THE PROJECT

ABSTRACT

In order to detect the presence of a specific non-natural amino acid (nnAA) in vivo the concept of amber suppression is used. This means the occurrence of the amber stop codon (UAG) in an open reading frame does not cancel protein translation but codes for a specific nnAA, in our case O-methyl-l-tyrosine (OMT). However, the incorporation requires the presence of the nnAA in the medium, otherwise the translation stops. The mechanism requires a tRNA with an anticodon complementary to the amber stop codon and an aminoacyl RNA synthetase (aaRS) loading the tRNA with the specific nnAA. The tRNA and aaRS combination is called an 'orthogonal pair'.

ABSTRACT

Glow before you go - What does this actually mean? The aim of our project is to make biology safer by introducing a suicide system into E. coli. Before the suicide is triggered, a reporter protein is expressed to indicate the release of E. coli or to show a deficiency of the non-natural amino acid in the surrounding medium which is necessary for the bacteria to survive. As a reporter protein, we chose mVenus which is a mutant of eYFP. mVenus is located downstream of a promoter which is repressed by a dimeric protein, the Zif23-GCN4 repressor. This repressor carries an amber mutation at position 4 (F4OMT). As a result, the non-natural amino acid O-methyl-l-tyrosine (OMT) is integrated into the protein sequence as long as there is enough OMT in the medium. With decreasing OMT concentration, the translation of the repressor stops due to the early amber stop codon and the repressor cannot bind to the promoter anymore. This leads to expression of the reporter protein mVenus which can be detected by fluorescence measurements.

ABSTRACT

Synthetic suicide systems have been chosen safeguards in synthetic biology since the field exists. There are different kinds of designs, often based on a regulating mechanism and a host killing toxin or different kinds of inhibitation of metabolic pathways. However, these most often do not tackle the problem of synthetic DNA surviving the death of host cells.
Here we show a possible design for a simple synthetic killswitch based on the endonuclease Colicin E2 and its corresponding suppressing protein Im2. Endonuclease and suppression protein expression is regulated by amber suppression. Therefore an amber stop codon coding for the non-natural amino acid O-methyl-l-tyrosine is implemented into the gene. The aim of the system is not simply killing the host, but also degrading all DNA within the cell and its surroundings, preventing the escape of transgenic DNA.

ABSTRACT

Artificial plasmids are a significant burden to the host. The design of pathways, e.g. the combination of different promoter and RBS systems, results in different amounts of product. Measurement of the metabolic burden is a key for quantitative optimization of metabolic engineering approaches. We want to establish a new approach to iGEM by providing a measurement strain to the community. As described by F. Ceroni et al., we integrated one copy of the GFP gene into the genom of E. coli, which offers us a highly accurate and instantaneous measurement of the impact of our plasmids on the host. Metabolic burden measurement is of economical interest, because it enables academic and industrial research testing several different pathways at once in a short time by using microplate reader. For the integration we used the λ‑Integrase site‑specific recombination pathway, described by A. Landy in 2015. Therefore, we designed two plasmids (BBa_K1976000 and BBa_K1976001) and measured them using single cell measurement and via microplate reader.

ABSTRACT

Since non‑inatural amino acids are expensive in comparison to natural amino acids we searched for a high yield synthesis method for O-methyl-l-tyrosine. Problems with chemical alterations of amino acids to form non‑natural derivates often lie in the higher reactivity of amino and carboxyl groups compared to other reactive groups. For this reason both groups need to be kept in mind while searching for a possible reaction for the desired synthesis.
For the protection of the amino group an acetylation reaction was carried out to form N‑acetyl‑L‑tyrosine. The tested method used N‑acetyl‑L‑tyrosine as a reagent which was then methylated at the carboxyl group and at the hydroxyl group using dimethyl sulfate by Williamson ether synthesis. To finally form the non‑natural amino acid, an acidic hydrolysis using hydrochloric acid was performed.