Difference between revisions of "Part:BBa K2201200"

Revision as of 22:44, 24 September 2017

Tyrosyl tRNA/aminoacyl-synthetase for the incorporation of 2-nitrophenylalanine

To get the noncanonical amino acid 2-nitrophenylalanine (2-NPA) incorporated into a protein auch as the fusion protein of K2201321, a sequence with a TAG is needed along with an additional tRNA synthetase (RS) that is able to load the ncAA to the tRNA. The ribosome is then able to incorporate this amino acid at an amber codon if the target protein with the amber codon and a plasmid with the 2NPA-RS and tRNA are co-transformed. This part contains a promotor for the 2-NPA-RS and the coding sequence for the RS. Additionally, it contains the promoter for the CUA-tRNA and the tRNA sequence itself followed by a terminator.

Figure 1: Plasmid map of the BioBrick K2201200 coding for a 2-NPA-tRNA-synthetasis system based on the ONBY-Part (K1416000). The ONBY-RS was removed by PCR and then a gene synthesis containing the 2-NPA-RS and matching overlaps sides was integrated through Gibson assembly.

We created this specific aaRS by ordering a gene synthesis at Integrated DNA Technologies (IDT) with a codon optimized sequence of an aaRS able to incorporate 2-NPA based on an evolution experiment of Peters et al [3]. This gene synthesis was integrated into the ONBY-Part K1416000 replacing the ONBY-RS. This approach is applicable, as the 2-NPA-RS and the ONBY-RS are mutated versions of the M. jannaschii TyrRS, such that both recognize the same tRNA and only the sequence of the aaRS itself has to be changed to get a new synthetase binding other amino acids to the tRNA. The gene synthesis we ordered had 30 base pairs overlap to a linearized vector of the ONBY-part K1416000, where only the gene sequence of the ONBY-RS was removed. The fragment of the NPA-RS was integrated through Gibson assembly.

Figure 2: History of the plasmid construction of K2201200.

In that specific evolution experiment, ten amino acids in the TyrRS were randomly mutated, resulting in six clones with good incorporation properties for 2-NPA. The best one displayed fidelity rates of approximately 95%. Therefore, its sequence was used for our gene synthesis [3]. Below is a comparison of the mutated amino acid sequences of the M. jannaschii TyrRS, the ONBY-RS and the 2-NPA-RS (table 1).

Table 1: Comparison of the mutated amino acids of the ONBY-RS and 2-NPA-RS to the native Tyr-RS of M. jannaschii.

Tyr-RS Tyr32 Leu65 Ala67 His70 Phe108 Gln109 Tyr114 Asp158 Ile159 Leu162 ONBY-RS Gly Gly Ala His Glu Gln Tyr Ser Ile Glu 2-NPA-RS Gly His Gly Gly Leu Ser Ser Thr Tyr Asp

To proof that the 2-NPA-RS is expressed when E.coli is transformed with this BioBrick, we made a SDS-Page with the cell lysate of a preculture containing this part. The expected molecular weight of our synthetase is 34.76 kDa with an isoelectric point of 6.23. As seen in Figure 3, the SDS-Page shows that the 2-NPA-RS is well expressed in the E.coli strain BL21(DE3) when transformed with the BioBrick.

Sequence and Features