Difference between revisions of "Part:BBa K2201411:Experience"
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===Applications of BBa_K2201411=== | ===Applications of BBa_K2201411=== | ||
| − | We designed and cloned this part to generate a tRNA/synthetase which is able to incorporate 2-Nitro-L-phnylalanine, used for the photocleaving of the polypeptide backbone. | + | We designed and cloned this part to generate a tRNA/synthetase based on the <i>Methanococcus jannashii</i> wild type tyrosyl-tRNA/aminoacyl synthetase, which is able to incorporate 2-Nitro-L-phnylalanine, used for the photocleaving of the polypeptide backbone. |
| − | The library was generated by using two primers, one with nine randomized position (NNK), which are designed to form a dimer. This dimer is completed to a dsDNA by the Klenow fragment. As optical control, a mRFP is incorporated in this certain position to be ranomized, which is then replaced by the dsDNA. | + | The tyrosyl-tRNA/aminoacyl synthetase (TyrRS) is inserted in pSB1C3. The TyrRS library was generated by using two primers, one with nine randomized position (NNK), which are designed to form a dimer. This dimer is completed to a dsDNA by the Klenow fragment. As optical control, a mRFP is incorporated in this certain position to be ranomized, which is then replaced by the dsDNA. |
| − | [[File:T--Bielefeld-CeBiTec--Parts library generation.jpg| | + | [[File:T--Bielefeld-CeBiTec--Parts_library_plasmid.jpg|400px|thumb|right| pSB1C3 backbone, TyrRS (based on <i>Methanocoocs jannashii </i> TyrRS) library plasmid. Depicted without the optical controle]] |
| + | [[File:T--Bielefeld-CeBiTec--Parts library generation.jpg|400px|thumb|right|Generating the library by using randomized primers, forming a dimer, in combination with an optical control <html> <a href="https://parts.igem.org/wiki/index.php?title=Part:(BBa_K2201400)"> (BBa_K2201400) </a> </html>]] | ||
We cloned the library using Gibson Assembly, after transformation we platet them out on LB-plates with chloramphenicol. Altogether, we received more than 130,000 colonies. In evidence due to th optical controle of the template used for the not randomized TyrRS plasmid backbone, we could easily determine the negative colonies. As depicted in Figure 1, 48 of 1310 colonies approximately did not contain the randomized TyrRS library plasmid. Extrapolating this data, we received approximately 125,236.64 library plasmids out of 130,000 colonies, showing a cloning efficiency of 96,34 %, offering a wide diversity of different TyrRS variants. | We cloned the library using Gibson Assembly, after transformation we platet them out on LB-plates with chloramphenicol. Altogether, we received more than 130,000 colonies. In evidence due to th optical controle of the template used for the not randomized TyrRS plasmid backbone, we could easily determine the negative colonies. As depicted in Figure 1, 48 of 1310 colonies approximately did not contain the randomized TyrRS library plasmid. Extrapolating this data, we received approximately 125,236.64 library plasmids out of 130,000 colonies, showing a cloning efficiency of 96,34 %, offering a wide diversity of different TyrRS variants. | ||
| + | |||
| + | [[File:T--Bielefeld-CeBiTec--Parts TyrRS LibraryPlate.jpg|400px|thumb|left|Example of our TyrRS library containing the optical control, platet out on LB plates with chloramphenicol.]] | ||
| + | [[File:T--Bielefeld-CeBiTec--Parts_Sanger_sequencing.jpg|400px|thumb|right|Sanger sequencing of our TyrRS library, showing nine positions, randomized by the use of the NNK scheme. All nucleotides are presented at these positions.]] | ||
We cloned a library of more than 130,000 clones, including more than <b>27,672</b> different TyrRS variants out of 32,768 possible sequence variants, analyzed with MiSeq, Illumina next generation sequencing. These sequences code for more than 8,787 different peptides. | We cloned a library of more than 130,000 clones, including more than <b>27,672</b> different TyrRS variants out of 32,768 possible sequence variants, analyzed with MiSeq, Illumina next generation sequencing. These sequences code for more than 8,787 different peptides. | ||
| − | We used this TyrRS library as a basis to select an tRNA/aminoacyl synthetase pair, able to incorporate 2-Nitrop-L-phenylalanine. Therefore we used our selection system, consisting of a positive (BBa_K2201900) and negative selection plasmid (BBa_K2201901). | + | We used this TyrRS library as a basis to select an tRNA/aminoacyl synthetase pair, able to incorporate 2-Nitrop-L-phenylalanine. Therefore we used our selection system, consisting of a positive <html> <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2201900"> (BBa_K2201900) </a> </html> and negative selection plasmid <html> <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2201901"> (BBa_K2201901) </a> </html>. |
===User Reviews=== | ===User Reviews=== | ||
Revision as of 16:56, 1 November 2017
This experience page is provided so that any user may enter their experience using this part.
Please enter
how you used this part and how it worked out.
Applications of BBa_K2201411
We designed and cloned this part to generate a tRNA/synthetase based on the Methanococcus jannashii wild type tyrosyl-tRNA/aminoacyl synthetase, which is able to incorporate 2-Nitro-L-phnylalanine, used for the photocleaving of the polypeptide backbone.
The tyrosyl-tRNA/aminoacyl synthetase (TyrRS) is inserted in pSB1C3. The TyrRS library was generated by using two primers, one with nine randomized position (NNK), which are designed to form a dimer. This dimer is completed to a dsDNA by the Klenow fragment. As optical control, a mRFP is incorporated in this certain position to be ranomized, which is then replaced by the dsDNA.
We cloned the library using Gibson Assembly, after transformation we platet them out on LB-plates with chloramphenicol. Altogether, we received more than 130,000 colonies. In evidence due to th optical controle of the template used for the not randomized TyrRS plasmid backbone, we could easily determine the negative colonies. As depicted in Figure 1, 48 of 1310 colonies approximately did not contain the randomized TyrRS library plasmid. Extrapolating this data, we received approximately 125,236.64 library plasmids out of 130,000 colonies, showing a cloning efficiency of 96,34 %, offering a wide diversity of different TyrRS variants.
We cloned a library of more than 130,000 clones, including more than 27,672 different TyrRS variants out of 32,768 possible sequence variants, analyzed with MiSeq, Illumina next generation sequencing. These sequences code for more than 8,787 different peptides.
We used this TyrRS library as a basis to select an tRNA/aminoacyl synthetase pair, able to incorporate 2-Nitrop-L-phenylalanine. Therefore we used our selection system, consisting of a positive (BBa_K2201900) and negative selection plasmid (BBa_K2201901) .
User Reviews
UNIQ053b794c2dafb9d4-partinfo-00000003-QINU UNIQ053b794c2dafb9d4-partinfo-00000004-QINU