Team:Heidelberg/RFCs

From 2013.igem.org

(Difference between revisions)
Line 18: Line 18:
  </p>
  </p>
-
                 <center><a href="http://dspace.mit.edu/bitstream/handle/1721.1/81333/BBFRFC100.pdf?sequence=1"><button type="button" class="btn btn-default btn-lg">Dowload our RFC 100</button></a></center>
+
                 <center><a href="http://dspace.mit.edu/bitstream/handle/1721.1/81333/BBFRFC100.pdf?sequence=1" target="_blank"><button type="button" class="btn btn-default btn-lg">Dowload our RFC 100</button></a></center>
                 </div>
                 </div>
             </div>
             </div>
Line 25: Line 25:
  <div class="col-sm-12" style="text-align:center" id="rfc99">
  <div class="col-sm-12" style="text-align:center" id="rfc99">
                   <img src="https://static.igem.org/mediawiki/2013/3/37/Heidelberg_RFC99_Pic.png" style="width:100%">
                   <img src="https://static.igem.org/mediawiki/2013/3/37/Heidelberg_RFC99_Pic.png" style="width:100%">
-
                 <a href="http://dspace.mit.edu/bitstream/handle/1721.1/81332/BBFRFC99.pdf?sequence=1"><center><button type="button" class="btn btn-default btn-lg">Dowload our RFC 99</button></center></a>
+
                 <a href="http://dspace.mit.edu/bitstream/handle/1721.1/81332/BBFRFC99.pdf?sequence=1" target="_blank"><center><button type="button" class="btn btn-default btn-lg">Dowload our RFC 99</button></center></a>
                 </div>
                 </div>

Revision as of 13:03, 28 October 2013

RFC 100: Standard for Synthesis of Customized Peptides by Non-Ribosomal Peptide Synthetases

With this RFC, we introduce a standardized framework for the production of short synthetic peptides by engineering customizable non-ribosomal peptide synthetases (NRPS). The framework consists of the NRPSDesigner, a software tool for the in silico design of user-defined NRPSs, a platform for standardized cloning and expression of NRPSs in different bacterial hosts (please refer to our RFC 99 below) and a quality control procedure for the easy validation of NRP production.

Our framework seeks to overcome the two major challenges present in the synthetic peptides field today: making peptide production flexible and scalable at the same time. Chemical peptide synthesis is flexible and enables the incorporation of non-proteinogenic amino acids. However, it is relatively expensive and often uneconomical when used for large-scale peptide production. In contrast, producing recombinant peptides may be cheaper, but their composition is mostly restricted to only 22 different building blocks.

RFC 100 combines the advantages of chemical and recombinant peptide synthesis: it enables the incorporation of hundreds of non-proteinogenic amino acids into the synthetic peptides and is at the same time easily scalable and thus applicable for industrial peptide production. Thus it highly facilitates the production of peptide-based antibiotics, detoxifying agents or chelators applicable for recycling of precious metals from electronic waste. We believe, that RFC 100 represents not only a great foundational advance in the synthetic peptide production field but could become the gold standard for recombinant peptide production in the synthetic biology community.

Thanks to