Team:Heidelberg/Parts

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<h1 style="margin-top:10%"><span style="font-size:150%">Our Parts.</span><span style="font-size:90%" class="text-muted"> Fascinating stuff out of the world of non-ribosomal peptides.</span></h1>
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<h1><span style="font-size:150%; color:#666666">Our Parts.</span><span style="font-size:90%" class="text-muted"> Now it is Your turn. Start working with NRPS!</span></h1>
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                   <h2 id="TeamParts">Team Parts</h2>
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Our favorite part is <a href="http://parts.igem.org/Part:BBa_K1152007">BBa_K1152007</a>: Helper construct for NRP-Indigoidine-tagging.
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<li> Highly efficient (i.e. 0 % false-positive rate) cloning due to negative selection with ccdB.
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<li> Compatibility with custom non-ribosomal peptide (NRP) synthesis.
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<li> Optimized fusion of the NRP to Indigoidine that serves as a tag that eases detection of positive clones that synthesize the desired construct.
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                   <h2><span style="font-size:170%;">Synthetic Peptides</span style="font-size:170%;"> - <span style="font-size":50%">BBa_K1152000 - 2005</h2>
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                            We provide the constructs for the novel Dipeptide- and Tripeptide-Synthetases. Furthermore, we submitted the single modules that they are comprised of. These parts should serve as the basis of a future library for standardized work with NRPS. The modules are specific for different amino acids: Phenylalanine (tycA), Proline (tycB1) and Leucine (tycC6).
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                                    <img src="https://static.igem.org/mediawiki/2013/2/26/Heidelberg_Parts_Gallery_1.png" style="width:70%; padding:1%" />
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                  <h2><span style="font-size:170%;">Indigoidine-Tag</span style="font-size:170%;"> - <span style="font-size":50%">BBa_K1152006 & 2007</h2>
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                            One of our major achievements is the establishment of an easily detectable, inert and universal tag - the <a href="https://2013.igem.org/Team:Heidelberg/Project/Indigoidine-Tag">Indigoidine-Tag</a>. With this tag, purification and validation of novel NRPs is significantly eased. The characteristics of the tag compare to those of the GFP-tag for proteins. We submit the helper-construct for tagging any desired Non-Ribosomal Peptide as our <a href="https://2013.igem.org/Team:Heidelberg/Favorite_Parts">favorite part</a>.
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                  <h2><span style="font-size:170%;">Tag-Optimization</span style="font-size:170%;"> - <span style="font-size":50%">BBa_K1152008 & 2013-2019</h2>
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                            Besides establishing the <a href="https://2013.igem.org/Team:Heidelberg/Project/Indigoidine-Tag">Indigoidine-Tag</a>, we focussed on <a href="https://2013.igem.org/Team:Heidelberg/Project/Tag-Optimization">optimizing</a> its functionality and efficiency. Therefore, we modified the natural sequence of the Indigoidine synthetase indC (which is our <a href="https://2013.igem.org/Team:Heidelberg/Favorite_Parts">Best Natural BioBrick</a> by domain exchange which lead to altered and in some cases enhanced efficiency of the NRP-production. We submit the collection of alternate T-domains, of which we created several functional, synthetic ones as <a href="https://2013.igem.org/Team:Heidelberg/Favorite_Parts">Best Part Range</a>.
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                  <h2><span style="font-size:170%;">Tag-Characterization</span style="font-size:170%;"> - <span style="font-size":50%">BBa_K1152009 - 2012</h2>
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                            During <a href="https://2013.igem.org/Team:Heidelberg/Project/Tag-Optimization">Tag-Optimization</a>, we also focussed on the enzymes that are required for the activation of NRPSs - the PPTases. We characterized several PPTases and assessed their compatibility and efficiency. We thereby improved parts <b><a href="http://parts.igem.org/Part:BBa_K802006">BBa_K802006</a></b> and <b><a href="http://parts.igem.org/Part:BBa_K302010">BBa_K302010</a></b> from the registry, which are PPTase-encoding parts not annotated or characterized.
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We propose <a href="http://parts.igem.org/Part:BBa_K1152013">BBa_K1152013</a> as Best new BioBrick Part, Natural, because:
 
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<li> it encodes the original NRPS module from <i>Photorhabdus luminescens</i> capable of synthesizing Indigoidine
 
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<li> the BioBrick can be combined with modules from other NRPSs to yield fusion peptides with a blue pigment tag
 
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<li> standardization and established protocols allow for BioBrick assembly or Gibson assembly
 
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We propose <a href="http://parts.igem.org/Part:BBa_K1152007">BBa_K1152007</a> as Best new BioBrick Part or Device, Engineered, as mentioned above.
 
