Team:Alberta/Parts
From 2012.igem.org
|
The parts we have made are composed of protein generating open reading frames, ribosomal binding sites, promoters, and copy-number controlled vectors. We describe each of these classes of part in turn.
<groupparts>iGEM012 Alberta</groupparts>
We have made and tested parts for producing colors and repressors. The color proteins are red, based on E1010, yellow, based on amilGFP K592010, and blue, based on amilCP K592009. Repressor proteins are lambda CI, LacI, and TetR, based on C0051, C0012, and C0040 respectively. The sequences are unmodified except for removal of restriction sites, removal of degradation tags, and replacement of stop codons. The sequences were synthesized along with their RBSes.
Our original intent was to create a series of RBS sequences of similar
strength that were each tailored to a particular ORF, and that showed
significant sequence variation between each other to minimize the chances of
intra-molecular recombination when used in combination. We used the online
Salis RBS calculator (Salis et al, Nat Biotech 27: 946 2009) to calculate RBSes for each protein coding sequence with a target translation initiation strength set to a value of 50,000 for each of
the ORFs shown above using a common length constraint that began with the
common transcriptional start site (position -1 of the common promoter
downstream region- Fig.1 below). When driven by Pr-2, the colour genes showed
marked differences in expression and growth and were therefore not ideally
suited to our purposes. We therefore created versions of the colour genes
that each used the popular registry RBS, B0034. Although the LacI and TetR
RBSes were never directly compared, they both functioned adequately in
subsequent experiments.
Figure 1: Information of RBS protein parts
Figure 2. the list of promoters that were used in our project to regulate and
tune colour expression.1. Promoters Pr-1 to Pr-5 are variants of the Anderson promoters J23114,
J23105, J23108 J23100 and J23119 (wt) that are described in the Registry.
The five bp between the AvrII and NheI sites have been varied to minimize
recombination events when used in combination. Strength refers to the
original fluorescence measurements made using RFP as a reporter. Note that
each promoter is roughly double the strength of the one that follows it in
the list. Pr-0 is a negative control sequence that was designed from the complement of the sequence of Pr-1. The sequences for Tet-Pr, Lac-Pr and lCI-Pr are
as originally reported in Cox et. Al (Molecular systems Biology 2007) where
each operator sequence has been placed between the -35 and -10 regions. The downstream region indicated for each promoter is discussed below.
Promoter DNA used in plasmid constructions was made by annealing plus and
minus strand synthetic oligonucleotides (IDT). 2. Status indicates “made (+)/tested (+)/functional (+) as the best-case scenario. In our hands Pr-5 (wt) failed to produce viable colonies with RFP but worked when linked to LacI This may explain the N.D. result reported for its J23119 analog since strong colour development seems to be associated with slow growth.