA sequence with the kanamycin resistance in our bacterium by phage transduction. Transduction is the transfer of bacterial DNA from one bacterium (the donor) to another (the recipient) by a bacteriophage P1.
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At first, the modified bacteria (cell donor) are infected by P1 phage. Transducing bacteriophage particles are formed in the donor bacterial cells during the phage growth. The bacterial chromosome is broken up into small fragments (approximately the same length as the P1 DNA). The phage particles mistakenly incorporate a piece of the bacterial DNA in place of phage DNA.
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At first, the modified bacteria (cell donor) are infected by P1 phage. Transducing bacteriophage particles are formed in the donor bacterial cells during the phage growth. The bacterial chromosome is broken up into small fragments (approximately the same length as the P1 DNA). The phage particles mistakenly incorporate the kanamycin resistance from the donor in place of phage DNA.
After the recombination, we used a flipase to delete the kanamycin resistance. The remaining bacterium doesn't smell at all.
After the recombination, we used a flipase to delete the kanamycin resistance. The remaining bacterium doesn't smell at all.

Revision as of 18:11, 7 October 2014

Contents

Countdown

This page is under Romain's responsibility

  • Deadline: 08/oct.
    • Completed text.
  • Deadline: 12/oct
    • Final review Philipe.

Odor-free E.coli chassis

Introduction

Escherichia coli stinks because of the tnaA gene which produces an enzyme that transforms the L-tryptophan into indole, responsible for the stench. If we want our lemon to smell like one, we have to delete this gene.

IndoleFormation.jpg

The Principle of the construction

In the lab, we already had a strain in which the tnaA was replaced by a kanamycin resistance, but this strain was too modified to be used for our project. So we switched the tnaA sequence with the kanamycin resistance in our bacterium by phage transduction. Transduction is the transfer of bacterial DNA from one bacterium (the donor) to another (the recipient) by a bacteriophage P1.

At first, the modified bacteria (cell donor) are infected by P1 phage. Transducing bacteriophage particles are formed in the donor bacterial cells during the phage growth. The bacterial chromosome is broken up into small fragments (approximately the same length as the P1 DNA). The phage particles mistakenly incorporate the kanamycin resistance from the donor in place of phage DNA.

After the recombination, we used a flipase to delete the kanamycin resistance. The remaining bacterium doesn't smell at all.

Paris Saclay Odor Free coli.jpg