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We propose <a href="http://parts.igem.org/Part:BBa_K1152009">BBa_K1152009</a> as Most Improved Registry Part, because:
 
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<li> it encodes for sfp, a 4'-Phosphopanthetheinyl-transferase (PPTase) crucial for the activation of T domains
 
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<li> it improved the parts <a href="http://parts.igem.org/Part:BBa_K802006">BBa_K802006</a> and <a href="http://parts.igem.org/Part:BBa_K302010">BBa_K302010</a>, which do also encode for sfp from <i>Bacillus subtilis</i> but were deviating in three amino acids from the sequence published on <a href="http://www.ncbi.nlm.nih.gov/">NCBI</a>
 
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<li> it is the first BioBrick in the registry that is explicitly encoding sfp, and it is annotated and characterized
 
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We propose <a href="http://parts.igem.org/Part:BBa_K1152015">BBa_K1152015</a>, <a href="http://parts.igem.org/Part:BBa_K1152016">BBa_K1152016</a>, <a href="http://parts.igem.org/Part:BBa_K1152017">BBa_K1152017</a>, <a href="http://parts.igem.org/Part:BBa_K1152018">BBa_K1152018</a>, <a href="http://parts.igem.org/Part:BBa_K1152019">BBa_K1152019</a>, <a href="http://parts.igem.org/Part:BBa_K1152020">BBa_K1152020</a> as Best Part Collection, because:
 
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<li>they represent a valuable ensemble of various T domains with different properties
 
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<li>they were designed semi-rationally based on multiple sequence alignments
 
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<li>they exhibit distinct synthesis rates for Indigoidine depending on the T domains of this part collection
 
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<h2><span style="font-size:170%;">List of Parts</span style="font-size:170%;"> - <span style="font-size":50%">BBa_K1152000 - 2019</h2>
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<h3 id="PartList">List of all submitted parts:</h3>
 
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Latest revision as of 21:57, 28 October 2013

Our Parts. Now it is Your turn. Start working with NRPS!


Synthetic Peptides - BBa_K1152000 - 2005

We provide the constructs for the novel Dipeptide- and Tripeptide-Synthetases. Furthermore, we submitted the single modules that they are comprised of. These parts should serve as the basis of a future library for standardized work with NRPS. The modules are specific for different amino acids: Phenylalanine (tycA), Proline (tycB1) and Leucine (tycC6).



Indigoidine-Tag - BBa_K1152006 & 2007

One of our major achievements is the establishment of an easily detectable, inert and universal tag - the Indigoidine-Tag. With this tag, purification and validation of novel NRPs is significantly eased. The characteristics of the tag compare to those of the GFP-tag for proteins. We submit the helper-construct for tagging any desired Non-Ribosomal Peptide as our favorite part.



Tag-Optimization - BBa_K1152008 & 2013-2019

Besides establishing the Indigoidine-Tag, we focussed on optimizing its functionality and efficiency. Therefore, we modified the natural sequence of the Indigoidine synthetase indC (which is our Best Natural BioBrick by domain exchange which lead to altered and in some cases enhanced efficiency of the NRP-production. We submit the collection of alternate T-domains, of which we created several functional, synthetic ones as Best Part Range.



Tag-Characterization - BBa_K1152009 - 2012

During Tag-Optimization, we also focussed on the enzymes that are required for the activation of NRPSs - the PPTases. We characterized several PPTases and assessed their compatibility and efficiency. We thereby improved parts BBa_K802006 and BBa_K302010 from the registry, which are PPTase-encoding parts not annotated or characterized.




List of Parts - BBa_K1152000 - 2019

Thanks to

Retrieved from "http://2013.igem.org/Team:Heidelberg/Parts"