The team managed to gather sequences in the registry and modified them in order to improve a) purification and b) could be used in Lactobacillus rhamnosus species; since the registry contains mainly E. coli parts, it might be useful as well, to design and obtain sequences that can be expressed on one or the other but both. The following sequences were codon optimized for use in the previous microorganisms mentioned.
Difference between revisions of "Team:TecMonterrey GDL/Improve"
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| − | <p>The team managed to gather sequences in the registry and modified them in order to improve a) purification and b) could be used in Lactobacillus rhamnosus species; since the registry contains mainly | + | <p>The team managed to gather sequences in the registry and modified them in order to improve a) purification and b) could be used in <i>Lactobacillus rhamnosus</i> species; since the registry contains mainly |
E. coli parts, it might be useful as well, to design and obtain sequences that can be expressed on one or the other but both. | E. coli parts, it might be useful as well, to design and obtain sequences that can be expressed on one or the other but both. | ||
The following sequences were codon optimized for use in the previous microorganisms mentioned.</p> | The following sequences were codon optimized for use in the previous microorganisms mentioned.</p> | ||
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| − | <img class="img-responsive" style=" | + | <img class="img-responsive" style="display: inline" src="https://static.igem.org/mediawiki/2018/4/43/T--TecMonterrey_GDL--Improve--2.png" alt="service-image"> |
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<p>We managed to test some of these pieces when characterizing our signal peptide for secretion of | <p>We managed to test some of these pieces when characterizing our signal peptide for secretion of | ||
| − | recombinant proteins collection | + | recombinant proteins collection <a href="https://2018.igem.org/Team:TecMonterrey_GDL/Parts">Parts</a> and we obtained the following results: </p> |
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Revision as of 00:56, 18 October 2018
Improvement of parts
We managed to test some of these pieces when characterizing our signal peptide for secretion of recombinant proteins collection Parts and we obtained the following results:
